Relaxation Before Debriefing and Memorization in High Fidelity Simulation in Healthcare

NCT ID: NCT02470130

Last Updated: 2016-07-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2016-03-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Anxiety

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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relax actor

actor during simulation and relaxation before debriefing

Group Type ACTIVE_COMPARATOR

relaxation

Intervention Type BEHAVIORAL

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

no relax actor

actor during simulation and no relaxation before debriefing

Group Type NO_INTERVENTION

No interventions assigned to this group

relax observer

observer during simulation and relaxation before debriefing

Group Type ACTIVE_COMPARATOR

relaxation

Intervention Type BEHAVIORAL

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

no relax observer

observer during simulation and no relaxation before debriefing

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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relaxation

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

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Claude Bernard University

OTHER

Sponsor Role lead

Responsible Party

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Lilot Marc

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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jean jacques Lehot, PHD

Role: STUDY_CHAIR

HCL

Locations

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CLESS

Lyon, Auvergne-Rhône-Alpes, France

Site Status

Countries

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France

Other Identifiers

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CLESS 2014

Identifier Type: -

Identifier Source: org_study_id

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