Retention and Retrieval for Three Different Training Methods

July 6, 2009 updated by: Doczero

Do we Need an Instructor, or a Manikin to Learn BLS/AED, or is Web Based Training as Good as Instructor Based Training?

The hypotheses that will be studied are:

H0: Providers trained by a web based application for skill competency in basic life support (BLS) and automated external defibrillation (AED) are as competent as those who were trained by certified instructors using the European Resuscitation Council (ERC) curriculum

H00-1: Providers who trained themselves with the used of web based training are more competent when they had a personal manikin for home exercise compared to providers who trained themselves with only a web based training

H0-2: Providers who did not receive any training will score lower than those who did.

Research questions for this study are:

  1. What are the results in skill competency for non trained people?
  2. What are the results in skill competency for trained people immediately after training?
  3. What is the retention of skills for trained and non trained people after six months?

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

280

Phase

  • Not Applicable

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

15 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • willing to follow a BLS/AED course

Exclusion Criteria:

  • CPR training within the last five years
  • professional health care provider

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
Active Comparator: Control-1
ERC-training by instructor
Standard way of training with an instructor
No Intervention: Control-2
No intervention
Experimental: Experimental-1
Web-based training only
Experimental way of training with a web based training application
Experimental: Experimental-2
Web-based training with a personal training manikin
Experimental way of training with a web based training application and a simple personal training manikin

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Kruskal-Wallis
Time Frame: 10-2007 - 03-2009
10-2007 - 03-2009

Collaborators and Investigators

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

Sponsor

Collaborators

Investigators

  • Principal Investigator: Wiebe de Vries, MSc, Doczero
  • Study Chair: Koenraad Monsieurs, Professor, University Hospital, Ghent
  • Study Director: Joost Bierens, Professor, VU Medical Centre
  • Study Chair: Rudolph Koster, PhD, Academical Medical Centre Amsterdam

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

October 1, 2007

Primary Completion (Anticipated)

March 1, 2009

Study Completion (Anticipated)

September 1, 2009

Study Registration Dates

First Submitted

July 2, 2009

First Submitted That Met QC Criteria

July 6, 2009

First Posted (Estimate)

July 7, 2009

Study Record Updates

Last Update Posted (Estimate)

July 7, 2009

Last Update Submitted That Met QC Criteria

July 6, 2009

Last Verified

July 1, 2009

More Information

Terms related to this study

Other Study ID Numbers

  • 081203_Ed-web

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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