N95 Reuse During COVID-19 (ReuseN95)

A Clinical Examination of N95 Reuse and Extended Use

During critical personal protective equipment (PPE) shortages, such as those associated with the COVID-19 pandemic, Centers for Disease Control (CDC) recommends N95 extended use (wearing the same N95 for multiple patient encounters) and limited reuse (storing an N95 between shifts for use over multiple shifts with or without decontamination) as contingency and crisis capacity strategies, respectively. Many healthcare workers (HCWs) are employing these strategies out of necessity. The sustained performance of these respirators depends on the respirator maintaining its filtration efficiency and its ability to provide an adequate seal (fit) to the user's face. Fit testing is performed when a respirator is issued to the user and on an annual basis thereafter. A user-seal check is then performed whenever a respirator is donned. Previous studies have found repeated donnings/doffings to significantly decrease the respirator's fit. A recent pilot cross-sectional clinical study conducted by the University of California, San Francisco found fit failures of respirators after being worn for 2 shifts. However, more definitive data regarding respirator performance during reuse and extended use are lacking. The investigators plan to address these critical gaps in knowledge by conducting a prospective cohort study to determine the incidence of N95 fit failure when subjected to extended use/reuse in a clinical setting. The investigators plan to enroll 396 ED providers (including physicians, nurses, and staff) when obtaining a new NIOSH approved N95s and performing serial fit tests at the end of each 8-12 hour shift for up to 5 clinical shifts or until N95 failure, whichever is earlier. By carefully measuring fit test failure in a clinical setting, the investigators will be able to provide guidance regarding the safety of N95 extended use and reuse necessitated by the need for PPE conservation. Specifically, the investigators will address the following research questions: 1) how long N95s maintain their fit during extended use, 2) how many times N95s can be donned/doffed and maintain their fit, 3) the ability of a user seal check to indicate fit in the field, 4) what adverse health effects, reports of discomfort, or symptoms are experienced by users during extended use and reuse, 5) what effect does extended use and reuse have on N95 filtration performance, 6) the level of contamination of N95s when subjected to extended use and reuse, 7) the effect of modifications to N95 (covering an N95 with a face shield or surgical N95s, facial coverings) on fit failure.

Study Overview

• Status: Completed
• Conditions: Emergency Medicine; Healthcare Worker; Frontline Providers

Detailed Description

Frontline healthcare workers are at high risk of SARS (severe acute respiratory syndrome) CoV-2 (COVID-19) infection. Personal protective equipment (PPE), such as an N95 respirator (N95), is essential for prevention of COVID-19 among HCWs. N95s can prevent aerosolized transmission of viral particles and reduce COVID-19 among HCWs, helping to reduce infection rates and preserve the workforce. Under normal circumstances, the CDC recommends that HCWs dispose of N95s after a single patient encounter. However, during critical PPE shortages such as those during the current COVID-19 pandemic, the CDC recommends N95 extended use (wearing the same N95 for multiple patient encounters) and re-use (storing an N95 between shifts for use over multiple shifts). N95 shortages have been widely reported during the COVID-19 pandemic and have forced HCWs to practice extended use and reuse of N95s. Despite the CDC's guidelines, there are limited data regarding the efficacy of N95s under conditions of extended use and reuse and existing studies have been conducted in laboratory settings rather than in the actual health care environment. (Bergman 2012; Vuma et al 2019). This has left health care workers, including emergency department (ED) providers on the front lines of the COVID-19 pandemic, without clear guidance regarding N95 conservation. Many have implemented various reuse and extended use policies out of necessity but with no empirical evidence of their safety and effectiveness.

The study team conducted a pilot cross-sectional study of 68 ED providers who wore either a 3M 1860 dome style N95 or a duckbill N951. 70.6% of duckbill N95 failed a standardized fit test with 3M bitter solution and a hood. Of the dome style , 27.5% failed a fit test. N95 failure was associated with increasing numbers of shifts used: There were 0/11 failures after 1 shift, 1/12 failures after 2 shifts, 3/13 failures after 3 shifts, and 10/15 failures after 4 or more shifts. Also, more donnings and doffings were associated with fit failure, with a median of 8 donning and doffings in the fit pass group and 15 donning and doffings in the fit failure group. This preliminary study had a number of limitations, including a small sample size, convenience sampling, and cross-sectional design, and so was unable to definitively identify the number of shifts or donnings/doffings for which N95s can be safely reused.

The investigators propose to conduct a prospective cohort study of 396 participants across 6 ED sites to estimate the cumulative incidence of N95s when subjected to extended use and reuse in a clinical (emergency department) setting with fit test failure and contamination as the main endpoints. The investigators also seek to compare the fit test failure between varying types of HCWs wearing a number of N95 types. Additionally, the investigators will collect the N95s used in this study for additional analyses of at an outside laboratory measuring COVID-19 contamination levels and filtration efficiency.

• Study Type: Observational
• Enrollment (Actual): 412

Contacts and Locations

Study Locations

• United States
  • California
    • San Francisco, California, United States, 94143
      • University of California, San Francisco

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

• Sampling Method: Probability Sample

Study Population

Healthcare provider, specifically frontline workers that involves direct patient contact.

