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Digital Treatment for Chronic Pain and Addiction in Veterans With Opioid Use Disorder Receiving Buprenorphine

NCT ID: NCT07361432
Registry status: Not yet recruiting
Study type: Interventional
Phase: Phase 3
Sponsor: VA Office of Research and Development
Conditions: Chronic Pain, Opioid Use Disorder

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Improving Pain and Functioning Using an Integrative Digital Treatment for Chronic Pain and Addiction in Veterans With Opioid Use Disorder Receiving Buprenorphine

Enrollment: 250 participants (Estimated).

What is being studied

Behavioral: Enhanced Treatment as Usual (ETAU)
Behavioral: Integrating the Management of Pain and Addiction via Collaborative Treatment (IMPACT)

Who may be eligible

Ages: 18 Years to no maximum
Sex: All
Healthy volunteers accepted: No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * an ICD-11 opioid use disorder (OUD) diagnosis in the VHA electronic health record (EHR) * receipt of buprenorphine from outpatient addiction clinic with stable (i.e., unchanged in 2 weeks or since last injection) dose confirmed by the prescribing clinician. Both oral and injectable buprenorphine formulations will be eligible with dose stabilization required to isolate chronic pain from withdrawal-related pain associated with non-therapeutic dose * presence of musculoskeletal pain that is bothersome or high-impact per the Graded Pain Scale - Revised * access to a web-connected device to complete daily surveys and connect to Integrating the Management of Pain and Addiction via Collaborative Treatment (IMPACT) treatment site * ability to participate safely in the walking portion of the intervention as evidenced by patient-reported ability to walk at least one block Exclusion Criteria: * dementia-related electronic health record (EHR) diagnosis * participant-reported vision or hearing impairments that would preclude use of the Integrating the Management of Pain and Addiction via Collaborative Treatment (IMPACT) system * legal actions that would make study completion unlikely * current or past 12 month engagement in CBT for chronic pain treatment * planned surgical intervention for pain * physical or mental health conditions that would interfere with ability to meaningful engage in Integrating the Management of Pain and Addiction via Collaborative Treatment (IMPACT) and Medication for OUD (MOUD) treatment (e.g., uncontrolled bipolar disorder, active suicidal ideation, receipt of hospice or end-of-life palliative care)

Study locations

4 study locations are listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: United States

Connecticut, United States: 1
Massachusetts, United States: 2
Oregon, United States: 1

Sample of listed locations

VA Connecticut Healthcare System West Haven Campus, West Haven, CT — West Haven, Connecticut, 06516-2770, United States — Site recruitment status not specified in the registry data
VA Bedford HealthCare System, Bedford, MA — Bedford, Massachusetts, 01730-1114, United States — Site recruitment status not specified in the registry data
VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA — Boston, Massachusetts, 02130-4817, United States — Site recruitment status not specified in the registry data
VA Portland Health Care System, Portland, OR — Portland, Oregon, 97207-2964, United States — Site recruitment status not specified in the registry data

Study details

Start date: November 2, 2026
Primary completion date: June 3, 2029
Completion date: May 31, 2030
First posted: January 23, 2026

Source and update information

Source: ClinicalTrials.gov
NCT ID: NCT07361432
Registry last updated: September 17, 2026
QualifiedStudies registry data refreshed: September 28, 2026
QualifiedStudies record fetched: September 28, 2026

View NCT07361432 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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