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French Survey About Student's Sleep Perturbations Before Simulation Session.

French National Investigation About Student's Sleep Perturbations Before Simulation Session.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02922608
Acronym
Simsleep
Enrollment
1150
Registered
2016-10-04
Start date
2016-10-31
Completion date
2017-12-01
Last updated
2018-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Sleep

Keywords

Education, Medical

Brief summary

High fidelity simulation provide educational skills but the simulation of critical events could eventually provide anxiety among participants. 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.

Detailed description

High fidelity simulation provide educational skills but the simulation of critical events could eventually provide anxiety among participants. 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.

Interventions

OTHERsimulation practice

simulation session

Sponsors

Claude Bernard University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* french talking residents coming to high fidelity simulation

Exclusion criteria

* refusal to participate

Design outcomes

Primary

MeasureTime frame
modification of the sleeping Leeds testday 1

Secondary

MeasureTime frame
incidence of sleep perturbationsday 1
analysis of demographics and sleep perturbationsday 1

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026