An observational study in Psychologic Stress and Heart Arrest, sponsored by Centre Hospitalier Universitaire de Besancon. Completed. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-07-20.
Sponsored by Centre Hospitalier Universitaire de Besancon · Observational
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)).
965 studies on the registry are indexed under Heart Arrest; 226 are open to participants now.
This study's enrollment of 53 is below the median of 200 across 382 observational studies indexed under Heart Arrest.
Browse Heart Arrest studies →Centre Hospitalier Universitaire de Besancon is the lead sponsor of 439 studies on the registry; 97 are open to participants now.
Counted across the registry records on this site, refreshed daily.
team members
Exclusion Criteria:
psychologic distress analysis induced by in situ simulation
auto-validated distress inventory: IESR-R STAI-A STAI-B GHQ-12 JSS
Time frame: 3 weeks
Stress vulnerability to in situ simulation
distress inventory: JSS STAI-A social questionary
Time frame: 3 weeks
No study locations are listed for this record.
This study is completed, as verified in Jul 2016. You cannot join it, but the record below documents what was studied.
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Centre Hospitalier Universitaire de Besancon