Description

Inclusion criteria

• Adult (18 years old or greater)
• ED providers (MDs, nurses, Advanced Practice Providers (APPs)) who are practicing extended use and re-use for the majority (more than half) of their shifts Participants are eligible when obtaining a new N95 and are scheduled to work a minimum of 5 shifts within a 60-day period. As hours of enrollment and data collection depend on research associate availability, participants working certain shifts may not be eligible.

Exclusion criteria:

• Participant does not intend to use N95 for majority of shift
• Schedule prohibits re-use and or data collection
• Repeated failed baseline fit test
• Refused or unable to consent
• Pregnant
• Facial hair (e.g., beards or sideburns) or jewelry which interferes with the face seal region of an N95

Study Plan

How is the study designed?

Design Details

• Observational Models: Cohort
• Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of participants with qualitative fit test failure (N95 A, end of shift 1)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 1, for N95 A. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift A1, up to 12 hours
Number of participants with qualitative fit test failure (N95 A, end of shift 2)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 2, for N95 A. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift A2, up to 12 hours per shift, 24 hours maximum
Number of participants with qualitative fit test failure (N95 A, end of shift 3)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 3, for N95 A. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift A3, up to 12 hours per shift, 36 hours maximum
Number of participants with qualitative fit test failure (N95 A, end of shift 4)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 4, for N95 A. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift A4, up to 12 hours per shift, 48 hours maximum
Number of participants with qualitative fit test failure (N95 A, end of shift 5)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 5, for N95 A. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift A5, up to 12 hours per shift, 60 hours maximum
Number of participants with qualitative fit test failure (N95 B, end of shift 1)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 1, for N95 B. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift B1, up to 12 hours maximum
Number of participants with qualitative fit test failure (N95 B, end of shift 2)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 2, for N95 B. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift B2, up to 12 hours per shift, 24 hours maximum
Number of participants with qualitative fit test failure (N95 B, end of shift 3)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 3, for N95 B. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift B3, up to 12 hours per shift, 36 hours maximum
Number of participants with qualitative fit test failure (N95 B, end of shift 4)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 4, for N95 B. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift B4, up to 12 hours per shift, 48 hours maximum
Number of participants with qualitative fit test failure (N95 B, end of shift 5)	Qualitative fit test outcome is measured by a trained fit tester at the end of participant shift 5, for N95 B. The fit test is performed up to 5 times per N95 or until fit test failure. The fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no).	At the end of shift B5, up to 12 hours per shift, 60 hours maximum

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of participants with User Seal Check failure (N95 A, end of shift 1)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given facial filtering respirator (FFR) develops an acceptable "leak-free" seal with a subject's face. A user seal check (USC) is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research Clinical Research Coordinator (CRC) will record whether the user seal check indicates a good seal.	At the end of shift A1, up to 12 hours maximum
Number of participants with User Seal Check failure (N95 A, end of shift 2)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift A2, up to 12 hours per shift, 24 hours maximum
Number of participants with User Seal Check failure (N95 A, end of shift 3)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift A3, up to 12 hours per shift, 36 hours maximum
Number of participants with User Seal Check failure (N95 A, end of shift 4)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift A4, up to 12 hours per shift, 48 hours maximum
Number of participants with User Seal Check failure (N95 A, end of shift 5)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift A5, up to 12 hours per shift, 60 hours maximum
Number of participants with User Seal Check failure (N95 B, end of shift 1)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift B1, up to 12 hours maximum
Number of participants with User Seal Check failure (N95 B, end of shift 2)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift B2, up to 12 hours per shift, 24 hours maximum
Number of participants with User Seal Check failure (N95 B, end of shift 3)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift B3, up to 12 hours per shift, 36 hours maximum
Number of participants with User Seal Check failure (N95 B, end of shift 4)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift B4, up to 12 hours per shift, 48 hours maximum
Number of participants with User Seal Check failure (N95 B, end of shift 5)	Participants will be asked to perform a brief "self- test" occurring prior to an actual fit test to determine that a given FFR develops an acceptable "leak-free" seal with a subject's face. A USC is subjective and determines whether the participant feels that the respirator seals well enough with the participant's face to proceed forward with the actual fit test. The research CRC will record whether the user seal check indicates a good seal.	At the end of shift B5, up to 12 hours per shift, 60 hours maximum

