French Survey About Student's Sleep Perturbations Before Simulation Session.
NCT ID: NCT02922608
Last Updated: 2018-01-25
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
1150 participants
OBSERVATIONAL
2016-10-31
2017-12-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The anxiety could raise before the simulation session and affect the perceived quality of sleep the night prior to the simulation session. The lack of sleep would eventually affect both participation and memorization during the simulation session. The investigators would like to investigate with a survey how much participants had their sleep affected before the simulation session.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Study of Effects of Light on the Vigilance and Cognitive Performance Following a Night Without Sleep
NCT02478528
Impaired Vigilance, and Its Effects on Cognition and Behavior
NCT02484846
Sleep for Optimal MEdical StudentS (PROMESS)
NCT06297330
Impact of Sleep Workshops in College Students
NCT02665247
Sleep and Memory in Children
NCT02785328
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The anxiety could raise before the simulation session and affect the perceived quality of sleep the night prior to the simulation session. The lack of sleep would eventually affect both participation and memorization during the simulation session.
The investigators would like to investigate with a survey how much participants had their quantity and quality of sleep affected before the simulation session.
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
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
simulation practice
simulation session
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
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.
Lilot Marc
MD
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
jean-jacques lehot, PHD
Role: STUDY_CHAIR
Cless
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CLESS
Lyon, Auvergne-Rhône-Alpes, 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.
simusleepsurvey
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.