Contingency Management for Opioid and Stimulant Use Disorders in Primary Care

Sponsor
University of Minnesota (Other)
Overall Status
Recruiting
CT.gov ID
NCT05288751
Collaborator
(none)
200
1
3
21
9.5

Study Details

Study Description

Brief Summary

Contingency management (CM) is a behavioral intervention that involves incentivizing participants for target behaviors in a clinical setting. When applied to the treatment of substance use disorders, it has demonstrated efficacy in reducing the number of urine toxicology screens positive for illicit substances and increased engagement in treatment programs. However, there is a need to translate CM treatment to primary care settings. This study will implement and assess a CM program for patients with opioid use disorder, with or without comorbid stimulant use disorder, initiating outpatient addiction medicine services at a family medicine residency clinic. Eligible patients will earn monetary incentives for attending addiction medicine appointments and abstaining from substances during outpatient treatment. Data gathered from this pilot program will be used to improve patient outcomes, treatment, and retention for persons receiving medications for opioid use disorder (MOUDs) in a primary care setting.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Contingency Management
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Contingency Management as a Treatment for Opioid Use Disorder and Stimulant Use Disorder in a Primary Care Setting
Actual Study Start Date :
Jun 15, 2022
Anticipated Primary Completion Date :
Sep 16, 2023
Anticipated Study Completion Date :
Mar 16, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Treatment as usual (TAU)

These patients will not be assigned to the CM programs, but will be invited to complete study measures at the same time points: baseline, 3-months, 6-months, and 12-months.

Experimental: Attendance-only CM

Patients in this arm complete an appointments with his or her primary care provider (PCP) or member of the PCP's microteam . These appointments must be initiated by the PCP/microteam in accordance with the patient's treatment plan for regular follow-up appointments.

Behavioral: Contingency Management
Contingency management (CM) is a behavioral intervention that involves incentivizing participants for target behaviors in a clinical setting.

Experimental: Attendance + abstinence CM

Patients who test stimulant-positive during the initial urine drug screen (UDS) at their intake visit will be invited to additionally enroll in the abstinence CM schedule. All of the attendance-only CM rules described previously will apply to patients in the attendance + abstinence program.

Behavioral: Contingency Management
Contingency management (CM) is a behavioral intervention that involves incentivizing participants for target behaviors in a clinical setting.

Outcome Measures

Primary Outcome Measures

  1. Preliminary efficacy of CM on clinical outcomes: Visit Frequency [30 days post-intervention]

    Number of completed clinical visits per patient during the CM program.

  2. Preliminary efficacy of CM on clinical outcomes: Urine toxicology [30 days post-intervention]

    Percentage of UDS results that are negative for stimulants during the CM intervention period.

  3. Feasibility of CM for OUD in primary care: Recruitment [30 days post-intervention]

    percentage of patients invited to participate enroll in the treatment intervention.

  4. Feasibility of CM for OUD in primary care: Retention [30 days post-intervention]

    Of those patients who enroll in the intervention study, the percent that complete the CM intervention period.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • At least 18 years of age

  • Diagnosis of Opioid Use Disorder and/or Stimulant Use Disorder

  • Recently initiated medications for opioid use disorder (MOUDs) at Broadway Family Medicine (BFM), within 2 weeks of recruitment

  • Have an active prescription for buprenorphine-naloxone (Suboxone)

Exclusion Criteria:
  • Prescription for an amphetamine would exclude patients from the abstinence-based CM, but they could participate in the attendance-only CM.

  • Dementia, development disabilities, or cognitive functioning that is too low to participate in study measures, as determined by chart review and consultation with overseeing physician.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Minnesota Minneapolis Minnesota United States 55455

Sponsors and Collaborators

  • University of Minnesota

Investigators

  • Principal Investigator: Robert Levy, MD, University of Minnesota

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Minnesota
ClinicalTrials.gov Identifier:
NCT05288751
Other Study ID Numbers:
  • FMCH-2022-30581
First Posted:
Mar 21, 2022
Last Update Posted:
Jun 21, 2022
Last Verified:
Jun 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Minnesota
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 21, 2022