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

Not Applicable
Recruiting
Conditions
Mental Disorder
Interventions
Other: VR intervention
Other: VR control intervention
Registration Number
NCT05982548
Lead Sponsor
Institute of Mental Health, Singapore
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
180
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 & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupVR interventionThe 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 control groupVR control interventionThe VR control group will view the scenario of the same home without the simulated visual and auditory hallucinations.
Primary Outcome Measures
NameTimeMethod
Desire for Social Distancepre-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.

Personal Stigmapre-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.

Empathypre-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).

Attitudes towards those experiencing mental disorderspre-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.

Secondary Outcome Measures
NameTimeMethod
Acceptability of the interventionimmediately 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'

Demographic datapre-intervention

occupation, gender, marital status, ethnic groups, age, years of service

Safety of VR interventionimmediately 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).

Trial Locations

Locations (1)

Institute of Mental Health

🇸🇬

Singapore, Singapore

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