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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05248542
Other study ID # KMUHIRB-SV(II)-20200062
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 23, 2021
Est. completion date November 12, 2021

Study information

Verified date December 2021
Source Kaohsiung Medical University Chung-Ho Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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).


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date November 12, 2021
Est. primary completion date April 19, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: 1. undergraduate freshman, sophomore, and junior nursing students 2. those volunteered to participate in this study Exclusion Criteria: 1. students with known negative effects of using VR devices, such as nausea, vomiting, etc. 2. those under 20 years of age who had not obtained the consent of a legal representative to participate in this study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Virtual Reality Usage on Oral Care Knowledge
Virtual Reality Usage on Oral Care Knowledge about independent older adults

Locations

Country Name City State
Taiwan Kaohsiung Medical University Kaohsiung

Sponsors (1)

Lead Sponsor Collaborator
Kaohsiung Medical University Chung-Ho Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Knowledge of geriatric oral hygiene scale 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. through study completion, an average of 4 weeks
Primary Attitudes of geriatric oral hygiene scale 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. through study completion, an average of 4 weeks
Primary Self-efficacy of geriatric oral hygiene scale 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. through study completion, an average of 4 weeks
Primary Behavioral intention of geriatric oral hygiene scale 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
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