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NCT06078631 Clinical Trial

Influence of Students Behaviors on Performance and Quality of Life on the OSCE

Performance Anxiety Clinical Trial

— ECOPERF  

Official title:
Influence of Students Behaviors on Thier Performance and Quality of Life on the OSCE

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06078631
Other study ID # ECOPERF1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 5, 2023
Est. completion date August 11, 2024

Study information
Verified date June 2024
Source Claude Bernard University
Contact Sophie Schlatter, PhD
Phone 0651806521
Email sophie.schlatter@univ-lyon1.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The students behave differentially before an exam. 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.

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).

Recruitment information / eligibility
Status Recruiting
Enrollment 500
Est. completion date August 11, 2024
Est. primary completion date August 5, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility 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 Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Marc lilot Lyon

Sponsors (1)
Lead Sponsor Collaborator
Claude Bernard University

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary PERFORMANCE Score at the OSCE exam from 0 to 40 points obtained 7 days after the OSCE
Secondary SF-12 Overall quality of life obtained one hour after the OSCE
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