- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06078631
Influence of Students Behaviors on Performance and Quality of Life on the OSCE (ECOPERF)
Influence of Students Behaviors on Thier Performance and Quality of Life on the OSCE
Study Overview
Status
Detailed Description
The students behave differentially before an exam. They can be discriminate, on their sleeping, coping, or physical activity behavior. They also show difference in the number of hours they study by weeks or if they use the services offer by their university.
This study aims at determining the influence of all these behaviors on the perceived quality of life of students and their performance during their OSCE (a major exam).
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Lyon, France, 69003
- Marc lilot
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- all volontary medical students of the third cycle that came for their exam during the sessions of December and May 2023 from the University of Lyon (Medecine ESt)
Exclusion Criteria:
- no exclusion criteria
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PERFORMANCE
Time Frame: obtained 7 days after the OSCE
|
Score at the OSCE exam from 0 to 40 points
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obtained 7 days after the OSCE
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
SF-12
Time Frame: obtained one hour after the OSCE
|
Overall quality of life
|
obtained one hour after the OSCE
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Gilles Rode, PhD, UCBL1
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
- ECOPERF1
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
product manufactured in and exported from the U.S.
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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