NCT02065934

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
22

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Dec 2013

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2013

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

January 13, 2014

Completed
1 month until next milestone

First Posted

Study publicly available on registry

February 19, 2014

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2015

Completed
Last Updated

July 8, 2015

Status Verified

July 1, 2015

Enrollment Period

1.5 years

First QC Date

January 13, 2014

Last Update Submit

July 7, 2015

Conditions

in Hospital Cardiac Arrestin Situ SimulationClinical AuditEducation

Keywords

in hospital cardiac arrestin situ simulationclinical auditeducation

Outcome Measures

Primary Outcomes (1)

  • In-Hospital resuscitation scale

    5 months

Secondary Outcomes (3)

  • ANTS scale

    5 months

  • Peritraumatic Dissociative Experiences Questionnaire (PDEQ)

    5 months

  • Peritraumatic Distress Inventory (PDI)

    5 months

Interventions

cardio-pulmonary resuscitationOTHER

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Team members

You may qualify if:

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

You may not qualify if:

  • non volunteers

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Besancon

Besançon, Doubs, 25000, France

Location

MeSH Terms

Interventions

Cardiopulmonary Resuscitation

Intervention Hierarchy (Ancestors)

ResuscitationEmergency TreatmentTherapeutics

Study Officials

  • Yannick BRUNIN, Dr

    Centre Hospitalier Universitaire de Besancon

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD

Study Record Dates

First Submitted

January 13, 2014

First Posted

February 19, 2014

Study Start

December 1, 2013

Primary Completion

June 1, 2015

Study Completion

June 1, 2015

Last Updated

July 8, 2015

Record last verified: 2015-07

Locations

FR(1)