- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07535216
VR Learning Program for Sexual-and-gender-diversity Care
April 14, 2026 updated by: Sheng-Miauh Huang, National Yang Ming Chiao Tung University Hospital
Using Temporal Self-regulation Theory to Create a VR Learning Program for Sexual-and-gender-diversity Care and Evaluating the Effect on Caring Behaviors in Nursing Students: A Series of Studies
The study is designed to create a VR learning program for sexual-and-gender-diversity care and compare the short-term and long-term effects on caring behaviors in nursing students.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
130
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
-
-
-
Taipei, Taiwan
- National Yang Ming Chiao Tung 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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- At least 80 hours of nursing practice experience
Exclusion Criteria:
- Visual impairment
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: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Control group
The control group will receive the traditional SGD care learning program.
|
The experimental group will receive SGD care VR learning program via the teaching web platform as the intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Caring Behaviors Scale
Time Frame: Six month
|
The Caring Behaviors Scale (CBS) with Chinese version, with 27 items, was used to measure students' caring behaviors.
The three domains of the scale are patient advocacy, knowing the patient, and helping the patient through the illness trajectory.
The CBS is a four-point Likert scale to measure the frequency of caring behavior.
The range of total scores was between 0 and 81.
Higher scores indicate a greater frequency of caring behaviors.
|
Six month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Jefferson Scale of Empathy
Time Frame: Six month
|
Empathy was measured using the Chinese version of the Jefferson Scale of Empathy- Healthcare Providers (JSE-HP), developed based on a literature review.
The components of the scale included perspective-taking, compassionate care, and standing in the patient's shoes.
The JSE-HP is a 7-point Likert scale, with a score of 1 indicating strong disagreement and 7 indicating strong agreement.
Ten of the 20 questions were negative, and 10 were positive, with a total score of 20-140, with higher scores indicating more positive empathy.
|
Six month
|
|
Nursing Student Competence Scale
Time Frame: Six month
|
The Nursing Student Competence Scale (NSCS) with Chinese version was used to measure students' nursing competence.
The NSCS with 30 items includes six dimensions: medical-related knowledge (5 itesm), basic nursing skills (5 itesm), communication and cooperation (5 itesm), lifelong learning (5 itesm), global vision (5 itesm), and critical thinking (5 itesm).
The responses to each item were based on a 5-point Likert scale, with a score of 1 indicating strong disagreement and 5 indicating strong agreement.
A higher scale score meant a greater nursing ability.
The range of total scores was between 5 and 150.
|
Six month
|
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.
Helpful Links
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)
August 1, 2025
Primary Completion (Estimated)
July 31, 2027
Study Completion (Estimated)
July 31, 2027
Study Registration Dates
First Submitted
April 8, 2026
First Submitted That Met QC Criteria
April 14, 2026
First Posted (Actual)
April 17, 2026
Study Record Updates
Last Update Posted (Actual)
April 17, 2026
Last Update Submitted That Met QC Criteria
April 14, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- NSTC 114-2410-H-A49-086
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.
Clinical Trials on Sex Difference
-
Medizinische Hochschule Brandenburg Theodor FontaneMargarete-Ammon-StiftungCompletedSex Difference | Gastric (Stomach) Cancer
-
Yale-NUS CollegeCompleted
-
Beijing Friendship HospitalUnknownPostoperative Pain | Preemptive Analgesia | Sex Difference | Flurbiprofen Axetil | Postoperative Sleep Quality
-
Yale-NUS CollegeCompletedIndividual DifferenceSingapore
-
Chulalongkorn UniversityRatchadapiseksompotch Research FundCompleted
-
Virginia BRANCOUnknownIndividual Difference | Environmental Exposure
-
Assistance Publique Hopitaux De MarseilleRecruitingDifference in Regional Brain ActivityFrance
-
Tel-Aviv Sourasky Medical CenterUnknownDifference in BMD Between Both Hips
-
Erasme University HospitalTerminatedDifference, IndividualBelgium
-
Hospital for Special Surgery, New YorkCompletedDifference Between Femoral Nerve Block and Saphenous BlockUnited States
Clinical Trials on VR learning program for SGD care
-
First Affiliated Hospital of Shantou University...TerminatedAnterior Cruciate Ligament (ACL) Reconstruction | Preoperative RehabilitationChina
-
Taipei Medical UniversityCompletedChemotherapy TrainingTaiwan
-
University of Illinois at ChicagoActive, not recruitingBurnout, Professional | Stress, Psychological | Anxiety | Prosocial Behavior | Efficacy, Self | Self-Compassion | Optimism | Social Competence | Self Awareness | Community SenseUnited States
-
National Taipei University of Nursing and Health...Completed
-
Chang Gung University of Science and TechnologyNot yet recruitingHealth Education | Aged | Experiential LearningTaiwan
-
The Hong Kong Polytechnic UniversityRecruitingSmoking CessationHong Kong
-
Education University of Hong KongTung Wah College; Guangzhou University of Chinese Medicine; Xinhua Hospital,... and other collaboratorsCompleted
-
Klein Buendel, Inc.National Institute on Aging (NIA); Penn State UniversityCompleted
-
NYU Langone HealthCompleted
-
Eye & ENT Hospital of Fudan UniversityThe Affiliated Eye Hospital of Nanjing Medical University; Suqian First People...Completed