SIMSTRESS: Analysis of the Stress Induced by in Situ Simulation

• Sponsor: Centre Hospitalier Universitaire de Besancon (Other)
• Overall Status: Completed
• CT.gov ID: NCT02494089
• Collaborator: (none)
• Enrollment: 53
• Duration (Months): 13

Study Details

Study Description

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)).

Condition or Disease	Intervention/Treatment	Phase
Psychologic Stress; Heart Arrest	Other: distress analysis

Study Design

• Study Type: Observational
• Actual Enrollment: 53 participants
• Observational Model: Case-Only
• Time Perspective: Prospective
• Official Title: Analysis of the Stress Induced by in Situ Simulation
• Study Start Date: Jun 1, 2015
• Actual Primary Completion Date: Sep 1, 2015
• Actual Study Completion Date: Jul 1, 2016

Outcome Measures

Primary Outcome Measures

1. psychologic distress analysis induced by in situ simulation [3 weeks]

   auto-validated distress inventory: IESR-R STAI-A STAI-B GHQ-12 JSS

Secondary Outcome Measures

1. Stress vulnerability to in situ simulation [3 weeks]

   distress inventory: JSS STAI-A social questionary

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

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

Exclusion Criteria:

• non volunteers

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

• Centre Hospitalier Universitaire de Besancon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Yannick BRUNIN, Doctor, Centre Hospitalier Universitaire de Besancon
• ClinicalTrials.gov Identifier: NCT02494089
• Other Study ID Numbers: SIM STRESS
• First Posted: Jul 10, 2015
• Last Update Posted: Jul 20, 2016
• Last Verified: Jul 1, 2016

• Keywords provided by Yannick BRUNIN, Doctor, Centre Hospitalier Universitaire de Besancon: in situ simulation; in hospital cardiac arrest; clinical audit; education; patient simulation
• Additional relevant MeSH terms: Heart Arrest; Stress, Psychological

Study Results

No Results Posted as of Jul 20, 2016