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Long-Term Treatment of Opioid Use Disorder

Long-Term Treatment of Opioid Use Disorder

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05534815
Enrollment
225
Registered
2022-09-10
Start date
2023-03-01
Completion date
2028-02-29
Last updated
2025-05-02

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

Conditions

Drug Addiction, Employment

Brief summary

Poverty and opioid addiction are interrelated and chronic problems which have not been addressed adequately. The Therapeutic Workplace could treat the many adults with opioid use disorder who are unemployed and live in poverty. The Therapeutic Workplace pays participants to work. To promote drug abstinence, the Therapeutic Workplace arranges employment-based abstinence reinforcement in which participants are required to provide drug-free urine samples to maintain maximum wages. Many studies have shown that employment-based abstinence reinforcement in the Therapeutic Workplace can promote and maintain drug abstinence. Recently, the investigators showed that abstinence-contingent wage supplements in the Therapeutic Workplace could promote drug abstinence and employment and reduce poverty. However, the investigators have not demonstrated the real-world impacts of the Therapeutic Workplace. The Therapeutic Workplace requires two modifications to produce real world impacts. 1. The investigators must develop a real-world version of the Therapeutic Workplace that community treatment programs can implement. 2. The investigators must reduce the costs of maintaining employment-based abstinence reinforcement. This application seeks to develop and evaluate a low-cost Therapeutic Workplace that community treatment programs can implement and that addresses the persistent nature of opioid addiction and poverty. The investigators propose to conduct a Stage III study in which a community clinic (REACH Health Services) adapts and implements the Therapeutic Workplace intervention. To improve the feasibility of this intervention, the investigators will use low-cost abstinence-contingent wage supplements to maintain abstinence. The investigators propose to conduct a randomized controlled study to evaluate the effectiveness of the low-cost abstinence-contingent wage supplements in a community Therapeutic Workplace to maintain long-term drug abstinence and employment, and to reduce poverty in adults with opioid use disorder. All participants will be invited to attend a 4-week induction period and 48 weeks of support by an employment specialist. At the end of a 4-week induction period, REACH unemployed methadone or buprenorphine patients with opioid use disorder who meet the Induction Period inclusion criteria (N=225) will be randomly assigned to a Usual Care Control, an Initiation Only, or an Initiation and Maintenance group. All groups will be offered methadone or buprenorphine treatment and an employment specialist for 48 weeks. Initiation Only and Initiation and Maintenance participants will earn high magnitude abstinence-contingent wage supplements during a 24-week Initiation period (weeks 1-24). Initiation and Maintenance participants will also earn low-magnitude abstinence-contingent wage supplements during a 24-week Maintenance period (weeks 25-48). The investigators will base the primary outcome measures on assessments conducted every four weeks of the Maintenance period. If low-cost abstinence-contingent wage supplements in the community Therapeutic Workplace maintain drug abstinence and employment and decrease poverty, community drug abuse treatment clinics could apply this intervention widely as a long-term maintenance treatment for unemployed adults with opioid use disorder.

Interventions

BEHAVIORALEmployment-based abstinence reinforcement

Participants will earn stipends for working with the employment specialist and wage supplements for working in a community job, but the stipends and wage supplements will depend on providing drug-free urine samples.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Northern Michigan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* ≥18 years old * are enrolled at REACH for buprenorphine or methadone maintenance treatment * unemployed

Exclusion criteria

* Applicants will be excluded if they report recent hallucinations and if they are currently a prisoner.

Design outcomes

Primary

MeasureTime frameDescription
Rate of Drug abstinence as assessed by a yes or no4 weeksWe will assess rate of urine samples negative for opioids (morphine, oxycodone, and fentanyl) and cocaine at the 4-week assessments during the Maintenance period. Y/N at each assessment).
Rate of Employment as assessed by a yes or no4 weeksWe will assess rate that participants report employment at the 4-week assessments conducted during the Maintenance period. Y/N at each assessment.

Countries

United States

Contacts

Primary ContactForrest Toegel, PhD
ftoegel@nmu.edu906-227-2919

Outcome results

None listed

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