Leveraging Regulatory Flexibility for Methadone Take-Home Dosing to Improve Retention in Treatment for Opioid Use Disorder
Recruiting now · Not applicable
Conditions studied: Problems Related to Social Environment
In brief
Using a stepped-wedge randomized controlled trial, the study will test whether a clinic-level multidimensional intervention conducted in 36 opioid treatment programs (OTPs) will improve clinical decision making, regulatory confusion, legal liability concerns, capacity for clinical practice change, and financial barriers to take- home dosing (THD) for methadone as compared to treatment as usual.
Key facts
- Study ID
- NCT05675735
- Run by
- NYU Langone Health
- People needed
- 318
- Starts
- 2023-01-27
- Expected to finish
- 2027-08-31
- Last updated by the study team
- 2026-01-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Clinic staff inclusion will include anyone who works at the 10 clinics that the OASAS client data system generates from the quantitative analysis in year one. In years 2-5, clinics chosen by the OASAS client data system will be placed into six cohorts. Only staff from these clinics will be eligible.
- Patient inclusion will include anyone aged 18 or older who has been receiving take-home methadone for at least 30 days.
You may not qualify if…
- There are no exclusion criteria related to sex/gender to increase the generalizability of the findings. The investigators will note include children in this study because the treatment system that we are examining largely excludes adolescents and younger children.
Where it is running
- University of Connecticut — Storrs, Connecticut, United States (enrolling)
- University at Buffalo — Buffalo, New York, United States (enrolling)
- NYU Langone Health — New York, New York, United States (enrolling)
- Weill Cornell Medical College — New York, New York, United States (enrolling)
Full record on ClinicalTrials.gov
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