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of participants with qualitative fit test failure of Mask A (at Baseline)	Qualitative fit test outcome for Mask A is measured by a trained fit tester prior to study inclusion. For each of the 2 N95s, the fit tester records whether the N95 passed fit testing (Yes or No). The fit test variable outcome indicates a passed fit test (yes) or failed fit test (no). Only passed N95s may continue into the study. Failed mask details (manufacturer, lot number, expiration date) are collected for analysis.	Prior to study inclusion
N95 B Outcome	N95 Qualitative Fit Test Outcome is measured over a maximum of 5 study shifts per N95. An Study N95s B can have 1 of 3 outcomes: (1) Passed all 5 fit tests, (2) Failed before 5 fit tests, or (3) Experienced Competing Event. N95s that either pass all 5 fit tests or experience a competing event which precludes the N95 from being fit tested will be censored in Kaplan Meier curve analysis.	Within 6 months of enrollment
N95 A Outcome	N95 Qualitative Fit Test Outcome is measured over a maximum of 5 study shifts per N95. A Study N95s A can have 1 of 3 outcomes: (1) Passed all 5 fit tests, (2) Failed before 5 fit tests, or (3) Experienced Competing Event. N95s that either pass all 5 fit tests or experience a competing event which precludes the N95 from being fit tested will be censored in Kaplan Meier curve analysis.	Within 6 months of enrollment
N95 contamination as measured by Real-time Quantitative Polymerase Chain Reaction (RTqPCR) for COVID-19 (to be assessed by collecting masks and sending out to lab)	Each N95 labeled 'Mask A' which fails or is censored (completes 5 shifts or experiences competing event) will be collected in a sealable plastic storage container, stored, and shipped to Applied Research Associates.	At the end of all study shifts, up to 10 visits (60 hours maximum).
N95 filtration as measured using TSI 8130, measuring flow rate (ml/min), particle penetration (%), and pressure drop (mmH2O).	Each N95 labeled 'Mask B' which fails or is censored (completes 5 shifts or experiences competing event) will be collected in a sealable plastic storage container, stored, and shipped to Applied Research Associates.	At the end of all study shifts, up to 10 visits (60 hours maximum).
Participant reported symptoms (comfort)	The investigators will collect data on participant reported outcomes, including symptoms from survey of participants at end of each shift, using the validated R-COMFI scale to measure mask discomfort.	At the end of each shift, up to 12 hours
Number of N95 donnings and doffings for Mask A during shift 1 (N95 A, end of shift 1)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift A1, up to 12 hours maximum
Number of N95 donnings and doffings for Mask A during shift 2 (N95 A, end of shift 2)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift A2, up to 12 hours per shift, 24 hours maximum
Number of N95 donnings and doffings for Mask A during shift 3 (N95 A, end of shift 3)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift A3, up to 12 hours per shift, 36 hours maximum
Number of N95 donnings and doffings for Mask A during shift 4 (N95 A, end of shift 4)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift A4, up to 12 hours per shift, 48 hours maximum
Number of N95 donnings and doffings for Mask A during shift 5 (N95 A, end of shift 5)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift A5, up to 12 hours per shift, 60 hours maximum
Number of N95 donnings and doffings for Mask B during shift 1 (N95 B, end of shift 1)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift B1, up to 12 hours
Number of N95 donnings and doffings for Mask B during shift 2 (N95 B, end of shift 2)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift B2, up to 12 hours
Number of N95 donnings and doffings for Mask B during shift 3 (N95 B, end of shift 3)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift B3, up to 12 hours
Number of N95 donnings and doffings for Mask B during shift 4 (N95 B, end of shift 4)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift B4, up to 12 hours
Number of N95 donnings and doffings for Mask B during shift 5 (N95 B, end of shift 5)	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	At the end of shift B5, up to 12 hours
Number of total N95 donnings and doffings for Mask A during shifts 1-5	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	Cumulative donning/doffing for up to 5 shifts, up to 12 hours each shift.
Number of total N95 donnings and doffings for Mask B during shifts 1-5	When a mask is removed and replaced on the face to be worn, participants will count 1 "donning & doffing".	Cumulative donning/doffing for up to 5 shifts, up to 12 hours each shift.
Shift Length (N95 A, end of shift 1)	Length of participant's shift in hours.	At the end of shift A1, up to 12 hours per shift.
Shift Length (N95 A, end of shift 2)	Length of participant's shift in hours.	At the end of shift A2, up to 12 hours per shift.
Shift Length (N95 A, end of shift 3)	Length of participant's shift in hours.	At the end of shift A3, up to 12 hours per shift.
Shift Length (N95 A, end of shift 4)	Length of participant's shift in hours.	At the end of shift A4, up to 12 hours per shift.
Shift Length (N95 A, end of shift 5)	Length of participant's shift in hours.	At the end of shift A5, up to 12 hours per shift.
Shift Length (N95 B, end of shift 1)	Length of participant's shift in hours.	At the end of shift B1, up to 12 hours per shift.
Shift Length (N95 B, end of shift 2)	Length of participant's shift in hours.	At the end of shift B2, up to 12 hours per shift.
Shift Length (N95 B, end of shift 3)	Length of participant's shift in hours.	At the end of shift B3, up to 12 hours per shift.
Shift Length (N95 B, end of shift 4)	Length of participant's shift in hours.	At the end of shift B4, up to 12 hours per shift.
Shift Length (N95 B, end of shift 5)	Length of participant's shift in hours.	At the end of shift B5, up to 12 hours per shift.
Cumulative Shift Length (N95 A)	Total length of participant's shifts in hours.	Up to 5 shifts, up to 12 hours per shift.
Cumulative Shift Length (N95 B)	Total length of participant's shifts in hours.	Up to 5 shifts, up to 12 hours per shift.
Estimated Hours Worn (N95 A, end of shift 1)	Participants will estimate the total hours the N95 was worn.	At the end of shift A1, up to 12 hours per shift.
Estimated Hours Worn (N95 A, end of shift 2)	Participants will estimate the total hours the N95 was worn.	At the end of shift A2, up to 12 hours per shift.
Estimated Hours Worn (N95 A, end of shift 3)	Participants will estimate the total hours the N95 was worn.	At the end of shift A3, up to 12 hours per shift.
Estimated Hours Worn (N95 A, end of shift 4)	Participants will estimate the total hours the N95 was worn.	At the end of shift A4, up to 12 hours per shift.
Estimated Hours Worn (N95 A, end of shift 5)	Participants will estimate the total hours the N95 was worn.	At the end of shift A5, up to 12 hours per shift.
Estimated Hours Worn (N95 B, end of shift 1)	Participants will estimate the total hours the N95 was worn.	At the end of shift B1, up to 12 hours per shift.
Estimated Hours Worn (N95 B, end of shift 2)	Participants will estimate the total hours the N95 was worn.	At the end of shift B2, up to 12 hours per shift.
Estimated Hours Worn (N95 B, end of shift 3)	Participants will estimate the total hours the N95 was worn.	At the end of shift B3, up to 12 hours per shift.
Estimated Hours Worn (N95 B, end of shift 4)	Participants will estimate the total hours the N95 was worn.	At the end of shift B4, up to 12 hours per shift.
Estimated Hours Worn (N95 B, end of shift 5)	Participants will estimate the total hours the N95 was worn.	At the end of shift B5, up to 12 hours per shift.
Cumulative Estimated Hours Worn (N95 A)	Participants will estimate the total hours the N95 was worn.	Total estimated hours worn for up to 5 shifts, up to 12 hours per shift.
