NCT Number: NCT02494089
Analysis of the Stress Induced by in Situ Simulation
Vulnerability to psychologic distress induced by in situ simulation.
Objectives: Psychological evaluation at short and long term on working satisfaction, mental health, and acute stress after in situ simulation. Analysis of the stress vulnerability induced by simulation.
Design: non interventional study.
Primary outcome: Psychologic distress analysis with validated psychologic distress inventory (Job Satisfaction Survey (JSS), General Health Quality (GHQ), Impact of Event Scale Revisited (IESR), State-Trait Anxiety Inventory-A (STAI-A), State-Trait Anxiety Inventory -B (STAI-B)).
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- team members: nurses, auxiliary nurse, residents, doctors, students
Exclusion criteria
- non volunteers
Treatment and study plan
Primary outcomes
-
psychologic distress analysis induced by in situ simulation
Time frame: 3 weeks
auto-validated distress inventory: IESR-R STAI-A STAI-B GHQ-12 JSS
Secondary outcomes
-
Stress vulnerability to in situ simulation
Time frame: 3 weeks
distress inventory: JSS STAI-A social questionary
Sponsors and collaborators
Lead sponsor
Centre Hospitalier Universitaire de Besancon
Other
Registry information
Acronym: SIMSTRESS
Important dates
- Study start
- 2015
- Primary completion
- 2015
- Study completion
- 2016
- First posted
- Jul 10, 2015
- Registry last updated
- Jul 20, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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