- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05248542
The Effects of Virtual Reality/ Augmented Reality Usage on Oral Care Knowledge in Nursing Students
February 9, 2022 updated by: Kaohsiung Medical University Chung-Ho Memorial Hospital
The aim of this study was to investigate the effects of virtual reality usage on oral care knowledge in nursing students.
The participants were randomly assigned to virtual-reality experimental and control groups.
The students in experimental group received a 30 minutes virtual reality (VR) training for elderly oral health care at the second week and the fourth week after the first time survey.
All students self-administrated questionnaire three times at first date of consent form signed, immediately after each of the intervention for period of two weeks.
Linear regression in generalized estimating equations (GEE) compare the differences between both groups.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
A total of 50 first-year to third-year undergraduate nursing students were included from the Department of Nursing, Kaohsiung Medical University, Taiwan.
The students were randomly assigned divided at random into two groups, control (n = 25) and experimental (n = 25).
Study Type
Interventional
Enrollment (Actual)
50
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
-
-
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Kaohsiung, Taiwan
- Kaohsiung Medical University
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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
18 years to 25 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- undergraduate freshman, sophomore, and junior nursing students
- those volunteered to participate in this study
Exclusion Criteria:
- students with known negative effects of using VR devices, such as nausea, vomiting, etc.
- those under 20 years of age who had not obtained the consent of a legal representative to participate in this study.
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Virtual Reality group
Each participant in the experimental group received a 30 minutes of individualized VR-based simulation education in a dedicated oral skills training room.
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Virtual Reality Usage on Oral Care Knowledge about independent older adults
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No Intervention: Control group
The control group only received repeated questionnaires and did not receive any education about geriatric oral hygiene.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge of geriatric oral hygiene scale
Time Frame: through study completion, an average of 4 weeks
|
There were 10 items to evaluate the participants' knowledge of the geriatric oral hygiene scale Each item had three response options: true, false, and unknown.
The total score ranged from 0 to 10 and a higher score indicated a higher level of knowledge of geriatric oral hygiene.
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through study completion, an average of 4 weeks
|
|
Attitudes of geriatric oral hygiene scale
Time Frame: through study completion, an average of 4 weeks
|
The attitudes of geriatric oral hygiene scale included seven items.
Each item was scored on a five-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree).
The total score ranged from 5 to 35 and a higher score indicated a positive attitude toward geriatric oral hygiene.
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through study completion, an average of 4 weeks
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Self-efficacy of geriatric oral hygiene scale
Time Frame: through study completion, an average of 4 weeks
|
The self-efficacy of geriatric oral hygiene scale included ten items.
Each item was scored on a five-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree) and the higher score was for a higher level of self-efficacy of geriatric oral hygiene, vise versa.
The total score ranged from 5 to 50.
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through study completion, an average of 4 weeks
|
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Behavioral intention of geriatric oral hygiene scale
Time Frame: through study completion, an average of 4 weeks
|
The behavioral intention scale of the geriatric oral hygiene included ten items.
Each item was scored on a five-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree), with a higher score indicated a higher level of the behavioral intention of geriatric oral hygiene.
The total score ranged from 5 to 50.
|
through study completion, an average of 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Pei-Chao Lin, Kaohsiung Medical University
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, 2021
Primary Completion (Actual)
April 19, 2021
Study Completion (Actual)
November 12, 2021
Study Registration Dates
First Submitted
December 30, 2021
First Submitted That Met QC Criteria
February 9, 2022
First Posted (Actual)
February 21, 2022
Study Record Updates
Last Update Posted (Actual)
February 21, 2022
Last Update Submitted That Met QC Criteria
February 9, 2022
Last Verified
December 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- KMUHIRB-SV(II)-20200062
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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