Cumulative Estimated Hours Worn (N95 B)	Participants will estimate the total hours the N95 was worn.	Total estimated hours worn for up to 5 shifts, up to 12 hours per shift.
Tightness of Straps, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Tightness of Straps, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Tightness of Straps, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Tightness of Straps, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Tightness of Straps, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Tightness of Straps, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Tightness of Straps, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Tightness of Straps, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Tightness of Straps, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Tightness of Straps, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to tightness of straps during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Facial Irritation, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Facial Irritation, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Facial Irritation, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Facial Irritation, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Facial Irritation, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Facial Irritation, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Facial Irritation, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Facial Irritation, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Facial Irritation, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Facial Irritation, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial irritation (leaves marks/indents) during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Facial Itching, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Facial Itching, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Facial Itching, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Facial Itching, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Facial Itching, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Facial Itching, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Facial Itching, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Facial Itching, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Facial Itching, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Facial Itching, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial itching during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Facial Pinching, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Facial Pinching, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Facial Pinching, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Facial Pinching, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Facial Pinching, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Facial Pinching, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Facial Pinching, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Facial Pinching, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Facial Pinching, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Facial Pinching, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial pinching during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Nose, nose-bridge (pinching, redness from metal band), B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nose and nose-bridge pinching/redness from metal band during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Facial Heat/Warmth, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Facial Heat/Warmth, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Facial Heat/Warmth, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Facial Heat/Warmth, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Facial Heat/Warmth, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Facial Heat/Warmth, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Facial Heat/Warmth, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Facial Heat/Warmth, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Facial Heat/Warmth, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Facial Heat/Warmth, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to facial heat/warmth during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Sweat/Moisture buildup, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Sweat/Moisture buildup, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Sweat/Moisture buildup, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Sweat/Moisture buildup, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Sweat/Moisture buildup, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Sweat/Moisture buildup, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Sweat/Moisture buildup, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Sweat/Moisture buildup, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Sweat/Moisture buildup, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Sweat/Moisture buildup, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to sweat/moisture buildup during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Lack of Fresh Air, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Lack of Fresh Air, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Lack of Fresh Air, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Lack of Fresh Air, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Lack of Fresh Air, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Lack of Fresh Air, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Lack of Fresh Air, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Lack of Fresh Air, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Lack of Fresh Air, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Lack of Fresh Air, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to lack of fresh air during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Nausea, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Nausea, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Nausea, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Nausea, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Nausea, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Nausea, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Nausea, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Nausea, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Nausea, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Nausea, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to nausea during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Headache, A1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Headache, A2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Headache, A3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Headache, A4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Headache, A5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Headache, B1	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Headache, B2	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Headache, B3	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Headache, B4	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Headache, B5	Level of N95 discomfort as measured by how often wearing the fit-tested filtering face-piece respirator caused discomfort due to headache during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Dizziness, A1	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Dizziness, A2	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Dizziness, A3	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Dizziness, A4	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Dizziness, A5	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Dizziness, B1	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Dizziness, B2	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Dizziness, B3	