Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04978168

Opioid Treatment and Peer Recovery Support

Led by Brown University · Updated on 2025-05-13

450

Participants Needed

3

Research Sites

269 weeks

Total Duration

On this page

Sponsors

B

Brown University

Lead Sponsor

U

University of North Carolina, Chapel Hill

Collaborating Sponsor

AI-Summary

What this Trial Is About

Determine whether a facilitated local change team intervention improves a probation organization's client-level medication for opioid use disorder (MOUD) outcomes and implementation outcomes relative to baseline across multiple sites. Determine whether client-level outcomes are further enhanced by the introduction of Peer Support Services.

CONDITIONS

Official Title

Opioid Treatment and Peer Recovery Support

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Community provider staff who support MOUD clients, have an active caseload including individuals on probation, and commit to 12 months in the project
  • Probation officers with an active caseload willing to commit to 12 months in the project
  • Adults 18 years or older on probation within 90 days before enrollment
  • English speaking individuals
  • Diagnosed with opioid use disorder
  • Have a stable method of contact in the community
Not Eligible

You will not qualify if you...

  • Individuals on probation who are currently incarcerated or in court-mandated inpatient treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Duke University

Durham, North Carolina, United States, 27708

Actively Recruiting

2

Temple University

Philadelphia, Pennsylvania, United States, 19122

Actively Recruiting

3

Brown University

Providence, Rhode Island, United States, 02912

Actively Recruiting

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Research Team

R

Rosemarie A Martin, PhD

CONTACT

J

Jennifer Duff

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

3

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