Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03636022 · ClinicalTrials.gov registry record · NA

Virtual Reality System for Anxiety and OCD

A NA study, sponsored by Minnesota HealthSolutions.

Completed
Registry status
NA
Development phase
45
Enrollment target

NCT03636022: Completed NA study, sponsored by Minnesota HealthSolutions.

NCT03636022 is a NA study that has completed, run by Minnesota HealthSolutions. The registered enrollment target is 45 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03636022, a NA study, has completed, sponsored by Minnesota HealthSolutions.

COMPLETED
Registry status
NA
Development phase
45 participants
Enrollment target

Study Summary

Cognitive Behavioral Therapy with fear provoking exposures is the most effective therapy for anxiety disorders. The investigators aim to enhance this therapy with the use of virtual reality exposures. The human subjects study will test the effects of using VR for exposures compared to traditional imaginal exposures on anxiety symptom improvement, functioning, child engagement in an response to exposures, completion of exposure homework between treatment sessions, and length of treatment in weeks and length of treatment among children with anxiety disorders and/or obsessive compulsive disorder. The funding award supports the development of the technology and the human subjects study. The subcontract to Mayo supports expert input to identify clinically relevant content for therapeutic videos on the VR system and the human subjects study to test the VR system.

Primary Outcome

The SUDS - 0 to 10 ratings, where 0 indicates that participants feel no anxiety at all and 10 indicates that participants are experiencing maximum distress. The mean change in SUDS during the Session VR exposure versus mean change in SUDS during the conventional (control condition) verbal imaginal exposure.

Interventions

  • OTHER Control
  • OTHER VR System

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2020-11-01
Est. Completion 2023-05-31
Phase NA
Minnesota HealthSolutions

9 total trials

What the finished NCT03636022 record still lists

NCT03636022 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which Control is the first listed.

NCT03636022 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03636022 about?

NCT03636022 is a clinical study titled "Virtual Reality System for Anxiety and OCD". Cognitive Behavioral Therapy with fear provoking exposures is the most effective therapy for anxiety disorders. The investigators aim to enhance this therapy with the use of virtual reality exposures. The human subjects study will test the effects of using VR for exposures compared to traditional im...

What is the current status of trial NCT03636022?

This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2020-11-01. Estimated completion is 2023-05-31.

What interventions are being tested in trial NCT03636022?

The interventions under investigation include: Control (OTHER), VR System (OTHER).

Who is sponsoring clinical trial NCT03636022?

This trial is sponsored by Minnesota HealthSolutions, which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03636022's enrollment target sits among peer trials

45 1411th of 2000 higher than 578 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00804154 · 45 participants · Phase 1

    Resiniferatoxin to Treat Severe Pain Associated With Advanced Cancer

  • NCT01851694 · 45 participants · NA

    Beta-cell Response to Incretin Hormones in Cystic Fibrosis

  • NCT02896335 · 45 participants · Phase 2

    Palbociclib and Pembrolizumab In Central Nervous System Metastases

  • NCT03454035 · 45 participants · Phase 1

    Ulixertinib/Palbociclib in Patients With Advanced Pancreatic and Other Solid Tumors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03636022, the US trial registry maintained by the National Library of Medicine. NCT03636022 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.