NCT05073445 - Stress and Resilience in Anesthesia Professionals | Crick

Overview

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

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 Type

OBSERVATIONAL

Enrollment

34

Conditions

Stress, Professional Resilience Anaesthesiology High Fidelity Simulation

Interventions

SDNN measurementBEHAVIORAL

SDNN measurement during pediatric simulation

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: \- volunteer in anesthesia Exclusion Criteria: * Rhythm disorders * Endocrine pathology * High blood pressure * Pregnancy or breastfeeding in progress * Taking anti-inflammatory or psychotropic drugs that interfere with the heart rate * Interruption of professional practice in anesthesia \> 2 years

Locations (1)

University Hospital

Grenoble, France

Outcomes

Primary Outcomes

Heart rate variability

Standard deviation of the average of RR intervals (SDNN in milliseconds) in participants

Time frame: during the laryngospasm (during 3 minutes at 6 minutes)

Resilience

Measurement of resilience by Connor-Davidson Resilience Scale 10 (CD RISC 10 from 0 to 40) in participants. A high score indicates better resilience.

Time frame: 5 days before scenario

Secondary Outcomes

Self-reported stress

Stress level self reported by participants on visual analogical scale (VAS from 0 to 100); One end of the scale represents the maximum conceivable symptom strength (i. e., 100%), the other end no symptoms whatsoever (i. e., 0%).

Time frame: 5 days before scenario

Self-reported stress

Stress level self reported by participants on visual analogical scale (VAS from 0 to 100); One end of the scale represents the maximum conceivable symptom strength (i. e., 100%), the other end no symptoms whatsoever (i. e., 0%).

Time frame: just Before the scenario (at 0 minute )

Self-reported stress

Stress level self reported by participants on visual analogical scale (VAS from 0 to 100); One end of the scale represents the maximum conceivable symptom strength (i. e., 100%), the other end no symptoms whatsoever (i. e., 0%).

Time frame: just after briefing (at 3 minutes)

Self-reported stress

Stress level self reported by participants on visual analogical scale (VAS from 0 to 100); One end of the scale represents the maximum conceivable symptom strength (i. e., 100%), the other end no symptoms whatsoever (i. e., 0%).

Time frame: just after the end of scenario (at 9 minutes)