← Back to Clinical Trials
Recruiting NCT06845488

NCT06845488 Application of Virtual Reality Technology to Treatment of Social Anxiety

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06845488
Status Recruiting
Phase —
Sponsor The University of Texas Health Science Center, Houston
Condition Autism Spectrum Disorder
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2024-11-07
Primary Completion 2026-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
CBTVR

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 40 participants in total. It began in 2024-11-07 with a primary completion date of 2026-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to compare CBT VR exposure + VR social skills treatment to CBT Imaginal exposure + mindfulness, in reducing the severity of social anxiety in adults with autism and social anxiety (SA), to identify characteristics associated with benefitting from the CBT-VR treatment and to assess acceptability and feasibility of the VR intervention for patients receiving it and use findings to improve methods and to prepare for a community based pragmatic trial.

Eligibility Criteria

Inclusion Criteria: * Autism Spectrum Disorder (ASD) (diagnosed by a qualified professional) * verbal and literate in English or Spanish * average or greater intellectual ability, based on history and interview * able to operate a computer (Windows or Mac). Exclusion Criteria: * current or historical severe mental illness such as schizophrenia, bipolar disorder, or severe depression * intellectual disability or a learning disability that would interfere with participating (e.g., unable to read) * unable use the technology or do not have access to the technology * unable to read

Contact & Investigator

Central Contact

Katherine Loveland, PhD

✉ Katherine.A.Loveland@uth.tmc.edu

📞 713-486-2587

Principal Investigator

Katherine Loveland, PhD

PRINCIPAL INVESTIGATOR

The University of Texas Health Science Center at Houstom

Frequently Asked Questions

Who can join the NCT06845488 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Autism Spectrum Disorder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06845488 currently recruiting?

Yes, NCT06845488 is actively recruiting participants. Contact the research team at Katherine.A.Loveland@uth.tmc.edu for enrollment information.

Where is the NCT06845488 trial being conducted?

This trial is being conducted at Houston, United States.

Who is sponsoring the NCT06845488 clinical trial?

NCT06845488 is sponsored by The University of Texas Health Science Center, Houston. The principal investigator is Katherine Loveland, PhD at The University of Texas Health Science Center at Houstom. The trial plans to enroll 40 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology