NCT01992419

Brief Summary

The purpose of this study is to measure an improvement in the detection rate of cardiac arrest (CA) in the Dispatch Center as a result of debriefings and repeated trainings for non-medical operators who receive emergency calls.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2013

Shorter than P25 for all trials

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

November 1, 2013

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

November 7, 2013

Completed
18 days until next milestone

First Posted

Study publicly available on registry

November 25, 2013

Completed
6 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2013

Completed
Last Updated

December 9, 2013

Status Verified

December 1, 2013

Enrollment Period

1 month

First QC Date

November 7, 2013

Last Update Submit

December 6, 2013

Conditions

Keywords

Out-of-hospital Cardiac arresttelephone dispatch assisted resuscitationcardiac arrest phone detection

Outcome Measures

Primary Outcomes (1)

  • Ratio of CA Detected by the emergency dispatcher

    one year

Secondary Outcomes (1)

  • o Median time between the start of the emergency call and the pronunciation of the words "chest compressions," by the dispatcher

    one year

Other Outcomes (2)

  • Median time elapsed between the start of the emergency call and the actual start of chest compressions by caller

    one year

  • Evaluation of the ventilation mode (hand on abdomen YES/NO, count the interval between two ventilatory movements YES/NO)

    one year

Eligibility Criteria

Age15 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

residents of Paris urban and suburban area

You may qualify if:

  • Patient over 15 years old (adult morphology) suffering Out-of-hospital Cardiac Arrest before or during the call to the Dispatch Center
  • Patient who benefited from the installation of a automated external defibrillator (AED) before or at the time of arrival of the rescuers on the scene

You may not qualify if:

  • Patient conscious at the time of the call
  • OHCA between the end of the phone call and the arrival of rescuers on site
  • OHCA after the rescuers' arrival on site
  • Dispatch Center alerted on "second line" from another institution (Police, SAMU), without the possibility of joining the first caller.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Paris Fire Brigade Emergency Dept

Paris, France, 75017, France

Location

MeSH Terms

Conditions

Out-of-Hospital Cardiac Arrest

Condition Hierarchy (Ancestors)

Heart ArrestHeart DiseasesCardiovascular Diseases

Study Officials

  • Jean-Pierre TOURTIER, MDPhD Prof

    Paris Fire Brigade - Emergency Medical Dept

    STUDY CHAIR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Target Duration
1 Year
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Doctor, responsible for clinical research at Paris Fire Brigade

Study Record Dates

First Submitted

November 7, 2013

First Posted

November 25, 2013

Study Start

November 1, 2013

Primary Completion

December 1, 2013

Study Completion

December 1, 2013

Last Updated

December 9, 2013

Record last verified: 2013-12

Locations