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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02065934
Other study ID # EI/2013/116
Secondary ID
Status Completed
Phase N/A
First received January 13, 2014
Last updated July 7, 2015
Start date December 2013
Est. completion date June 2015

Study information

Verified date July 2015
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority France : Ministère de l'Enseignement et de la Recherche
Study type Observational

Clinical Trial Summary

Clinical audit of in-hospital cardiac arrest management by in situ simulation

Objectives: correct latent safety threats, knowledge gap, and crisis resource management (CRM)

Design: clinical audit, observational sudy. Primary outcome: In Hospital resuscitation scale. Exploratory outcomes: non technical skills, validated stress inventory, and questionnaire on perceptions of the simulation and organisational changes needed.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- team members: nurses, auxiliary nurses, residents, doctors, students

Exclusion Criteria:

- non volunteers

Study Design

Time Perspective: Prospective


Intervention

Other:
cardio-pulmonary resuscitation


Locations

Country Name City State
France CHU Besancon Besancon Doubs

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary In-Hospital resuscitation scale 5 months No
Secondary ANTS scale 5 months No
Secondary Peritraumatic Dissociative Experiences Questionnaire (PDEQ) validated stress inventory 5 months No
Secondary Peritraumatic Distress Inventory (PDI) validated stress inventory 5 months No
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