Skip to content

Virtual Reality for Generalized Anxiety Disorders

A Randomized Control Trial of the Use of Virtual Reality as an Adjunct in the Treatment for Generalized Anxiety Disorders

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05895721
Acronym
VR-GAD
Enrollment
80
Registered
2023-06-09
Start date
2023-02-21
Completion date
2024-09-30
Last updated
2024-07-08

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

Conditions

Generalized Anxiety Disorder

Keywords

GAD, VR

Brief summary

The goal of this clinical trial is to apply Virtual Reality as an adjunct treatment for Generalized Anxiety Disorder. The main question it aims to answer are: * Determination of the efficacy of VR modules as an adjunct therapy in improving GAD-7 scores * Assessment of the acceptability of VR modules as an adjunct therapy to the standard of care Participants will randomized into two arms: * Control Arm: Standard of Care only * Intervention Arm: Standard of Care + VR Modules

Interventions

OTHERVirtual Reality

Virtual Reality as adjunct treatment

Sponsors

Clinical Research Centre, Malaysia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 59 Years
Healthy volunteers
No

Inclusion criteria

1. Age between 18-59 2. The primary diagnosis is a generalized anxiety disorder 3. Agree to participate and consented as per study protocol. 4. There is no change in the standard of care within the past two months prior to enrollment into the study. If a patient is on any psychotherapy, then there is no change in the type of current psychotherapy intervention. 5. GAD- 7 more than or equal to 5. 6. Able to come for the session as per scheduled.

Exclusion criteria

1. Documented or known case of permanent hearing/visual impairment e.g., vestibular abnormalities that represent significant contraindications for the use of VR or visual impairment e.g., cataract. 2. Documented Disorder as listed: * A. Psychosis * B. Psychosis disorder - previous case, known case of * C. Claustrophobia * D. Substance use * E. Personality disorder * F. Visual impairment that might hinder usage of virtual reality equipment * G. Intellectual disabilities * H. All types of seizures including febrile seizure 3. The patient is under more than 1 center during follow up (e.g., patient is also receiving treatment from a private hospital for GAD).

Design outcomes

Primary

MeasureTime frameDescription
To determine the efficacy of VR modules as an adjunct therapy in improving GAD-7 scores among patients with generalized anxiety disorders.Week 0 - Week 4Patient will be access with GAD-7 questionnaire repeatedly at different time interval (3 Times - Week 0, Week 2, Week 4) .

Secondary

MeasureTime frameDescription
To assess the acceptability of VR modules as an adjunct therapy to the standard of care among patients with generalized anxiety disorders.Week 0 - Week 4Patient will assess with standard questionnaire on acceptability of VR technology (3 Times - Week 0, Week 2, Week 4).

Countries

Malaysia

Outcome results

None listed

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