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Clinical Trials in China / NCT04534907
Starting soon Not applicable

The Effect of Immersive Virtual Reality Treatment With Cognitive Behaviour Therapy for Obsessive-Compulsive Disorder

NCT04534907 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Mental Health Center
Phase
Not applicable
Started
2025-12-01
Last updated
2025-05-25

Condition(s) studied

Obsessive-Compulsive DisorderVirtual Reality

Investigational drug(s) / intervention(s)

The combination of exposure and response prevention (ERP) and VRTraditional ERP

The combination of exposure and response prevention (ERP) and VR: The combination of exposure and response prevention (ERP) and VR aimed to investigate the combination of an immersive virtual reality environment (VRE) alongside therapist delivered CBT to reduce anxiety when the OCD patients were induced by virtual scene.Specially, patients will get the first CBT session in the first week for 90 minutes in order to gather detailed information of individual's symptom. Then the next 2 weeks, patients will get VR+ERP session twice a week. From the fourth week to the seventh week, patients weill get VR+ERP session once a week. In the end of the eighth week, patients will get the last session of the exposure-based CBT for relapse prevention.

Traditional ERP: Patients will achieve the exposure based CBT for total 10 times excluding 8 sessions of ERP. Structured protocol described by Foa et al., 2012. Specially, patients will get the first CBT session in the first week for 90 minutes in order to gather detailed information of individual's symptom. Then the next 2 weeks, patients will get ERP session twice a week. From the fourth week to the seventh week, patients weill get ERP session once a week. In the end of the eighth week, patients will get the last session of the exposure-based CBT for relapse prevention.

Study summary

This study will evaluate the clinical effectiveness ofthe Immersive Virtual Reality alongside exprosure and response Prevention (ERP) Treatment in cognitive-Behavioral Therapy for Obsessive-compulsive Disorder, and the underlying neural mechanism by electroencephalography (EEG) and eye-tracking methodology .

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * age: 18-50 years old; * Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for OCD; * Y-BOCS total score \> or = 16, discontinued medication for at least 8 weeks before * the enrollment or the paitients' clinical medication is stable for at least a month (the dose and the types of drugs) .\>or=9 years education Exclusion Criteria: * Any axis I psychiatric disorder comorbidity * Participants who have received any forms of psychological therapy in the past. * Patients cannot tolerate or adapt to the somatic discomfort caused by VR . * Prior history of neurological disease (e.g., epilepsy) or brain surgery for traumatic brain injury * Participants with claustrophobic, heart pacemaker, mechanical heart valve, mechanical implant such as an aneurysm clip, hip replacement, or any other pieces of metal that have accidentally entered their body. * Any current significant medical condition. * serious suicide risk

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Mental Health Center Shanghai Shanghai Municipality

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04534907 on ClinicalTrials.gov ↗ ← All trials in China