- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05982548
The Use of a Virtual Reality Intervention on Stigma, Empathy and Attitudes Towards People With Psychotic Disorders
The Use of a Virtual Reality Intervention on Stigma, Empathy and Attitudes Towards People With Psychotic Disorders Among Mental Healthcare Professionals
The goal of this clinical trial is to evaluate the effectiveness of a VR intervention on (1) stigma, (2) empathy and (3) attitudes towards those experiencing mental disorders.
Participants will review a VR intervention, and complete questionnaires at pre-test, post-test and one month follow-up.
Researchers will compare the VR intervention with a control VR intervention to evaluate the varying effects on stigma, empathy and attitudes towards those experiencing mental disorders.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Singapore, Singapore, 539747
- Recruiting
- Institute of Mental Health
-
Contact:
- Jing Ling Tay, PhD
- Phone Number: 2337 6389
- Email: jing_ling_tay@imh.com.sg
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants who are aged at least 21 years old
- Employed by the Institute of Mental Health as a physician, allied health professional or nurse.
- understands English
- work directly with patients.
Exclusion Criteria:
- unable to use virtual reality interventions due to reasons including motion sickness, disorientation, nausea and vomiting.
- history of epilepsy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
The VR intervention was created using the Unreal Engine software (Unreal Engine, 2022). The VR intervention includes the scenario of a home. Participants will view the home as a first person character and experience psychotic phenomena including auditory hallucinations. The intervention will be delivered in one setting and lasts no more than seven minutes. It will be disseminated using smartphone inserted into VR headset equivalent of google cardboard. |
VR intervention of no more than 7 minutes Participants viewed the home as a first person character and experience psychotic phenomena including auditory hallucinations. |
|
Active Comparator: VR control group
The VR control group will view the scenario of the same home without the simulated visual and auditory hallucinations.
|
VR intervention of no more than 7 minutes Participants viewed the same home as a first person character without psychotic phenomena |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Desire for Social Distance
Time Frame: pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
|
Desire for Social Distance Scale The eight questions are rated on a four-point Likert scale: yes, definitely (0), yes, probably (1), probably not (2) and definitely not (3) with greater scores implying greater desire for social distancing. |
pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
|
|
Personal Stigma
Time Frame: pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
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Personal Stigma Scale Personal Stigma Scale consisted of two subscales: 'Personal unpredictable/ dangerousness' and 'Personal weak not sick' The questions were calculated as 'strongly agree' (4) to 'strongly disagree' (0), with greater scores implying greater stigmatizing attitudes.
|
pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
|
|
Empathy
Time Frame: pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
|
Empathetic concern sub-scale of Interpersonal Reactivity Index The 7-item sub-scale is measured on a five point likert scale ranging from 'does not describe me well' (0) to 'describes me very well' (4).
|
pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
|
|
Attitudes towards those experiencing mental disorders
Time Frame: pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
|
modified Attitudes Towards People with Schizophrenia scale The 7-item scale is measured on a nine point likert scale ranging from (1) to (9).
Greater scores equate better attitude towards people with schizophrenia.
|
pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Demographic data
Time Frame: pre-intervention
|
occupation, gender, marital status, ethnic groups, age, years of service
|
pre-intervention
|
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Acceptability of the intervention
Time Frame: immediately after the intervention
|
Authors constructed questionnaire to assess for acceptability of intervention. A total of 10 questions consisting of 6 multiple choice questions ranging from strongly disagree to strongly agree on a 7-point likert scale. An example of one question is, 'I find the intervention engaging'. It also consists of 4 open ended questions. Example of one question is, 'Please list the strength of the intervention' |
immediately after the intervention
|
|
Safety of VR intervention
Time Frame: immediately after the intervention
|
Visually induced motion sickness susceptibility questionnaire: It consists of six questions that evaluates presence of adverse effects from using the VR intervention from 'never' (0) to 'often' (3). |
immediately after the intervention
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
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
- 2023/00027
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
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