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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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05982548
Enrollment
180
Registered
2023-08-08
Start date
2023-08-01
Completion date
2024-07-17
Last updated
2023-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Disorder

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.

Interventions

VR intervention of no more than 7 minutes Participants viewed the home as a first person character and experience psychotic phenomena including auditory hallucinations.

OTHERVR control intervention

VR intervention of no more than 7 minutes Participants viewed the same home as a first person character without psychotic phenomena

Sponsors

Institute of Mental Health, Singapore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
21 Years to 99 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Desire for Social Distancepre-intervention, immediately after the intervention, follow-up at 1 month after interventionDesire 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 interventionPersonal 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 interventionEmpathetic 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 interventionmodified 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

MeasureTime frameDescription
Acceptability of the interventionimmediately after the interventionAuthors 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'
Safety of VR interventionimmediately after the interventionVisually 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).
Demographic datapre-interventionoccupation, gender, marital status, ethnic groups, age, years of service

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026