Bystander Helping Behaviour for Myocardial Infarction Following First Aid Training

May 2, 2011 updated by: KU Leuven

Bystander Helping Behaviour for Acute Myocardial Infarction Following a First Aid Training Programme That Draws Attention to the Barriers to Providing Help - Protocol for a Randomized Controlled Trial

The objective of this study is to measure the effect of an innovative training programme on the help seeking behaviour and helping rates of bystanders in medical emergencies.

Study Overview

Detailed Description

A systematic review on the effects of first aid training concluded that training must also include ways to overcome obstacles to bystander intervention. This could lead to better help and higher helping rates in medical emergencies.

The objective of this paper is to measure the effect of an innovative training programme on the help seeking behaviour and helping rates of bystanders in medical emergencies. We chose to test the helping behaviour for acute myocardial infarction because it is an important cause of mortality and invalidity. While the victim is urgently in need of help, delay in seeking professional help is an important problem.

Study Type

Interventional

Enrollment (Actual)

144

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

      • Mechelen, Belgium, 2800
        • Belgian Red Cross-Flanders

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Course participants that are 18 years or older

Exclusion Criteria:

  • Course participants that are younger than 18 years
  • Health care students
  • Health care professionals

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

  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: first aid and helping behaviour
The helping behaviour training is given after 24 hours first aid training and aims to sensitise participants towards a helping reaction and teach participants how to deal with barriers to helping
The objective of the helping behaviour curriculum is to sensitise participants to develop a helping reaction, and to teach participants how to deal with barriers to helping. The helping behaviour curriculum is being taught in 2hours.
Active Comparator: first aid only
This group receives training in first aid only without training in helping behaviour.
Two hours training on first aid for alcohol and drug incidents

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Delay time for seeking help during deception experiment
Time Frame: within 4 weeks after the control or intervention training
Time to seeking help was measured between the simulated patient grabbing the heart and the study participant opening the door to get help.
within 4 weeks after the control or intervention training

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rate of helping during deception experiment
Time Frame: within 4 weeks after control or intervention training
This refers to the number of participants that assessed the victim, or asked for help, or provided direct help to the victim during the test.
within 4 weeks after control or intervention training
First aid self efficacy belief
Time Frame: within 15 minutes after experimental or control intervention
scores on 6 questions related to helping behaviour barriers with the following structure: " I will do x (action) even if y (barrier)"
within 15 minutes after experimental or control intervention
Impact of event
Time Frame: Within 15 minutes after deception experiment
This indicates how shocking the study participants found the simulated emergency situation
Within 15 minutes after deception experiment
State of mood
Time Frame: Within 15 minutes after deception experiment
Indication of how study participants feel after being told about the deception.
Within 15 minutes after deception experiment
Credibility of deception
Time Frame: Within 15 minutes after deception
Indication of how credible study participants found the simulated emergency situation
Within 15 minutes after deception

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Bert Aertgeerts, Academic Centre for General Practice, Catholic University Leuven

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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, 2009

Primary Completion (Actual)

January 1, 2011

Study Completion (Actual)

January 1, 2011

Study Registration Dates

First Submitted

August 6, 2009

First Submitted That Met QC Criteria

August 6, 2009

First Posted (Estimate)

August 7, 2009

Study Record Updates

Last Update Posted (Estimate)

May 3, 2011

Last Update Submitted That Met QC Criteria

May 2, 2011

Last Verified

May 1, 2011

More Information

Terms related to this study

Other Study ID Numbers

  • S51742
  • S51742, ML5859, B32220096701 (Other Identifier: Commissie Medische Ethiek UZ Gasthuisberg)

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.

Subscribe