About this trial
This study will compare in-person induction and maintenance dosing of sublingual buprenorphine to induction and maintenance dosing of sublingual buprenorphine through comprehensive telehealth sessions and telehealth medication for opioid use disorder (MOUD).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
meet DSM-5 criteria for OUD
Voluntarily seeking buprenorphine treatment for OUD
Able to provide informed consent and comply with study procedures
Disqualifiers
Meeting DSM-5 criteria for substance use disorder other than opioid as the primary diagnosis that would compromise safety of participation in the trial as determined by the study physician, such as an alcohol or sedative hypnotic use disorder that requires detoxification
Having a comorbid psychiatric diagnosis that might interfere with participation or make participation hazardous, such as a psychotic disorder including schizophrenia or schizoaffective disorder
Concurrent methadone, buprenorphine, or vivitrol maintenance treatment
Known history of allergy, intolerance, or hypersensitivity to candidate medication (buprenorphine)
Trial design
Parallel
Treatments tested in this trial
Buprenorphine SL
DrugUp to 24 mg per day
Telehealth
Other interventionTelehealth MOUD, utilizing a standardized protocol for each healthcare provider session
In-person treatment as usual
Other interventionin-person induction and maintenance dosing of sublingual buprenorphine, or MOUD as usual.
Treatment groups
Trial outcomes
Primary outcomes
Time to drop out
Comparing time to drop out between the treatment arms
Locations
Sponsors and contacts
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New York State Psychiatric Institute
Lead sponsor
National Institute on Drug Abuse (NIDA)
Collaborator
This trial is not recruiting at the moment. You can still explore other options: