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RecruitingNCT05982548Updated Oct 11, 2023

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

An interventional study of VR intervention and VR control intervention in Mental Disorder, sponsored by Institute of Mental Health, Singapore. Recruiting at 1 site in Singapore. Open to participants aged 21 Years to 99 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-10-11.

Sponsored by Institute of Mental Health, Singapore · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Jul 2024, 2 years 2 months ago, but the record still lists the study as recruiting.
  • Started Aug 2023; still recruiting 3 years 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
180
Allocation
Randomized
Ages
21 Years to 99 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Mental Disorder
03

In context

Mental Disorders

2,107 studies on the registry are indexed under Mental Disorders; 416 are open to participants now.

This study's planned enrollment of 180 is above the median of 94 across 1,574 interventional studies indexed under Mental Disorders.

Browse Mental Disorders studies →

Lead sponsor

Institute of Mental Health, Singapore is the lead sponsor of 16 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 99 Years
Sexes eligible
All
Accepts 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

Exclusion Criteria:

  • unable to use virtual reality interventions due to reasons including motion sickness, disorientation, nausea and vomiting.
  • history of epilepsy
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
180 participants (estimated)

Study arms

  • 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.

    Other: VR intervention

  • Active comparator
    VR control group

    The VR control group will view the scenario of the same home without the simulated visual and auditory hallucinations.

    Other: VR control intervention

Interventions

  • OtherVR intervention

    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

06

What researchers measure

Primary outcomes

  1. Desire for Social Distance

    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.

    Time frame: pre-intervention, immediately after the intervention, follow-up at 1 month after intervention

  2. Personal Stigma

    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.

    Time frame: pre-intervention, immediately after the intervention, follow-up at 1 month after intervention

  3. Empathy

    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).

    Time frame: pre-intervention, immediately after the intervention, follow-up at 1 month after intervention

  4. Attitudes towards those experiencing mental disorders

    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.

    Time frame: pre-intervention, immediately after the intervention, follow-up at 1 month after intervention

Secondary outcomes

  1. Demographic data

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

    Time frame: pre-intervention

  2. Acceptability of 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'

    Time frame: immediately after the intervention

  3. Safety of VR 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).

    Time frame: immediately after the intervention

07

Study locations

1 of 1 sites recruiting
  • Institute of Mental Health
    Singapore, 539747, Singapore
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 11, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05982548
Lead sponsor
Institute of Mental Health, Singapore
Responsible party
Tay Jing Ling (Advanced Practice Nurse, Institute of Mental Health, Singapore) — Principal investigator
First posted
Aug 8, 2023
Start date
Aug 1, 2023
Primary completion
Jul 17, 2024 (estimated)
Completion
Jul 17, 2024 (estimated)
Last update
Oct 11, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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