Stress and Resilience in Anesthesia Professionals
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Stress, Professional
- Sponsor
- University Hospital, Grenoble
- Enrollment
- 34
- Locations
- 1
- Primary Endpoint
- Resilience
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief 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.
Detailed 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.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Resilience
Time Frame: 5 days before scenario
Measurement of resilience by Connor-Davidson Resilience Scale 10 (CD RISC 10 from 0 to 40) in participants. A high score indicates better resilience.
Heart rate variability
Time Frame: during the laryngospasm (during 3 minutes at 6 minutes)
Standard deviation of the average of RR intervals (SDNN in milliseconds) in participants
Secondary Outcomes
- Experience in anesthesia:(5 days before scenario)
- Pediatric experience:(5 days before scenario)
- Age of anesthesia professionals(5 days before scenario)
- Self-reported stress(just after the debriefing (at 30 minutes))
- Perceived Stress Scale(5 days before scenario)
- Pediatric laryngospasm experience(5 days before scenario)
- Heart rate variability(after the debriefing (3 minutes at 30 minutes))