Pedagogical Aspects on Training in Basic Life Support

March 26, 2020 updated by: Helene Bylow, University of Boras

Pedagogical Aspects on Education in Basic Life Support: A Cluster Randomized Trial on Effectiveness, Comparing Different Educational Methods for Adults in the Society of Sweden.

Cardio vascular disease (CVD) including out-of-hospital cardiac arrest (OHCA) is still the leading cause of death in a global perspective. Start of cardiopulmonary resuscitation (CPR) with automated external defibrillator (AED) may double or quadruple survival. Scientific research on education in Basic Life Support (BLS) in the society is active in different part of Europe but low in Sweden. The aim of this study is to investigate the effectiveness and retention after different training interventions in BLS and willingness to act in a real-life cardiac arrest situation in the society of Sweden, based on European Resuscitation Council (ERC) guidelines. This is an experimental cluster randomized trial, including participants from a BLS education project in Sweden.

Study Overview

Detailed Description

Introduction: The single most important factor for survival from sudden cardiac arrest (SCA) is to minimize the time from cardiac arrest to cardiopulmonary resuscitation (CPR) and to provide an electric chock through the heart with an automated external defibrillator (AED). Early start with CPR-AED increases the chance of survival two to four times. It is therefore important that as many people as possible have knowledge to quickly identify SCA and to start CPR-AED.

In this research, education efforts are directed for the adult public at workplaces in Sweden. The Investigator have designed an intervention in accordance to guidelines from European Resuscitation Council (ERC) and the Swedish national education for Basic Life Support (BLS).

This is a cluster randomized trial primarily comparing in the first study, instructor-led training as the control group and self-learning training as the experimental group. In the second study the Investigator plan to compare a preparatory web-education on CVD before the BLS training versus no web-education before the BLS. The Investigator have conducted quality tests on practical skills on BLS, administered questionnaires to the participants about theoretical knowledge, self-assessed confidence and willingness to act in a real-life SCA situation. It is crucial to be able to identify factors that affect knowledge and retention after BLS training and the willingness to intervene in an acute situation.

Background: With modern IT technology, several different options and learning strategies are available. At the same time pedagogical thoughts have emerged on learning. Education can be instructor-led or self-directed and with preparatory courses for theoretical knowledge. The quality of BLS skills and theoretical knowledge can be measured through validated instruments. Against this background, the research goal is to identify how the study can improve retention and which training methods for BLS that should be recommended for the public in the future.

Objectives: The overall objective is to increase survival from OHCA. The aim is to identify factors that affect retention and contributes to intended practical skills, theoretical knowledge and willingness to act after BLS training and whether these goals are affected by the type of training intervention.

Hypothesis: The main hypothesis is that retention of practical skills after BLS training is affected by the type of educational intervention. The hypothesis in the first study is that an instructor present at the time of training have a positive impact on retention six months after the intervention compared to self-directed training. In the second study the hypothesis is that a preparatory web-education on CVD before the BLS has a positive impact on retention six months after intervention compared to no web-education.

Questions: The Primary question is which intervention is most effective for the total score and contributes to intended practical skills and adherence to protocol, the BLS algorithm, six months after the intervention. Secondary questions deal with if other variables such as practical skills, theoretical knowledge, self-assessed confidence and willingness to intervene in a SCA situation are affected when comparing each intervention both direct after and six months after training.

Method: Voluntary, participants from a BLS project at workplaces in Sweden have been included. The participants have been randomized from a randomization list and organized for the study, from an independent coordinator. After training and at six months, a quantitative approach and data collection measured the quality of practical skills in a simulated SCA scenario, on a Laerdal Resusci Anne manikin, connected to the PCSkillReporting system. The assessor was blinded for the type of training intervention. At data collection, the variables were structured according to a modified international quality test, Cardiff Test of basic life support and automated external defibrillation (Cardiff Test) that scored adherence to the treatment algorithm and practical skills. The modified Cardiff Test included 19 variables with a total score of 70 points. A questionnaire scored theoretical knowledge, self-assessed confidence and willingness to act in a real-life situation. At the practical quality tests, the total score was the primary endpoint with other individual variables as the secondary endpoint.

Study population: Strategic sampling was used to include participants from different workplaces in a number of counties in Sweden.

