The Use of a Virtual Reality Intervention on Stigma, Empathy and Attitudes Towards People With Psychotic Disorders

October 9, 2023 updated by: Tay Jing Ling, Institute of Mental Health, Singapore

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

Recruiting

Conditions

Study Type

Interventional

Enrollment (Estimated)

180

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

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:

  • 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

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: 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
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
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

This is where you will find people and organizations involved with this study.

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, 2023

Primary Completion (Estimated)

July 17, 2024

Study Completion (Estimated)

July 17, 2024

Study Registration Dates

First Submitted

July 24, 2023

First Submitted That Met QC Criteria

August 1, 2023

First Posted (Actual)

August 8, 2023

Study Record Updates

Last Update Posted (Actual)

October 11, 2023

Last Update Submitted That Met QC Criteria

October 9, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2023/00027

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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