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OpenTrials
Completed

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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Key information

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

distress analysis

Other

Primary outcomes

  1. 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

  1. 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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