Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
NCT07206199

Virtual Reality Exposure Therapy for Obsessive-Compulsive Disorder: Outpatients Trial

Led by National Institute of Mental Health, Czech Republic · Updated on 2025-10-03

30

Participants Needed

1

Research Sites

158 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). This study focuses on patients receiving treatment in outpatient psychiatry or clinical psychology settings, utilizing a within-subject design for comparison. Patients first complete informed consent and baseline questionnaires and are placed on a waiting list for five weeks. After this period, they are reassigned to the active (experimental) group, which will receive five sessions of exposure therapy in virtual reality over a subsequent five-week period. 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: Outpatients Trial

Who Can Participate

Age: 18Years - 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

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Trial Site Locations

Total: 1 location

1

Nationa Institute of Mental Health

Klecany, Česká Republika, Czechia, 250 67

Actively Recruiting

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Research Team

I

Iveta Hocko Fajnerová

CONTACT

P

Pavla Stopková

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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