- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06605781
Enhancing Psychiatric Nursing Skills in Auditory Hallucination Assessment Via AR/VR and Virtual OSCE
Enhancing Auditory Hallucination Assessment and Intervention Skills of Psychiatric Nursing Student Through AR/VR Technology and OSCE in Virtual Clinical Environments
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study employs a quasi-experimental design and uses a convenience sampling method to select senior students from a university nursing program as participants. The study aims to recruit 150 nursing students. The research involves two institutions, with participants being divided into groups within each institution. The students will be randomly assigned by computer into two groups: an experimental group and a control group. The experimental group will receive AR/VR technology-based group training within a virtual clinical environment during their practicum, while the control group will watch educational videos and participate in a general discussion group focused on auditory hallucinations.
Data will be collected using Google Forms at two time points: baseline and post-intervention. The research instruments include:
- A self-assessment questionnaire on confidence in auditory hallucination assessment and intervention;
- A scale measuring nursing students' knowledge, attitudes, and perceived empathy toward auditory hallucinations;
- The Auditory Hallucination Situational Involvement and Empathy Scale;
- An OSCE (Objective Structured Clinical Examination) evaluation form that assesses auditory hallucination assessment skills, empathy toward auditory hallucinations, communication skills, and the ability to manage auditory hallucinations." Data will be analyzed using IBM SPSS 24.0 for descriptive statistics and for comparing outcomes between the experimental group and the control group.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Chiu Yueh Yang, PhD
- Phone Number: +8862-2826-7388
- Email: cyyang3@ym.edu.tw
Study Contact Backup
- Name: Mu Hsi Young, MS
- Phone Number: +886972-102-204
- Email: deborahyounglulu33@gmail.com
Study Locations
-
-
Taipei City
-
Taipei, Taipei City, Taiwan, 112304
- National Yang Ming Chiao Tung University
-
Contact:
- Chiu Yueh Yang, PhD
- Phone Number: +8862-2826-7388
- Email: cyyang3@ym.edu.tw
-
Contact:
- Mu Hsi Young, MS
- Phone Number: +886972-102-204
- Email: deborahyounglulu33@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Nursing students who are about to undertake their psychiatry practicum.
- Those who are willing to join the study and sign the consent form.
- Those who are willing to bring a smartphone to connect with VR360 and watch the video.
- Those who are willing to use their smartphone for research purposes (a smartphone will be provided by the research team if needed).
Exclusion Criteria:
- Individuals with hearing or vision impairments
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
The experimental group will receive AR/VR technology-based group training within a virtual clinical environment during their practicum
|
Students will receive AR/VR Technology and OSCE in a Virtual Clinical Environment to learn how to assess and manage patients with auditory hallucination.
The course was designed as a diverse and interactive learning experience, integrating a virtual clinical environment for auditory hallucinations with the application of Objective Structured Clinical Examination (OSCE).
The practicum lasts approximately 15 days, with 8 hours per day.
The teaching activities of the course will be held 5 times on days 4, 6, 8, 10, and 12 of the practicum.
Additionally, students will have access to the AR/VR materials for self-practice during the practicum.
|
|
Active Comparator: Control group
The control group will watch educational videos and participate in a general discussion group focused on auditory hallucinations.
|
Students will receive a traditional course on auditory hallucination assessment, which includes watching educational videos and participating in a general discussion group on auditory hallucinations.
The practicum lasts approximately 15 days, with 8 hours per day.
The teaching activities of the traditional course will be held 5 times on days 4, 6, 8, 10, and 12 of the practicum.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Auditory Hallucination Situational Involvement and Empathy
Time Frame: at baseline on day 2 or 3 of the 15-day practicum (T0) and on day 15 of the practicum, three days after the intervention has finished (T1)
|
To assess the impact of the intervention on empathy, Schutte and Stilinović's (2017) method was used, employing the Situational Scale of Empathetic Responses (SSER) with 15 items.
These are divided into two categories: ① Empathic Perspective Taking (7 items) and ② Empathic Concern (8 items).
Participants imagined interacting with a person hearing voices and rated the items on a 5-point Likert scale, from 'strongly disagree' (1) to 'strongly agree' (5).
