The Effect of Blended E-Learning Method on Students' Knowledge and Psychomotor Skills on Basic Life Support

August 2, 2022 updated by: Aynur KOYUNCU, Hasan Kalyoncu University

Investigation of the Effect of Blended E-Learning Method Given to Nursing Students on Students' Knowledge and Psychomotor Skills on Basic Life Support: A Pilot Study

The fact that Basic Life Support (BLS) training is factor determining survival necessitates the dissemination of BLS training. However, the fact that BLS training increases the workload of trainers and requires cost is one of the most important obstacles to the dissemination of this training. The search for new training methods with high efficiency and low cost continues in BLS training. Global guidelines recommend increasing quality of BLS and autonomous learning on BLS, and also encourage studies to develop methods related to this.

The use of e-training methods in BLS training is reported to be cost-effective as well as reducing the burden of trainers. In studies investigating the effectiveness of e-learning methods in BLS training, simulation models with feedback were used to evaluate psychomotor skills of the training. In this study, it was evaluated that it would be beneficial to apply a blended e-learning method, which includes video demonstrations of theoretical and BLS psychomotor skills, to nursing students in a virtual classroom environment. In evaluation of the psychomotor skills of BLS training, it was thought that a simple simulation model (Tshirt Dressed Simulation Pillow (TDSP)) could be created in home environment by wearing the tshirt with the sternum and heart print on a standard pillow (40 X 60 cm) in the student's home. It is thought that psychomotor skills will be improved with repetitive BLS applications that students will make on this model in the home environment. Two weeks after blended training, the BLS application will be made and evaluated on the real model. This training and assessment method is a new method that will allow the evaluation of BLS knowledge and the development of psychomotor skills with autonomous learning, and the fact that there is no study on this subject in the literature constitutes the original value of this study.

In this study, it is aimed to evaluate effects of the blended e-training method and TDSP model given to nursing students on the cognitive and psychomotor learning outcomes of the students on BLS.

The research is a randomized, controlled pilot study in a quasi-experimental design to be conducted at Hasan Kalyoncu University, Faculty of Health Sciences, Department of Nursing. The study was approved by Hasan Kalyoncu University Health Sciences Non-Interventional Research Ethics Committee. Written permission will be obtained. Before starting the study, the aims and objectives of the research will be explained to the students, information will be given about the blended e-learning method to be applied in the research, what the students should do within the scope of the research and data collection methods. Written and verbal consent will be obtained from the students who volunteered to participate in the study. The population of the research will be students (N=387) studying at Hasan Kalyoncu University, Faculty of Health Sciences, Department of Nursing in the 2021-2022 academic year. Students who have received BLS training for the first time, who have not practiced BLS before, and who voluntarily agree to participate in the study will be included in the study. The number of samples was determined as n=62 by power analysis. Students who accept to participate will be randomly divided into two groups through the computer program. The data collection tool consists of two forms, the form consisting of the introductory information of the students and the evaluation form of BLS knowledge and skills. The answers given to the cognitive questions and psychomotor skills of the nursing students in the study and control groups in the pre-test and post-test will be compared with appropriate statistical methods. A value of P<0.05 will be accepted for statistical significance.

Study Overview

Status

Recruiting

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

62

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 Contact

Study Locations

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

First time receiving BLS training, Those who have not applied BLS before, Students who accept to participate in the research voluntarily

Exclusion Criteria:

Students who have received BLS training or applied BLS before and who work as health professionals, The students who want to leave at any stage after participating in the research voluntarily

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention Group
In the pre-test, all students will be given a BLS information form, followed by blended e-learning with theory and video in a virtual environment. he BLS knowledge post-test will be administered immediately after class.T-shirts and standard pillows (550 g silicon fiber pillow 50x70 cm size) with a simulation of an adult human size (approximately) sternum, rib and heart drawing (printed as picture) will be given to the intervention group only after the pretest. In the study, the BLS will be simulated for adult patients only. To simulate a half-body human CPR mock-up, a pre-made simulation t-shirt will be fitted on a standard pillow to create a CPR mock-up in a home environment, and after blended e-learning, they will be able to perform CPR iteratively on a T-shirt-clad simulation pillow (TCSP) model. In this way, autonomous learning will be supported. All students will practice CPR in a real simulation model two weeks after the blended e-learning.
In the pre-test, all students will be given a BLS information form, followed by blended e-learning with theory and video in a virtual environment. The BLS knowledge post-test will be administered immediately after class.T-shirts and standard pillows (550 g silicon fiber pillow 50x70 cm size) with a simulation of an adult human size (approximately) sternum, rib and heart drawing (printed as picture) will be given to the intervention group only after the pretest. In the study, the BLS will be simulated for adult patients only. To simulate a half-body human BLS mock-up, a pre-made simulation t-shirt will be fitted on a standard pillow to create a BLS mock-up in a home environment, and after blended e-learning, they will be able to perform BLS iteratively on a T-shirt-clad simulation pillow (TCSP) model. In this way, autonomous learning will be supported. All students will practice BLS in a real simulation model two weeks after the blended e-learning.
No Intervention: Control Group
In the pretest, all students will be given a BLS knowledge test, followed by e-learning blended with theory and video in a virtual environment. The BLS knowledge post-test will be administered immediately after class. Two weeks after the blended e-learning, all students will practice CPR in a real simulation model. Psychomotor skills will be recorded in the evaluation form.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The effect of repeated applications with t-shirt dressed simulation pillow on psychomotor skills
Time Frame: Two weeks after the blended e-learning
The students in the study group will repeat the BLS application with the TDSP model given to them after the theoretical and video lessons, and the effect of frequent repetitions on psychomotor skills will be evaluated. The psychomotor skill evaluation form created by the researchers by using literature review will be used. For the content validity of this form, the opinions of five expert professionals who are experienced in their field were taken in accordance with the Davis technique.
Two weeks after the blended e-learning

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The effect of blended e-education on BLS knowledge level
Time Frame: Before the blended e-learning and immediately after the blended e-learning
It will be evaluated how theoretical and video BLS education affects the level of knowledge compared to classical education. For the evaluation of the information, the BLS Information Evaluation Form, which was created according to the literature review, will be used. For the content validity of this form, the opinions of five expert professionals who are experienced in their field were taken in accordance with the Davis technique.
Before the blended e-learning and immediately after the blended e-learning

Collaborators and Investigators

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

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)

May 28, 2022

Primary Completion (Anticipated)

August 28, 2022

Study Completion (Anticipated)

September 28, 2022

Study Registration Dates

First Submitted

April 4, 2022

First Submitted That Met QC Criteria

April 20, 2022

First Posted (Actual)

April 26, 2022

Study Record Updates

Last Update Posted (Actual)

August 3, 2022

Last Update Submitted That Met QC Criteria

August 2, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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