ClinicalTrials.Veeva

Menu

Relaxation Before Debriefing and Memorization in High Fidelity Simulation in Healthcare (RELAXSIMHF)

C

Claude Bernard University

Status

Completed

Conditions

Anxiety

Treatments

Behavioral: relaxation

Study type

Interventional

Funder types

Other

Identifiers

NCT02470130
CLESS 2014

Details and patient eligibility

About

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.

Full 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.

Enrollment

150 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 4 patient groups

relax actor
Active Comparator group
Description:
actor during simulation and relaxation before debriefing
Treatment:
Behavioral: relaxation
no relax actor
No Intervention group
Description:
actor during simulation and no relaxation before debriefing
relax observer
Active Comparator group
Description:
observer during simulation and relaxation before debriefing
Treatment:
Behavioral: relaxation
no relax observer
No Intervention group
Description:
observer during simulation and no relaxation before debriefing

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems