Prospective Study of 3 Phone Assistance Strategies to Achieve a Continuous Cardiac Massage (TeleMacc)

June 18, 2014 updated by: University Hospital, Rouen

Prospective Study of 3 Phone Assistance Strategies to Achieve a Continuous Cardiac Massage During Training in Non-hospital Cardiac Cases.

This study must evaluate the benefit of a continuous audio guidance on the effectiveness of MCE directed by a volunteer.

The evaluation of the MCE for this study is based on both quantitative criteria (based on the recommendations ERC 2010)

  • frequency
  • depth of chest compressions.

This study compares two methods of continuous audio guide (one arm with an audio continuous guidance method by the regulator and second arm with an audio continuous guidance method by the controller relayed by an audio) to a method of incentive MCE based on a unique set made by the regulator(control arm).

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

210

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Rouen, France, 76031
        • CHU - Hôptaux de Rouen (Hôpital Charles Nicolle)

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

- Healthy volunteers from the general population understanding the French language.

Exclusion Criteria:

  • major physical disability;
  • do not speak French
  • first aid training under one year

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Single set (control Arm)
method of external cardiac massage incentive based on a single set. Intervention : Therapeutic and preventive strategies
Other: Therapeutic and preventive strategies
Single set (control Arm)
Other: Therapeutic and preventive strategies
Controller
Other: Therapeutic and preventive strategies
Audio
Experimental: Controller
Audio continuous guidance method by the controller. Intervention : Therapeutic and preventive strategies
Other: Therapeutic and preventive strategies
Single set (control Arm)
Other: Therapeutic and preventive strategies
Controller
Other: Therapeutic and preventive strategies
Audio
Experimental: Audio
Audio continuous guidance method by the controller relayed by an audio. Intervention : Therapeutic and preventive strategies
Other: Therapeutic and preventive strategies
Single set (control Arm)
Other: Therapeutic and preventive strategies
Controller
Other: Therapeutic and preventive strategies
Audio

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
frequency and depth of chest compressions
Time Frame: at the end of the simulation (10 minutes)
at the end of the simulation (10 minutes)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital, Rouen

Investigators

  • Principal Investigator: Cédric DAMM, Doctor, CHU - Hôpitaux de Rouen

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2013

Primary Completion (Actual)

September 1, 2013

Study Completion (Actual)

November 1, 2013

Study Registration Dates

First Submitted

September 2, 2013

First Submitted That Met QC Criteria

September 2, 2013

First Posted (Estimate)

September 6, 2013

Study Record Updates

Last Update Posted (Estimate)

June 19, 2014

Last Update Submitted That Met QC Criteria

June 18, 2014

Last Verified

June 1, 2014

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2012/182/HP
  • 2012-A01257-36 (Other Identifier: ID- RCB number)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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