Stress and Resilience in Anesthesia Professionals

NCT ID: NCT05073445

Last Updated: 2022-03-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

34 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-06-18

Study Completion Date

2021-11-15

Brief Summary

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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

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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.

Conditions

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Stress, Professional Resilience Anaesthesiology High Fidelity Simulation

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Interventions

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SDNN measurement

SDNN measurement during pediatric simulation

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Yoann Zafiriou

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Grenoble

Julien Picard, M.D, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Grenoble

Locations

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University Hospital

Grenoble, , France

Site Status

Countries

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France

Other Identifiers

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IRB 02021 - 097

Identifier Type: -

Identifier Source: org_study_id

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