Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06845488

Application of Virtual Reality Technology to Treatment of Social Anxiety in Adults with Autism Spectrum Disorder

Led by The University of Texas Health Science Center, Houston · Updated on 2025-07-15

40

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating treatments for adults with autism and social anxiety disorder to compare two types of cognitive behavioral therapy (CBT). One approach combines CBT with virtual reality (VR) exposure and VR social skills training, while the other uses CBT with imaginal exposure and mindfulness. The study aims to determine which approach better reduces social anxiety severity, identify who benefits most from VR-based therapy, and assess how acceptable and feasible the VR treatment is for patients. This research is sponsored by The University of Texas Health Science Center, Houston. Participants will receive 12 weeks of weekly CBT sessions. One group will use VR software called the Virtual Communicator, featuring realistic avatars controlled by a therapist for interactive social practice over the internet without needing a headset. The other group will receive traditional CBT involving imaginal exposure and mindfulness techniques. Both treatments focus on reducing social anxiety and improving conversational skills. The VR sessions can be conducted in English or Spanish, increasing accessibility. During the study, participants’ anxiety levels will be measured at multiple points: baseline, 3, 6, 9, and 12 weeks, and about 4 weeks after treatment ends. Researchers will assess anxiety using several scales specific to social anxiety disorder. Participants must be verbal and literate in English or Spanish and able to operate a computer. The study carefully monitors outcomes and treatment acceptability over the 12-week intervention and follow-up period, with no masking or randomization involved.

CONDITIONS

Brief Title

Application of Virtual Reality Technology to Treatment of Social Anxiety

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with Autism Spectrum Disorder by a qualified professional
  • Verbal and literate in English or Spanish
  • Have average or greater intellectual ability based on history and interview
  • Able to operate a Windows or Mac computer
Not Eligible

You will not qualify if you...

  • Current or past severe mental illness such as schizophrenia, bipolar disorder, or severe depression
  • Intellectual disability or learning disability that would interfere with participation
  • Unable to use or access the required technology
  • Unable to read English or Spanish materials or instructions
  • Not able to operate a computer as required for the study procedures
  • Severe cognitive or reading impairments that prevent participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Outpatient Treatment

Duration - 12 weeks

Participants receive 12 weeks of weekly Cognitive Behavioral Therapy (CBT) for Social Anxiety. Those in the experimental group also use Virtual Reality software to practice social interactions and exposures as part of their therapy.

Weekly visits (in-person or remote) for 12 weeks

Follow-up

Duration - About 4 weeks

Participants are assessed approximately 4 weeks after completing treatment to evaluate changes in social anxiety symptoms.

1 follow-up visit (in-person or remote)

Trial Site Locations

Total: 1 location

1

The University of Texas Health Science Center at Houston

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

K

Katherine Loveland, PhD

C

Craig Motsenbocker, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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