Actively Recruiting

Phase Not Applicable
Age: 17Years - 55Years
All Genders
NCT07245134

Virtual Reality Exposure Therapy for Obsessive-Compulsive Disorder: A Randomized Controlled Trial in Inpatients

Led by National Institute of Mental Health, Czech Republic · Updated on 2025-11-24

62

Participants Needed

1

Research Sites

215 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to evaluate the efficacy of virtual reality exposure therapy (VRET) as a treatment for obsessive-compulsive disorder (OCD). Participants are randomly assigned to one of the following interventions: a) exposure condition - the group with a standard CBT program enriched with exposure therapy in VR (VRET), b) control condition 1 - the group with a standard CBT program enriched with VR cognitive training aimed at cognitive flexibility or c) control condition 2 - standard CBT program without any additional VR intervention. The treatment effect will be evaluated using pre/post assessments, as well as monitoring adherence to exposure and response prevention assignments.

CONDITIONS

Official Title

Virtual Reality Exposure Therapy for Obsessive-Compulsive Disorder: A Randomized Controlled Trial in Inpatients

Who Can Participate

Age: 17Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of OCD (F42) using currently valid DSM-V and ICD-11
  • Fluent in Czech
Not Eligible

You will not qualify if you...

  • Any other psychiatric, neurological and serious somatic illness
  • Substance abuse
  • Psychotropic medication (e.g. benzodiazepines) except antidepressants, antipsychotic medication and hypnotics
  • Contradictions to using a virtual reality (e.g., epilepsy, balance problems)
  • Pregnancy
  • Cardiostimulator and mental implants

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

National Institute of Mental Health

Klecany, Czechia

Actively Recruiting

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Research Team

I

Iveta Fajnerová

CONTACT

P

Pavla Stopková

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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