- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03439683
KAP Asynchrony Survey (KAPA)
Knowledge, Attitudes And Practices Among Critical Care Professionals Towards Patient-Ventilator Asynchrony
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Juliana C Ferreira, MD
- Phone Number: +5511983355876
- Email: juliana.ferreira@hc.fm.usp.br
Study Contact Backup
- Name: Mayson L Sousa, RRT
- Phone Number: +5511985519000
- Email: mayson.laercio@hc.fm.usp.br
Study Locations
-
-
SP
-
Sao Paulo, SP, Brazil, 05403010
- Recruiting
- Hospital das Clínicas -HCFMUSP
-
Contact:
- Juliana C Ferreira, MD
- Phone Number: +5511983355876
-
Principal Investigator:
- juliana ferreira, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- current working in the ICU as a physician, nurse or respiratory therapist
Exclusion Criteria:
- refusal to sign informed consent
- incomplete survey (less than 80% of the questions answered)
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Physicians
Definition: Physicians working in the ICU for at least 50% of their time in the hospital Intervention: Survey about patient-ventilator asynchrony |
Participants will fill an online survey that asks multiple-choice questions related to knowledge, attitudes and practice related to patient-ventilator asynchrony and also have images of ventilator waveforms wth asynchrony, where they need to identify the type of asynchrony
|
Nurses
Definition: Nurses working in the ICU for at least 20 hours/week Intervention: Survey about patient-ventilator asynchrony |
Participants will fill an online survey that asks multiple-choice questions related to knowledge, attitudes and practice related to patient-ventilator asynchrony and also have images of ventilator waveforms wth asynchrony, where they need to identify the type of asynchrony
|
Respiratory Therapists
Definition: Respiratory Therapists working in the ICU for at least 20 hours/week Intervention: Survey about patient-ventilator asynchrony |
Participants will fill an online survey that asks multiple-choice questions related to knowledge, attitudes and practice related to patient-ventilator asynchrony and also have images of ventilator waveforms wth asynchrony, where they need to identify the type of asynchrony
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Survey score
Time Frame: in 30 minutes (at survey completion)
|
the number of correct answers given to knowledge part of the survey
|
in 30 minutes (at survey completion)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
attitudes score
Time Frame: in 30 minutes (at survey completion)
|
the number of desirable answers given to attitudes part of the survey
|
in 30 minutes (at survey completion)
|
Practice score
Time Frame: in 30 minutes (at survey completion)
|
the number of desirable answers given to practice part of the survey
|
in 30 minutes (at survey completion)
|
Collaborators and Investigators
Investigators
- Principal Investigator: JULIANA C FERREIRA, MD, University of Sao Paulo
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 61472716.1.0000.0068
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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