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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02470130
Other study ID # CLESS 2014
Secondary ID
Status Completed
Phase N/A
First received May 20, 2015
Last updated July 5, 2016
Start date October 2014
Est. completion date March 2016

Study information

Verified date July 2016
Source Claude Bernard University
Contact n/a
Is FDA regulated No
Health authority France: Ethics Committee
Study type Interventional

Clinical Trial Summary

Resident in advanced medical training participated to high fidelity simulation education program in Lyon. Alternatively 1 or 2 resident act during a scenario while the others observe in a teletransmission closeby room. Debriefing follows the critical scenario in witch resident are involved. The investigators are testing the effects of five minute of conversational relaxation before the debriefing on the anxiety level and memorization of key points each scénario on participant and observer.


Description:

Resident in advanced medical training participated to high fidelity simulation education program in Lyon. This is part of a curriculum and each year they go throw a specific simulation session in groups of 3 to 8 residents with same specific thematic education goals. 3 to 4 differents scénario are run every simulation session during 4 to 5 hours, every day 2 similar session are run with 2 different groups of same level residents. Alternatively 1 or 2 resident act during a scenario while the others observe in a teletransmission room. Debriefing follows the critical scenario in witch resident are involved. The investigators are testing the effects of five minute of conversational relaxation before the debriefing on the anxiety level and memorization of key points each scénario on participant and observer. Relaxation is done reading a text outloud by an instructor before the debriefing. Each scenario is run in the morning and the afternoon and alternatively have relaxation or not. evaluation is done on participant of the scenario and resident observer of the situation. The Investigators ask participant for demographic data, anxiety scale test, multiple anxiety visual analogic scale. At the end of every scenario 5 clinical key point of teh scenario are exposed. At 3 month the investigators call back every participant to ask them to remember these 5 points for the scenario they were involved in and one of the other they observed.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- every resident going to a scheduled simulation session part of the normal education program of the residency.

Exclusion Criteria:

- no consent, or consent deleted

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
relaxation
5 min of conversational relaxation red by one of the instructor between simulation and debriefing

Locations

Country Name City State
France CLESS Lyon Rhône-Alpes

Sponsors (1)

Lead Sponsor Collaborator
Claude Bernard University

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary memorization of the active scenario 5 key points for the resolution of the scenario, 1 point per key points recalled by the participant, metrics from 0 to 5. 3 month No
Secondary anxiety visual analog scale : metrics from 0 to 100 mm min 1 No
Secondary debriefing score of quality of the debriefing questionnaire of 6 items quoted, total score from 25 to 175 min 1 No
Secondary observing visual analog scale : metrics from 0 to 100 mm min 1 No
Secondary memorization of the passive scenario 5 key points for the resolution of the scenario, 1 point per key points recalled by the participant, metrics from 0 to 5. 3 month No
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