- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04783688
Evaluation of Full Face Snorkel Masks (FFSMs)
Evaluation of a Full Face Snorkel Mask (FFSM)
Study Overview
Status
Intervention / Treatment
Detailed Description
The scientific testing will take place in the water tank of Foxtrot chamber at the Duke Center for Hyperbaric Medicine & Environmental Physiology. This Center (referred to as "Duke Hyperbarics") has a long history of testing various aspects of undersea physiology and causes of injury and death. Duke Hyperbarics will conduct the physical tests, and DAN (Divers Alert Network) personnel will also supervise the scientific testing.
The experimental test subjects will be divided into two categories. Before testing, both categories will come in for a screening day, where they will go through the informed consent process and be medically screened for safety to perform activity. For the first category of subjects (Group A), five volunteer subjects will be recruited with no restrictions on age or fitness level. An effort will be made to include representative test subjects from older age ranges (>35 years old) in this group. To ensure they can safely perform light activity, they will be screened for cardiovascular disease, both by questionnaire and by a physical exam during the screening day.
The second group (Group B) will be age 18-40, non-smoking, and screened for fitness using a physical exam and a VO2max test. The reason for these two groups is to ensure that a spectrum of test subjects is examined across the comprehensive range of ages and fitness levels that may participate in snorkeling as recreation.
The testing will be designed to assess the function of the FFSMs produced by multiple brands compared to each other as well as compared to conventional snorkels. Test subjects will be positioned horizontally in warm water. They will be face-down on a bicycle ergometer, grasping handlebars for stability. On the test day, each subject will undergo three test procedures, using first a conventional snorkel then two different brands of FFSM while pedaling the underwater bicycle. Group A will be asked to pedal at a rate that is comfortable for them, while Group B will be given a targeted higher work rate to achieve.
For each FFSM test, the test subject will be asked to place the mask on themselves but provided no further instruction. The pressure exerted by the mask on the forehead will also be measured by placing a small, flexible, force-sensitive gauge between the skirt and the skin (this gauge needs to be in place for only a few seconds and will be removed before snorkeling). At the end of each test, the subjects will be asked to remove the FFSM quickly in response to an audible or visual alarm that will appear three times at randomized intervals. Their ability to remove the masks quickly will be timed.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
North Carolina
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Durham, North Carolina, United States, 27710
- Duke University Center for Hyperbaric Medicine & Environmental Physiology
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Genders Eligible for Study
Description
GROUP A:
Inclusion Criteria:
- Preferred >35 years old
- Safe to perform light activity
Exclusion Criteria:
- Subjects must NOT be certified SCUBA divers
GROUP B:
Inclusion Criteria:
- Age 18-40
- VO2max exercise test results >30 mL/kg/min for female, >35 mL/kg/min for male
Exclusion Criteria:
- Subjects must NOT be certified SCUBA divers
- May not be active smokers
Study Plan
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Experimental Group
All subjects will snorkel using the same FFSMs.
|
A mask used for snorkeling that covers the entire face, as opposed to a conventional snorkel, which is held in the mouth only.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fractional level of oxygen in the breathing gas (at steady state) provided by the different mask models
Time Frame: Estimated 4 hours long
|
The breathing gas provided to the snorkeler by the masks will be measured continuously throughout the experiment using a mass spectrometer.
|
Estimated 4 hours long
|
|
Fractional level of carbon dioxide in the breathing gas (at steady state) provided by the different mask models
Time Frame: Estimated 4 hours long
|
The breathing gas provided to the snorkeler by the masks will be measured continuously throughout the experiment using a mass spectrometer.
|
Estimated 4 hours long
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speed of removal of the different FFSM models
Time Frame: Estimated 20 minutes
|
The speed at which subjects can remove the different models of FFSM will be timed and measured in seconds for comparison between models.
|
Estimated 20 minutes
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Rachel Lance, PhD, Duke University Health System, Department of Anesthesiology
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Pro00106241
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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