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Virtual Reality Exposure Therapy for Acrophobia

N

National Institute of Mental Health, Czech Republic

Status

Completed

Conditions

Fear of Heights
Specific Phobia
Acrophobia
Anxiety Disorders

Treatments

Other: Information Session
Behavioral: Exposure Therapy (Virtual Reality)

Study type

Interventional

Funder types

Other

Identifiers

NCT04975854
TL03000223-01

Details and patient eligibility

About

The aim of this study is to examine the efficacy of virtual reality exposure therapy (VRET) as a treatment for specific phobia (acrophobia). The study will randomly assign 42 participants with acrophobia to one of two conditions: a) the experimental condition (consisting of 3 sessions of virtual reality exposure) or b) a control condition. Both groups will receive short information session about general principles of exposure therapy before the start of the study. After the end of the study, the waitlist group will be invited to attend the short version (one or two-sessions) of the VRET. Both groups will receive a final follow-up questionnaires 2 months after the last session.

Enrollment

43 patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • individual meeting ICD-10 criteria for diagnosis of specific phobia
  • fluent in Czech

Exclusion criteria

  • currently receiving psychological treatment for acrophobia
  • psychotropic medication (unless on stable dosage for the previous 1 month and stabilized for the duration of the study)
  • another severe mental disorder, such as bipolar disorder or psychotic disorder
  • contradictions to using a virtual reality (e.g., epilepsy, balance problems)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

43 participants in 2 patient groups

Virtual Reality Exposure
Experimental group
Description:
Participants complete three 30-40-minute sessions of exposure administered via a virtual reality headset. The exposure involve exposure to various heights and height cues in the virtual city environment. Experimental group also attends 20-minute online information session (prerecorded video).
Treatment:
Other: Information Session
Behavioral: Exposure Therapy (Virtual Reality)
Control
Other group
Description:
Control group attends a single 20-minute information session (prerecorded video) about general principles of exposure therapy and anxiety before the start of the study, but receives no exposure-based intervention.
Treatment:
Other: Information Session

Trial contacts and locations

1

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Central trial contact

Iveta Fajnerova; Anna Francova

Data sourced from clinicaltrials.gov

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