- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05428904
Virtual Reality Simulation for Nursing Education
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
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Ankara, Turkey, 06100
- Hacettepe University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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
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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.
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No Intervention: Control Group
Nursing undergraduate students receiving attention-matched training
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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.
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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.
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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.
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Changes from baseline to one day post-test and after one month follow-up
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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.
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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.
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Changes from baseline to one day post-test and after one month follow-up
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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