Study Results
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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COMPLETED
34 participants
OBSERVATIONAL
2021-06-18
2021-11-15
Brief Summary
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Detailed Description
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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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Study Design
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OTHER
PROSPECTIVE
Interventions
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SDNN measurement
SDNN measurement during pediatric simulation
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* 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
18 Years
ALL
Yes
Sponsors
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University Hospital, Grenoble
OTHER
Responsible Party
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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
Countries
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Other Identifiers
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IRB 02021 - 097
Identifier Type: -
Identifier Source: org_study_id
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