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The Feasibility of VR for OUD

The Feasibility of 3D Therapy Thrive for Inpatients With Opioid Use Disorder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06255119
Enrollment
40
Registered
2024-02-13
Start date
2022-10-18
Completion date
2023-12-31
Last updated
2024-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Use Disorder

Keywords

mood, cravings, retention

Brief summary

This study aims to evaluate feasibility of a virtual reality software device and measure the effects of the intervention on OUD patient mood, tension and cravings, as well as the effect of treatment on patient retention to their inpatient detox protocol.

Detailed description

The primary objective of this study is to evaluate the feasibility and preliminary effectiveness of a novel virtual reality (VR) based intervention; 3D Therapy Thrive (3DTT). Inpatient detoxification can improve outcomes for individuals with opioid use disorder (OUD), however patients often leave treatment early due to mood, tension, and cravings associated with opioid withdrawal. Subjects were recruited from a community inpatient detoxification program and received up to two sessions of 3DTT. The patients completed surveys to assess their mood, distress, cravings, and overall satisfaction with the experience. Retention was measured by protocol completion as reported by clinic staff, independent of the study. A group of patients with OUD consecutively admitted to the program comprised a comparison treatment-as-usual (TAU) group.

Interventions

DEVICE3D Therapy Thrive

A novel virtual reality software intervention that utilizes elements of Cognitive Behavioral Therapy to improve outcomes for inpatients with OUD.

Sponsors

3D Therapy, LLC
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
SINGLE (Subject)

Masking description

Subjects were blinded to study condition.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1.18 years or older 2\. Current diagnosis of opioid use disorder 3\. Current inpatient in detox ATS unit 4\. Fluent in English

Exclusion criteria

1. Active suicidality 2. History of seizures 3. History of psychosis 4. Severe visual impairment

Design outcomes

Primary

MeasureTime frameDescription
Retention in TreatmentAt departure from facility, through study completion, an average of 10 daysMedical record indicating whether patient completed detox protocol (i.e., completed, left against medical advice, administratively discharged, or moved to higher level of care)
Feasibility and Tolerability of 3DTTImmediately after each treatmentFeasibility and tolerability of 3DTT was measured by the Side Effects Questionnaire.

Secondary

MeasureTime frameDescription
MoodBefore and after each treatment, approximately every other day for up to 5 daysDepressive symptoms as measured by the AB-POMS depression scale (0-4, not at all to extremely)
AnxietyBefore and after each treatment, approximately every other day for up to 5 daysAnxiety symptoms as measured by the AB-POMS scale (0-4, not at all to extremely)
CravingsBefore and after each treatment, approximately every other day for up to 5 daysOpioid cravings as measured by the Visual Analog Scale (1-10, with higher scores indicating greater cravings.)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026