Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05973838

Peer-Delivered Behavioral Activation Intervention to Improve Polysubstance Use and Retention in Telemedicine Opioid Use Disorder Treatment in Underserved Areas

Led by University of Maryland, College Park · Updated on 2026-04-27

160

Participants Needed

4

Research Sites

8 weeks

Total Duration

On this page

Sponsors

U

University of Maryland, College Park

Lead Sponsor

U

University of Maryland, Baltimore

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to evaluate a peer-led, brief behavioral intervention designed to improve medication adherence for opioid use disorder (MOUD) and reduce polysubstance use among patients with opioid use disorder (OUD) and polysubstance use in underserved areas. The study focuses on a behavioral activation (BA) approach delivered by trained peer recovery specialists (PRSs) and compares it to treatment as usual (TAU) over a 12-month period. The trial addresses challenges in OUD treatment retention, especially in communities with limited access to addiction care and rising stimulant use. Participants will be randomly assigned to either the Peer Activate intervention or enhanced treatment as usual. Those in the Peer Activate group will receive about six weekly core sessions, lasting 30 minutes to one hour, led by PRSs teaching behavioral activation and problem-solving skills. Additionally, up to six optional booster sessions are available to reinforce these skills. The TAU group receives standard telemedicine services enhanced with community referrals and follow-ups, plus regular meetings with addiction medicine physicians and PRSs for general support. Throughout the study, participants will be monitored with urinalysis and self-reports to assess polysubstance use, treatment retention, and medication adherence over six months. Researchers will also track intervention attendance, uptake, and fidelity. The trial includes multiple assessments to measure problems related to substance use and the effectiveness of peer-delivered behavioral activation in improving outcomes for patients receiving telemedicine buprenorphine treatment. Total participation and follow-up last at least 12 months.

CONDITIONS

Brief Title

Peer Recovery to Improve Polysubstance Use and Mobile Telemedicine Retention

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be 18 years of age or older
  • Receive opioid use disorder treatment as part of a telemedicine program
  • Have used one or more non-prescribed substances (excluding opioids and tobacco) in the past three months by urine test or self-report
Not Eligible

You will not qualify if you...

  • Have active, unstable, or untreated psychiatric symptoms such as mania or psychosis that interfere with participation
  • Unable to understand the study or provide informed consent in English

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)

Treatment

Duration - Approximately 12 weeks

Participants receive peer-delivered behavioral activation sessions to support opioid use disorder treatment retention and reduce polysubstance use. This includes about six weekly core sessions and up to six optional booster sessions.

Weekly sessions for up to 12 weeks

Follow-up

Duration - Up to 6 months

Participants are followed for ongoing assessment of treatment retention, substance use, and adherence over six months after starting the intervention.

Regular assessments during the 6-month follow-up period

Trial Site Locations

Total: 4 locations

1

HIPS Clinic

Washington D.C., District of Columbia, United States, 20002

Not Yet Recruiting

2

University of Maryland Baltimore (UMD Drug Treatment Center)

Baltimore, Maryland, United States, 21223

Not Yet Recruiting

3

University of Maryland, College Park

College Park, Maryland, United States, 20742

Not Yet Recruiting

4

Caroline County Behavioral Health

Denton, Maryland, United States, 21629

Actively Recruiting

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Research Team

M

Morgan S Anvari, BA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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https://pubmed.ncbi.nlm.nih.gov/21310539

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An initial randomized controlled trial of behavioral activation for treatment of concurrent crystal methamphetamine dependence and sexual risk for HIV acquisition among men who have sex with men.

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https://pubmed.ncbi.nlm.nih.gov/30887824

The effect of a behavioral activation treatment for substance use on post-treatment abstinence: a randomized controlled trial.

Stacey B Daughters, Jessica F Magidson, Deepika Anand...

https://pubmed.ncbi.nlm.nih.gov/28963853

Implementing Behavioral Activation and Life-Steps for Depression and HIV Medication Adherence in a Community Health Center.

Jessica F Magidson, C J Seitz-Brown, Steven A Safren...

https://pubmed.ncbi.nlm.nih.gov/25419102

"Someone who is in this thing that I am suffering from": The role of peers and other facilitators for task sharing substance use treatment in South African HIV care.

Jessica F Magidson, John A Joska, Kristen S Regenauer...

https://pubmed.ncbi.nlm.nih.gov/31082664

ACT HEALTHY: A Combined Cognitive-Behavioral Depression and Medication Adherence Treatment for HIV-Infected Substance Users.

Stacey B Daughters, Jessica F Magidson, Randi M Schuster...

https://pubmed.ncbi.nlm.nih.gov/21709737

An Initial Open Trial of a Brief Behavioral Activation Treatment for Depression and Medication Adherence in HIV-Infected Patients.

Matthew T Tull, Christopher R Berghoff, Joseph R Bardeen...

https://pubmed.ncbi.nlm.nih.gov/28799413