Higher scores indicate greater empathy in auditory hallucination scenarios.
|
at baseline on day 2 or 3 of the 15-day practicum (T0) and on day 15 of the practicum, three days after the intervention has finished (T1)
|
|
OSCE Evaluation Form for Auditory Hallucination Assessment and Intervention
Time Frame: at baseline on day 2 or 3 of the 15-day practicum (T0) and on day 15 of the practicum, three days after the intervention has finished (T1)
|
This form is part of the "Application of AR/VR Technology and OSCE in a Virtual Clinical Environment" teaching practice project. Both the experimental and control groups will watch videos; however, the control group will watch standard videos, while the experimental group will use AR/VR technology within a virtual clinical environment. Both groups will be assessed using OSCE combined with the virtual clinical environment. The evaluation form, developed by the researcher, will undergo content validity review by experts once the videos are completed. Different versions of the virtual clinical environment and OSCE assessment will be used before and after the intervention. The study plans to develop four different versions, all of which will be reviewed by experts and piloted. |
at baseline on day 2 or 3 of the 15-day practicum (T0) and on day 15 of the practicum, three days after the intervention has finished (T1)
|
|
Self-Assessment Questionnaire on Confidence in Auditory Hallucination Assessment and Intervention
Time Frame: at baseline on day 2 or 3 of the 15-day practicum (T0) and on day 15 of the practicum, three days after the intervention has finished (T1)
|
This section consists of a self-designed questionnaire by the researcher, primarily aimed at measuring students' confidence levels before and after the implementation of the teaching intervention.
It includes 7 items and serves as a simple assessment tool.
|
at baseline on day 2 or 3 of the 15-day practicum (T0) and on day 15 of the practicum, three days after the intervention has finished (T1)
|
|
Nursing Students' Knowledge, Attitudes, and Perceived Empathy Toward Auditory Hallucinations
Time Frame: at baseline on day 2 or 3 of the 15-day practicum (T0) and on day 15 of the practicum, three days after the intervention has finished (T1)
|
This assessment tool, developed by Mawson (2014), consists of 11 items related to statements about knowledge, attitudes, and empathy toward auditory hallucinations.
Nursing students are asked to respond to these statements using a 5-point Likert scale, with responses ranging from "strongly agree" (5) to "strongly disagree" (1).
These statements remain unchanged in the questionnaire.
|
at baseline on day 2 or 3 of the 15-day practicum (T0) and on day 15 of the practicum, three days after the intervention has finished (T1)
|
Collaborators and Investigators
Investigators
- Study Chair: Chiu Yueh Yang, PhD, National Yang Ming Chiao Tung University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- NYCU113035AEF
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.
Clinical Trials on Randomized Controlled Trial
-
Chinese University of Hong KongCompletedRandomized Controlled Trial | OsteotomyHong Kong
-
Parc de Salut MarRecruitingRandomized Controlled TrialSpain
-
Assistance Publique - Hôpitaux de ParisUniversity of OxfordCompletedRandomized Controlled TrialUnited Kingdom, France
-
Universitat Autonoma de BarcelonaMinisterio de Economía y Competitividad, SpainRecruitingRandomized Controlled TrialSpain
-
Bahir Dar UniversityCompletedRandomized Controlled TrialEthiopia
-
Fujian Medical University Union HospitalRecruitinga Randomized Controlled TrialChina
-
Chinese PLA General HospitalCompletedDexmedetomidine | Randomized Controlled TrialChina
-
Suleyman Demirel UniversityRecruitingRandomized Controlled Trial | Postoperative Rehabilitation | Lumbar MicrodiscectomyTurkey (Türkiye)
-
M.D. Anderson Cancer CenterNot yet recruitingRandomized Controlled Trial | Perception | Communication Skills | ProfessionalismUnited States
-
US Department of Veterans AffairsCompletedSmoking Cessation | Randomized Controlled TrialUnited States
Clinical Trials on AR/VR technology-based training
-
Kaohsiung Medical University Chung-Ho Memorial...Completed
-
Stanford UniversityRecruitingVirtual Reality | Augmented RealityUnited States
-
Danderyd HospitalStiftelsen PromobilaNot yet recruitingAcquired Brain Injury (Including Stroke)Sweden
-
Haukeland University HospitalStockholm UniversityActive, not recruitingTechnology | Mental Health Issue | Adolescent DevelopmentNorway
-
Indiana UniversityIndiana University HealthRecruitingPost Intensive Care Unit Syndrome | Intensive Care Unit Delirium | Intensive Care Acquired Cognitive Impairment | Virtual Reality Cognitive TrainingUnited States
-
Stanford UniversityCompletedPain, Acute | Pain, NeuropathicUnited States
-
Kaohsiung Medical University Chung-Ho Memorial...Completed
-
Kaohsiung Medical University Chung-Ho Memorial...CompletedVirtual Reality | Augmented Reality | Oral Care PerformanceTaiwan
-
National Taiwan University HospitalRecruiting
-
The Hong Kong Polytechnic UniversityRecruiting