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Dizziness, B4	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Dizziness, B5	Qualitative experience of wearing N95 as measured by participant reporting dizziness during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Loss of energy/tiredness/fatigue, A1	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Loss of energy/tiredness/fatigue, A2	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Loss of energy/tiredness/fatigue, A3	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Loss of energy/tiredness/fatigue, A4	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Loss of energy/tiredness/fatigue, A5	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Loss of energy/tiredness/fatigue, B1	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Loss of energy/tiredness/fatigue, B2	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Loss of energy/tiredness/fatigue, B3	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Loss of energy/tiredness/fatigue, B4	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Loss of energy/tiredness/fatigue, B5	Qualitative experience of wearing N95 as measured by participant reporting loss of energy/tiredness/fatigue during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Claustrophobia, A1	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Claustrophobia, A2	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Claustrophobia, A3	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Claustrophobia, A4	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Claustrophobia, A5	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Claustrophobia, B1	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Claustrophobia, B2	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Claustrophobia, B3	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Claustrophobia, B4	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Claustrophobia, B5	Qualitative experience of wearing N95 as measured by participant reporting claustrophobia during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Shortness of Breath, A1	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Shortness of Breath, A2	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Shortness of Breath, A3	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Shortness of Breath, A4	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Shortness of Breath, A5	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Shortness of Breath, B1	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Shortness of Breath, B2	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Shortness of Breath, B3	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Shortness of Breath, B4	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Shortness of Breath, B5	Qualitative experience of wearing N95 as measured by participant reporting shortness of breath during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Difficulty Breathing, A1	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Difficulty Breathing, A2	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Difficulty Breathing, A3	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Difficulty Breathing, A4	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Difficulty Breathing, A5	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Difficulty Breathing, B1	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Difficulty Breathing, B2	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Difficulty Breathing, B3	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Difficulty Breathing, B4	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Difficulty Breathing, B5	Qualitative experience of wearing N95 as measured by participant reporting difficulty breathing during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Dry or Itchy Eyes, A1	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift A1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A1, up to 12 hours
Dry or Itchy Eyes, A2	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift A2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A2, up to 12 hours
Dry or Itchy Eyes, A3	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift A3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A3, up to 12 hours
Dry or Itchy Eyes, A4	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift A4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A4, up to 12 hours
Dry or Itchy Eyes, A5	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift A5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift A5, up to 12 hours
Dry or Itchy Eyes, B1	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift B1. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B1, up to 12 hours
Dry or Itchy Eyes, B2	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift B2. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B2, up to 12 hours
Dry or Itchy Eyes, B3	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift B3. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B3, up to 12 hours
Dry or Itchy Eyes, B4	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift B4. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B4, up to 12 hours
Dry or Itchy Eyes, B5	Qualitative experience of wearing N95 as measured by participant reporting dry or itchy eyes during shift B5. R-COMFI scaled variable with three potential outcomes, in order of increasing severity: none of the time, some of the time, all of the time.	At the end of shift B5, up to 12 hours
Concentration, A1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift A1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A1, up to 12 hours
Concentration, A2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift A2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A2, up to 12 hours
Concentration, A3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift A3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A3, up to 12 hours
Concentration, A4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift A4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A4, up to 12 hours
Concentration, A5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift A5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A5, up to 12 hours
Concentration, B1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift B1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B1, up to 12 hours
Concentration, B2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift B2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B2, up to 12 hours
Concentration, B3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift B3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B3, up to 12 hours
Concentration, B4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift B4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B4, up to 12 hours
Concentration, B5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask affected my concentration while working (always adjusting the mask)" during shift B5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B5, up to 12 hours
Verbally Communicate, A1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift A1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A1, up to 12 hours
Verbally Communicate, A2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift A2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A2, up to 12 hours
Verbally Communicate, A3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift A3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A3, up to 12 hours
Verbally Communicate, A4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift A4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A4, up to 12 hours
Verbally Communicate, A5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift A5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A5, up to 12 hours
Verbally Communicate, B1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift B1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B1, up to 12 hours
