MorphECOS - Evaluation of the Influence of Fatigue and Sleep on the Performance of 2nd Cycle Medical Students (OSCE)
NCT ID: NCT06952972
Last Updated: 2025-05-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
619 participants
OBSERVATIONAL
2025-01-27
2025-03-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Sleep for Optimal MEdical StudentS (PROMESS)
NCT06297330
Effect of a Sleep Hygiene-based Intervention on Sleep Quality and Mental Health in Medical Students
NCT07043530
Cognitive Performance After a Night Shift in Internal Medicine Residents
NCT04053556
Optimizing Sleep/Wake Related Cognitive Efficacy
NCT02412410
Effects of Time of Sleep Restriction in Obesity
NCT01259895
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
5th year of medical curriculum
5th year of medical curriculum
No interventions assigned to this group
6th year of medical curriculum
6th year of medical curriculum
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Claude Bernard University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Evan GOUY
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Claude Bernard University
Lyon, France, France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
MorphECOS
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.