An observational study in Stress, Professional, Resilience and Anaesthesiology, sponsored by University Hospital, Grenoble. Completed at 1 site in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-03-18.
Sponsored by University Hospital, Grenoble · Observational
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.
236 studies on the registry are indexed under Occupational Stress; 64 are open to participants now.
This study's enrollment of 34 is below the median of 200 across 64 observational studies indexed under Occupational Stress.
Browse Occupational Stress studies →University Hospital, Grenoble is the lead sponsor of 815 studies on the registry; 205 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Anaesthetic teams composed with :
Exclusion Criteria:
SDNN measurement during pediatric simulation
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
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)
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 debriefing (at 30 minutes)
Perceived Stress Scale
The Perceived Stress Scale (PSS10 from 10 To 50) measures the degree to which respondents feel their lives are unpredictable, uncontrollable, and overloaded. A high score indicates more stress.
Time frame: 5 days before scenario
Age of anesthesia professionals
Age of anesthesia professionals: (quantitative variable)
Time frame: 5 days before scenario
Experience in anesthesia:
Experience in anesthesia: number of years since the beginning of specialized training training (quantitative variable)
Time frame: 5 days before scenario
Pediatric experience:
Pediatric experience: qualitative variable (yes, no)
Time frame: 5 days before scenario
Pediatric laryngospasm experience
Pediatric laryngospasm experience: qualitative variable: (yes, no)
Time frame: 5 days before scenario
Heart rate variability
Standard deviation of the average of RR intervals (SDNN in milliseconds) in participants
Time frame: 5 days before scenario (during 3 minutes)
Heart rate variability
Standard deviation of the average of RR intervals (SDNN in milliseconds) in participants
Time frame: Before the scenario (during 3 minutes)
Heart rate variability
Standard deviation of the average of RR intervals (SDNN in milliseconds) in participants
Time frame: during briefing (during 3 minutes at 0 minutes)
Heart rate variability
Standard deviation of the average of RR intervals (SDNN in milliseconds) in participants
Time frame: during the scenario before the laryngospasm (during 3 minutes at 3 minutes)
Heart rate variability
Standard deviation of the average of RR intervals (SDNN in milliseconds) in participants
Time frame: during the debriefing (3 minutes at 9 minutes)
Heart rate variability
Standard deviation of the average of RR intervals (SDNN in milliseconds) in participants
Time frame: after the debriefing (3 minutes at 30 minutes)
This study is completed, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.
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University Hospital, Grenoble