Verbally Communicate, B2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift B2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B2, up to 12 hours
Verbally Communicate, B3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift B3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B3, up to 12 hours
Verbally Communicate, B4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift B4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B4, up to 12 hours
Verbally Communicate, B5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficulty verbally communicating to others (unintelligible, muffled speech)" during shift B5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B5, up to 12 hours
Hearing, A1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift A1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A1, up to 12 hours
Hearing, A2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift A2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A2, up to 12 hours
Hearing, A3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift A3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A3, up to 12 hours
Hearing, A4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift A4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A4, up to 12 hours
Hearing, A5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift A5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A5, up to 12 hours
Hearing, B1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift B1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B1, up to 12 hours
Hearing, B2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift B2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B2, up to 12 hours
Hearing, B3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift B3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B3, up to 12 hours
Hearing, B4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift B4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B4, up to 12 hours
Hearing, B5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "I had difficultly hearing others" during shift B5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B5, up to 12 hours
Obstructed Vision, A1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift A1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A1, up to 12 hours
Obstructed Vision, A2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift A2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A2, up to 12 hours
Obstructed Vision, A3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift A3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A3, up to 12 hours
Obstructed Vision, A4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift A4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A4, up to 12 hours
Obstructed Vision, A5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift A5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A5, up to 12 hours
Obstructed Vision, B1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift B1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B1, up to 12 hours
Obstructed Vision, B2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift B2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B2, up to 12 hours
Obstructed Vision, B3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift B3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B3, up to 12 hours
Obstructed Vision, B4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift B4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B4, up to 12 hours
Obstructed Vision, B5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask obstructed my vision" during shift B5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B5, up to 12 hours
Interfered Care, A1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift A1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A1, up to 12 hours
Interfered Care, A2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift A2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A2, up to 12 hours
Interfered Care, A3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift A3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A3, up to 12 hours
Interfered Care, A4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift A4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A4, up to 12 hours
Interfered Care, A5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift A5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift A5, up to 12 hours
Interfered Care, B1	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift B1. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B1, up to 12 hours
Interfered Care, B2	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift B2. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B2, up to 12 hours
Interfered Care, B3	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift B3. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B3, up to 12 hours
Interfered Care, B4	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift B4. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B4, up to 12 hours
Interfered Care, B5	Qualitative assessment of N95 functionality as measured by participant reporting their level of agreement with the statement "The mask interfered with my patient care duties (quick to leave room, less interaction)" during shift B5. R-COMFI scaled variable with four potential outcomes, in order of increasing severity: strongly disagree, disagree, agree, strongly agree.	At the end of shift B5, up to 12 hours
Irritated Skin, A1	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift A1.	At the end of shift A1, up to 12 hours
Irritated Skin, A2	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift A2.	At the end of shift A2, up to 12 hours
Irritated Skin, A3	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift A3.	At the end of shift A3, up to 12 hours
Irritated Skin, A4	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift A4.	At the end of shift A4, up to 12 hours
Irritated Skin, A5	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift A5.	At the end of shift A5, up to 12 hours
Irritated Skin, B1	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift B1.	At the end of shift B1, up to 12 hours
Irritated Skin, B2	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift B2.	At the end of shift B2, up to 12 hours
Irritated Skin, B3	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift B3.	At the end of shift B3, up to 12 hours
Irritated Skin, B4	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift B4.	At the end of shift B4, up to 12 hours
Irritated Skin, B5	Assessment of any facial irritation/marks/dents as measured by photographic evidence after shift B5.	At the end of shift B5, up to 12 hours
Facial Thermal Sensation, A1	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift A1 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A1, up to 12 hours
Facial Thermal Sensation, A2	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift A2 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A2, up to 12 hours
Facial Thermal Sensation, A3	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift A3 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A3, up to 12 hours
Facial Thermal Sensation, A4	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift A4 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A4, up to 12 hours
Facial Thermal Sensation, A5	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift A5 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A5, up to 12 hours
Facial Thermal Sensation, B1	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift B1 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B1, up to 12 hours
Facial Thermal Sensation, B2	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift B2 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B2, up to 12 hours
