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Clinical Trial Summary

The purpose of this study was to analyze the correlation between the resilience of anesthesia professionals and the stress measured during a simulation session.


Clinical Trial Description

This trial will be carried out at the simulation center of the training institute for health professionals of the CHU Grenoble Alpes. Volunteer anesthesia professionals and students will perform a scenario simulating a pediatric laryngospasm during a surgical incision. Each scenario will be performed by a medical and paramedical anesthesia pair and supervised by simulation trainers. Stress and resilience measures will be taken at various times during the study. Participants will be debriefed at the end of the simulation. The primary objective is to analyze the correlation between anesthesia professionals' resilience and measured stress.Secondary objectives are to study the association between: SDNN-measured stress and VAS-reported stress, age and SDNN-measured stress, CD RISC 10 resilience and PSS10-reported stress, CD RISC resilience and VAS-reported stress, the effect of experience on SDNN-measured stress, multiple correlation of the different secondary criteria. secondary criteria. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05073445
Study type Observational
Source University Hospital, Grenoble
Contact
Status Completed
Phase
Start date June 18, 2021
Completion date November 15, 2021

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