- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06952972
MorphECOS - Evaluation of the Influence of Fatigue and Sleep on the Performance of 2nd Cycle Medical Students (OSCE) (MorphECOS)
MorphECOS - Evaluation of the Influence of Fatigue and Sleep on the Performance of 2nd Cycle Medical Students (OSCE): a Single-centre Observational Study
Objective and Structured Clinical Examinations (OSCEs) has been incorporated recently in the certification process as a final national undergraduate ranking examination. This exam is a challenge for medical students.
The aim of this study is to better characterise the population of students taking the OSCEs on the subject of sleep and fatigue and to assess whether these factors have an impact on their performance in the OSCEs.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Lyon, France, 69003
- Claude Bernard University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Subjects of legal age, enrolled in the 2nd cycle médical program at the Lyon Est Faculty of Medicine (Claude Bernard Lyon 1 University), taking part in the annual session (February or March 2025) of the faculty's OSCEs and having agreed to participate by completing and signing the dedicated written consent form.
Exclusion Criteria:
- abstenteism or Premature end to the OSCE session.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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5th year of medical curriculum
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6th year of medical curriculum
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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PERFORMANCE
Time Frame: obtained seven days after the objectif structured clinical examination
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Score at the objectif structured clinical examination exam from 0 minimum to 200 points maximum
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obtained seven days after the objectif structured clinical examination
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Significant difference in student performance per station and per item
Time Frame: obtained seven days after the objectif structured clinical examination
|
Significant difference in student performance per station and per item
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obtained seven days after the objectif structured clinical examination
|
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Significant difference in Visual Analog Scale response according to the different profiles
Time Frame: Two times : 1 hour before and 1 hour after the OSCE session
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Significant difference in Visual Analog Scale response according to the different profiles
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Two times : 1 hour before and 1 hour after the OSCE session
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Collaborators and Investigators
Sponsor
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- MorphECOS
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
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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