Facial Thermal Sensation, B3	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift B3 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B3, up to 12 hours
Facial Thermal Sensation, B4	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift B4 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B4, up to 12 hours
Facial Thermal Sensation, B5	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their face during shift B5 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B5, up to 12 hours
Body Thermal Sensation, A1	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift A1 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A1, up to 12 hours
Body Thermal Sensation, A2	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift A2 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A2, up to 12 hours
Body Thermal Sensation, A3	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift A3 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A3, up to 12 hours
Body Thermal Sensation, A4	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift A4 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A4, up to 12 hours
Body Thermal Sensation, A5	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift A5 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift A5, up to 12 hours
Body Thermal Sensation, B1	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift B1 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B1, up to 12 hours
Body Thermal Sensation, B2	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift B2 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B2, up to 12 hours
Body Thermal Sensation, B3	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift B3 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B3, up to 12 hours
Body Thermal Sensation, B4	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift B4 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B4, up to 12 hours
Body Thermal Sensation, B5	Qualitative assessment of N95 comfort measured by participant reporting of the thermal sensation of their whole body during shift B5 as very hot, hot, warm, slightly warm, neither warm nor cool, slightly cool, cool, cold, very cold.	At the end of shift B5, up to 12 hours
Aerosolized Generating Procedures, A1	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, cardiopulmonary resuscitation (CPR), respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift A1.	At the end of shift A1, up to 12 hours
Aerosolized Generating Procedures, A2	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift A2.	At the end of shift A2, up to 12 hours
Aerosolized Generating Procedures, A3	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift A3.	At the end of shift A3, up to 12 hours
Aerosolized Generating Procedures, A4	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift A4.	At the end of shift A4, up to 12 hours
Aerosolized Generating Procedures, A5	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift A5.	At the end of shift A5, up to 12 hours
Aerosolized Generating Procedures, B1	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift B1.	At the end of shift B1, up to 12 hours
Aerosolized Generating Procedures, B2	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift B2.	At the end of shift B2, up to 12 hours
Aerosolized Generating Procedures, B3	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift B3.	At the end of shift B3, up to 12 hours
Aerosolized Generating Procedures, B4	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift B4.	At the end of shift B4, up to 12 hours
Aerosolized Generating Procedures, B5	The number of participants who entered rooms with aerosolized generating procedures (intubations, positive pressure ventilation, CPR, respiratory/airway suctioning, nebulizer treatments, nasopharyngeal aspiration) during shift B5.	At the end of shift B5, up to 12 hours
Contact with respiratory/influenza symptoms, A1	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift A1.	At the end of shift A1, up to 12 hours
Contact with respiratory/influenza symptoms, A2	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift A2.	At the end of shift A2, up to 12 hours
Contact with respiratory/influenza symptoms, A3	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift A3.	At the end of shift A3, up to 12 hours
Contact with respiratory/influenza symptoms, A4	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift A4.	At the end of shift A4, up to 12 hours
Contact with respiratory/influenza symptoms, A5	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift A5.	At the end of shift A5, up to 12 hours
Contact with respiratory/influenza symptoms, B1	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift B1.	At the end of shift B1, up to 12 hours
Contact with respiratory/influenza symptoms, B2	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift B2.	At the end of shift B2, up to 12 hours
Contact with respiratory/influenza symptoms, B3	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift B3.	At the end of shift B3, up to 12 hours
Contact with respiratory/influenza symptoms, B4	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift B4.	At the end of shift B4, up to 12 hours
Contact with respiratory/influenza symptoms, B5	The number of participants who were in contact with patients with respiratory symptoms, or influenza like symptoms, while wearing the N95 mask during shift B5.	At the end of shift B5, up to 12 hours
Number of patients with respiratory/influenza symptoms, A1	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift A1.	At the end of shift A1, up to 12 hours
Number of patients with respiratory/influenza symptoms, A2	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift A2.	At the end of shift A2, up to 12 hours
Number of patients with respiratory/influenza symptoms, A3	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift A3.	At the end of shift A3, up to 12 hours
Number of patients with respiratory/influenza symptoms, A4	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift A4.	At the end of shift A4, up to 12 hours
Number of patients with respiratory/influenza symptoms, A5	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift A5.	At the end of shift A5, up to 12 hours
Number of patients with respiratory/influenza symptoms, B1	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift B1.	At the end of shift B1, up to 12 hours
Number of patients with respiratory/influenza symptoms, B2	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift B2.	At the end of shift B2, up to 12 hours
Number of patients with respiratory/influenza symptoms, B3	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift B3.	At the end of shift B3, up to 12 hours
Number of patients with respiratory/influenza symptoms, B4	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift B4.	At the end of shift B4, up to 12 hours
Number of patients with respiratory/influenza symptoms, B5	The number of patients with respiratory symptoms or influenza like symptoms that a participant saw while wearing the N95 mask during shift B5.	At the end of shift B5, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, A1	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift A1.	At the end of shift A1, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, A2	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift A2.	At the end of shift A2, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, A3	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift A3.	At the end of shift A3, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, A4	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift A4.	At the end of shift A4, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, A5	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift A5.	At the end of shift A5, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, B1	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift B1.	At the end of shift B1, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, B2	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift B2.	At the end of shift B2, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, B3	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift B3.	At the end of shift B3, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, B4	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift B4.	At the end of shift B4, up to 12 hours
