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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05982548
Other study ID # 2023/00027
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2023
Est. completion date July 17, 2024

Study information

Verified date October 2023
Source Institute of Mental Health, Singapore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date July 17, 2024
Est. primary completion date July 17, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 99 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Singapore Institute of Mental Health Singapore

Sponsors (1)

Lead Sponsor Collaborator
Institute of Mental Health, Singapore

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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.
pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
Primary 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. pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
Primary 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). pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
Primary 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. pre-intervention, immediately after the intervention, follow-up at 1 month after intervention
Secondary Demographic data occupation, gender, marital status, ethnic groups, age, years of service pre-intervention
Secondary 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'
immediately after the intervention
Secondary 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).
immediately after the intervention
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