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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02922608
Recruitment Status : Completed
First Posted : October 4, 2016
Last Update Posted : January 25, 2018
Sponsor:
Information provided by (Responsible Party):
Lilot Marc, Claude Bernard University

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.


Condition or disease Intervention/treatment
Sleep Anxiety Other: simulation practice

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.

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Study Type : Observational
Actual Enrollment : 1150 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: French National Investigation About Student's Sleep Perturbations Before Simulation Session.
Study Start Date : October 2016
Actual Primary Completion Date : December 1, 2017
Actual Study Completion Date : December 1, 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Anxiety


Intervention Details:
  • Other: simulation practice
    simulation session


Primary Outcome Measures :
  1. modification of the sleeping Leeds test [ Time Frame: day 1 ]

Secondary Outcome Measures :
  1. incidence of sleep perturbations [ Time Frame: day 1 ]
  2. analysis of demographics and sleep perturbations [ Time Frame: day 1 ]


Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
residents coming to simulation center for high fidelity simulation education program.
Criteria

Inclusion Criteria:

  • french talking residents coming to high fidelity simulation

Exclusion Criteria:

  • refusal to participate

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02922608


Locations
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France
CLESS
Lyon, Rhône-Alpes, France, 69007
Sponsors and Collaborators
Claude Bernard University
Investigators
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Study Chair: jean-jacques lehot, PHD Cless

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Responsible Party: Lilot Marc, MD, Claude Bernard University
ClinicalTrials.gov Identifier: NCT02922608    
Other Study ID Numbers: simusleepsurvey
First Posted: October 4, 2016    Key Record Dates
Last Update Posted: January 25, 2018
Last Verified: January 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
Keywords provided by Lilot Marc, Claude Bernard University:
Education, Medical