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NCT05675735
Leveraging Regulatory Flexibility for Methadone Take-Home Dosing to Improve Retention in Treatment for Opioid Use Disorder
Conditions: Problems Related to Social Environment
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Phase: NA
Enrollment: 318
Sponsor: NYU Langone Health
Location: United States
Summary
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.
Eligibility Criteria
Inclusion Criteria: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:-- Anyone aged 18 or older who has been receiving take-home methadone for at least 30 days.Exclusion Criteria: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.
Source: ClinicalTrials.gov (NCT05675735). StuddyBuddy aggregates publicly available trial information.