Virtual Reality Simulation for Nursing Education

October 17, 2023 updated by: Ayşe ARIKAN DÖNMEZ, Hacettepe University

Developing a Virtual Reality-Based Simulation Program for Nursing Students and Using in Nursing Research

Today, thanks to the developing hardware technology, various distance education projects are carried out with virtual reality, augmented reality and even mixed reality glasses. The visual writing fields of the content they provide can be extended as much as necessary.

With this research, it is aimed to develop a virtual reality-based simulation program and to ensure its use in nursing education and research.

Study Overview

Detailed Description

The universe of the research will consist of 219 students who are studying at Hacettepe University Faculty of Nursing in the Spring Semester of the 2021-2022 Academic Year and who have successfully completed the Internal Medicine Nursing course. As a result of the power analysis, it is aimed to reach a total of 100 people, with 50 students in each group. Our research was planned in a randomized controlled design. The data of the research will be collected through Student Information Form, Knowledge Tests, Perceived Learning Scale, General Self-Efficacy Scale, Satisfaction with Educational Methods Questionnaire and California Critical Thinking Disposition Scale. With this research, it is predicted that there will be an increase in nursing students' knowledge score, perceived learning, general self-efficacy, satisfaction with the education method, and critical thinking dispositions.

Study Type

Interventional

Enrollment (Actual)

100

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

      • Ankara, Turkey, 06100
        • Hacettepe University

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

Yes

Description

Inclusion Criteria:

  • Successfully completing the Internal Medicine Nursing Course
  • Having internet access
  • Volunteering to participate in the research

Exclusion Criteria:

  • Not being able to communicate in Turkish
  • Being in the intervention groups and not participating in the virtual simulation application
  • Not participating in any of the pre-test, post-test, or follow-up tests

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention Group
Nursing undergraduate students participating in a virtual reality simulation program
Virtual reality applications are a type of three-dimensional computer-based simulation that gives a sense of being anywhere and provides various data to the sense organs for this. However, virtual reality applications are a simulation model that creates a sense of reality for the participants and allows mutual communication with a computer-based dynamic environment.
No Intervention: Control Group
Nursing undergraduate students receiving attention-matched training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge Tests
Time Frame: Changes from baseline to one day post-test and after one month follow-up
In order to determine the cognitive learning of the students, questionnaires consisting of 20 multiple-choice questions for each subject and to be evaluated over 100 points will be created. A literature review will be made for the creation of questionnaires and these forms will be created to determine cognitive competencies in line with the educational content. Validity and reliability studies will be conducted to test the usability of the forms.
Changes from baseline to one day post-test and after one month follow-up
Perceived Learning Scale
Time Frame: Changes from baseline to one day post-test and after one month follow-up
Perceived Learning Scale Rovai et al. (2009) developed by. The validity and reliability studies of the scale were performed by Albayrak et al. (2004) with 227 university students. The scale has 9 items and three factors, and the first factor is "Cognitive", which includes three items aiming to measure cognitively perceived learning. The second factor was named "Affective", which includes three items aiming to measure learning perceived as affective, and the third factor, "Psychomotor", which aims to measure learning perceived as psychomotor. A score between 9 and 63 is obtained from the entire scale. An increase in the scale score indicates an increase in the perceived learning level. The Cronbach's alpha, which includes all nine items of the scale for internal consistency, was .83.
Changes from baseline to one day post-test and after one month follow-up
Satisfaction Survey with Training Methods
Time Frame: Changes from baseline to one day post-test and after one month follow-up
Training methods satisfaction questionnaire was developed by Gürpınar (Cronbach alpha: 0.84) and used in his studies. The questionnaire consists of 16 propositions. One of these propositions is the proposition "I am satisfied with this education method in general", which questions the state of being satisfied with the education. Other propositions were formed from propositions aiming to determine the views of the education method in general about the contribution of the education method to the learning and professional life of the student. It is determined that as the scale score average increases, the satisfaction of the students in the education method increases, and as the scale score average decreases, their satisfaction in the education method decreases. In the evaluation of the scale, students are given a minimum of 16 and a maximum of 80 points for their satisfaction with education methods. Atan et al. (2019), the Cronbach alpha value of the scale was found to be 0.90.
Changes from baseline to one day post-test and after one month follow-up
Critical Thinking Disposition Scale
Time Frame: Changes from baseline to one day post-test and after one month follow-up
This scale was developed by Facione in 1990, and its validity and reliability study in Turkey was carried out by Kökdemir in 2003. It consists of 51 items and six subscales. The scale is a six-item Likert-type scale. The score range of the scale is 51-306. A low score indicates a low critical thinking disposition, and a high score indicates a high critical thinking disposition. The Cronbach's alpha value of the scale was found to be 0.88.
Changes from baseline to one day post-test and after one month follow-up
General Self-Efficacy Scale
Time Frame: Changes from baseline to one day post-test and after one month follow-up
The Turkish validity and reliability study of the General Self-Efficacy scale, which was developed by Schwarzer and Jarusalem in Germany in 1981, was performed by Aypay (2010). The scale, which is all positive and consists of 10 items, was prepared in a 4-point Likert type limited to completely wrong and completely true points. All items are positively scored and a score between 10 and 40 is obtained. A high score means high general self-efficacy. The cronbach's alpha coefficient of the scale was found to be 0.83.
Changes from baseline to one day post-test and after one month follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 23, 2023

Primary Completion (Actual)

May 31, 2023

Study Completion (Actual)

May 31, 2023

Study Registration Dates

First Submitted

April 13, 2022

First Submitted That Met QC Criteria

June 17, 2022

First Posted (Actual)

June 23, 2022

Study Record Updates

Last Update Posted (Actual)

October 19, 2023

Last Update Submitted That Met QC Criteria

October 17, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • KA-21126

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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