Analysis of the Stress Induced by in Situ Simulation

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02494089

Acronym

SIMSTRESS

Enrollment

Registered

2015-07-10

Start date

2015-06-30

Completion date

2016-07-31

Last updated

2016-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Arrest, Psychologic Stress

Keywords

in situ simulation, in hospital cardiac arrest, clinical audit, education, patient simulation

Brief summary

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)).

Interventions

OTHERdistress analysis

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* team members: nurses, auxiliary nurse, residents, doctors, students

Exclusion criteria

* non volunteers

Design outcomes

Primary

Measure	Time frame	Description
psychologic distress analysis induced by in situ simulation	3 weeks	auto-validated distress inventory: IESR-R STAI-A STAI-B GHQ-12 JSS

Secondary

Measure	Time frame	Description
Stress vulnerability to in situ simulation	3 weeks	distress inventory: JSS STAI-A social questionary

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026