Planned Studies: 1) Self-learning training versus Instructor-led training. 2) A preparatory web-education on CVD before the BLS training versus no web-education before the BLS training. 3) A register study on bystander activity 4) Instructor-led training versus subgroups of training from the BLS intervention project.

Statistics: All statistical analyses will be analysed in SASforwindows and calculated on a cluster level with an alpha level of five percent.

Ethical considerations: Ethical principles for research are carefully considered in the research process. Ethical vetting from Ethical Review of Research, involving Humans is approved (Regional Ethical Review Board in Gothenburg, diaries number 134-14) and Guidelines from the Swedish Research Council, Good Research Practice is actively used. Information has been given both individually to all participants and to the working places. All participant had to read and sign a personal consent form before participating. The result will be published according to the Declaration of Helsinki.

Study Type

Interventional

Enrollment (Actual)

2623

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

      • Borås, Sweden, SE 501 90
        • University of Borås Sweden

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

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion criteria

  • Adults in society over eighteen years old
  • Working at workplaces outside hospital
  • Without training in BLS or within the past five years
  • A completed and signed consent form.

Exclusion criteria

  • Participants younger than 18 years old
  • Undergone training on BLS within the past five years
  • Working at hospital as health care personnel
  • Do not want to participate

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Instructor-led training
Instructor-led training contents a supervised practical training for BLS, facilitated by a certified instructor.
The Instructor-led training contents a supervised practical training with a standard kit for training in BLS
Experimental: Self-learning training
Self-learning training is self-directed and contents practical training for BLS
The self-learning training contents a standard kit for self-directed training in BLS

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total score from Cardiff Test for retention at 6 months
Time Frame: 6 months after intervention
Total score from the modified instrument Cardiff Test on the participants individual practical skills and adherence to the Basic Life Support algorithm in retention-test at six months after intervention.
6 months after intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Individual quality variables from PC SkillReporting System at baseline and at retention at 6 months.
Time Frame: 0 days + 6 months later
Individual quality variables from the instrument and data program PC SkillReporting system on the participants quality on practical skills for Basic Life Support at baseline as post-test direct after intervention, as retention-test at six months later and as a change in quality of Basic Life Support
0 days + 6 months later
Self-assessed theoretical knowledge from questionnaires at baseline and retention at 6 months
Time Frame: 0 days + 6 months later
Self-assessed theoretical knowledge with data collected from the participants individual questionnaires at baseline as post-test direct after intervention and as retention-test at six months later.
0 days + 6 months later
Self-assessed confidence from questionnaires at baseline and retention at 6 months
Time Frame: 0 days + 6 months later
Self-assessed confidence after the intervention with data collected from the participants individual questionnaires at baseline and retention at six months later.
0 days + 6 months later
Self-assessed willingness from questionnaires at baseline and retention at 6 months
Time Frame: 0 days + 6 months later
Self-assessed willingness to act in a real-life sudden cardiac arrest situation with data collected from the participants individual questionnaires at baseline and retention at six months later.
0 days + 6 months later
Theoretical knowledge on cardio vascular disease, symptoms and first actions from questionnaires at baseline and retention at 6 months
Time Frame: 0 days + 6 months later
Theoretical knowledge on cardio vascular disease, first actions and healthy life style factors with data collected from the participants individual questionnaires at baseline and retention at six months later. Secondary Outcome for study 2) A preparatory web-education on CVD before the BLS training versus no web-education before the BLS training.
0 days + 6 months later
Self-assessed experience on learning outcome at baseline and retention at 6 months
Time Frame: 0 days + 6 months later
Self-assessed experience on the participants individual learning outcome at baseline and retention at six months with data collected from the participants individual questionnaires at baseline and retention at six months later. Secondary Outcome for study 4) Instructor-led training versus subgroups of training from the BLS intervention project.
0 days + 6 months later

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Johan D Herlitz, Professor, University of Borås Sweden

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 (Actual)

March 1, 2014

Primary Completion (Actual)

December 31, 2016

Study Completion (Actual)

December 31, 2019

Study Registration Dates

First Submitted

July 21, 2018

First Submitted That Met QC Criteria

August 5, 2018

First Posted (Actual)

August 7, 2018

Study Record Updates

Last Update Posted (Actual)

March 27, 2020

Last Update Submitted That Met QC Criteria

March 26, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

Data will be analysed and published on group level only

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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