Estimated duration with patients with respiratory/influenza symptoms, B5	The total estimated duration in minutes of contact between a participant and patients with respiratory symptoms or influenza like symptoms during shift B5.	At the end of shift B5, up to 12 hours
Distance between patients with respiratory/influenza symptoms, A1	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift A1. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift A1, up to 12 hours
Distance between patients with respiratory/influenza symptoms, A2	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift A2. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift A2, up to 12 hours
Distance between patients with respiratory/influenza symptoms, A3	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift A3. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift A3, up to 12 hours
Distance between patients with respiratory/influenza symptoms, A4	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift A4. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift A4, up to 12 hours
Distance between patients with respiratory/influenza symptoms, A5	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift A5. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift A5, up to 12 hours
Distance between patients with respiratory/influenza symptoms, B1	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift B1. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift B1, up to 12 hours
Distance between patients with respiratory/influenza symptoms, B2	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift B2. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift B2, up to 12 hours
Distance between patients with respiratory/influenza symptoms, B3	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift B3. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift B3, up to 12 hours
Distance between patients with respiratory/influenza symptoms, B4	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift B4. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift B4, up to 12 hours
Distance between patients with respiratory/influenza symptoms, B5	The minimum estimated distance between a participant and a patient with respiratory symptoms or influenza like symptoms during shift B5. Scaled variable in order of increasing risk: more than 6ft, less than 6ft, direct contact.	At the end of shift B5, up to 12 hours
COVID-19, A1	The number of participants who were in contact with patients with confirmed COVID-19 during shift A1.	At the end of shift A1, up to 12 hours
COVID-19, A2	The number of participants who were in contact with patients with confirmed COVID-19 during shift A2.	At the end of shift A2, up to 12 hours
COVID-19, A3	The number of participants who were in contact with patients with confirmed COVID-19 during shift A3.	At the end of shift A3, up to 12 hours
COVID-19, A4	The number of participants who were in contact with patients with confirmed COVID-19 during shift A4.	At the end of shift A4, up to 12 hours
COVID-19, A5	The number of participants who were in contact with patients with confirmed COVID-19 during shift A5.	At the end of shift A5, up to 12 hours
COVID-19, B1	The number of participants who were in contact with patients with confirmed COVID-19 during shift B1.	At the end of shift B1, up to 12 hours
COVID-19, B2	The number of participants who were in contact with patients with confirmed COVID-19 during shift B2.	At the end of shift B2, up to 12 hours
COVID-19, B3	The number of participants who were in contact with patients with confirmed COVID-19 during shift B3.	At the end of shift B3, up to 12 hours
COVID-19, B4	The number of participants who were in contact with patients with confirmed COVID-19 during shift B4.	At the end of shift B4, up to 12 hours
COVID-19, B5	The number of participants who were in contact with patients with confirmed COVID-19 during shift B5.	At the end of shift B5, up to 12 hours
Number of COVID-19 patients, A1	The number of patients with confirmed COVID-19 that a participant saw during shift A1.	At the end of shift A1, up to 12 hours
Number of COVID-19 patients, A2	The number of patients with confirmed COVID-19 that a participant saw during shift A2.	At the end of shift A2, up to 12 hours
Number of COVID-19 patients, A3	The number of patients with confirmed COVID-19 that a participant saw during shift A3.	At the end of shift A3, up to 12 hours
Number of COVID-19 patients, A4	The number of patients with confirmed COVID-19 that a participant saw during shift A4.	At the end of shift A4, up to 12 hours
Number of COVID-19 patients, A5	The number of patients with confirmed COVID-19 that a participant saw during shift A5.	At the end of shift A5, up to 12 hours
Number of COVID-19 patients, B1	The number of patients with confirmed COVID-19 that a participant saw during shift B1.	At the end of shift B1, up to 12 hours
Number of COVID-19 patients, B2	The number of patients with confirmed COVID-19 that a participant saw during shift B2.	At the end of shift B2, up to 12 hours
Number of COVID-19 patients, B3	The number of patients with confirmed COVID-19 that a participant saw during shift B3.	At the end of shift B3, up to 12 hours
Number of COVID-19 patients, B4	The number of patients with confirmed COVID-19 that a participant saw during shift B4.	At the end of shift B4, up to 12 hours
Number of COVID-19 patients, B5	The number of patients with confirmed COVID-19 that a participant saw during shift B5.	At the end of shift B5, up to 12 hours
Completed all 5 study visits (N95 A)	Number of N95 A masks that completed all 5 study visits.	At the end of shift A5, up to 60 hours
Completed all 5 study visits (N95 B)	Number of N95 B masks that completed all 5 study visits.	At the end of shift B5, up to 60 hours
Failed before 5 study visits (N95 A)	Number of N95 A masks that failed before 5 study visits.	At the end of shift A1-A5, up to 60 hours
Failed before 5 study visits (N95 B)	Number of N95 B masks that failed before 5 study visits.	At the end of shift B1-B5, up to 60 hours
Competing event (N95 A)	Number of N95 A masks which could not be fit tested due to a competing event (lost, soiled, damaged, etc).	Between shifts A1-A5, up to 60 hours
Competing event (N95 B)	Number of N95 B masks which could not be fit tested due to a competing event (lost, soiled, damaged, etc).	Between shifts B1-B5, up to 60 hours

Collaborators and Investigators

• Sponsor: University of California, San Francisco
• Collaborators: Johns Hopkins University; University of California, San Diego; University of Wisconsin, Madison; Emory University; Centers for Disease Control and Prevention; University of Rochester

Study record dates

Study Major Dates

• Study Start (Actual): April 1, 2021
• Primary Completion (Actual): December 31, 2022
• Study Completion (Actual): December 31, 2022

Study Registration Dates

• First Submitted: December 6, 2021
• First Submitted That Met QC Criteria: December 6, 2021
• First Posted (Actual): December 8, 2021

Study Record Updates

• Last Update Posted (Estimate): February 16, 2023
• Last Update Submitted That Met QC Criteria: February 15, 2023
• Last Verified: February 1, 2023

More Information

Terms related to this study

• Keywords: Personal Protective Equipment; N95 mask; Extended use; reuse
• Additional Relevant MeSH Terms: Pathologic Processes; Disease Attributes; Emergencies
• Other Study ID Numbers: 21-33232

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: The investigators will not share individual participant data.

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No