MySafeRx™: An Integrated Mobile Platform for Buprenorphine Adherence
Completed · Not applicable
Conditions studied: Opioid Use Disorder
In brief
The goal of the MySafeRx study is to evaluate the feasibility, acceptability, and usability of a novel platform that integrates text messaging reminders, secure electronic pill organizers, and daily remote brief motivational recovery support visits with a standardized protocol for supervised self- administration of buprenorphine via videoconferencing.
Key facts
- Study ID
- NCT02778282
- Run by
- Dartmouth-Hitchcock Medical Center
- People needed
- 27
- Starts
- 2017-03-24
- Expected to finish
- 2021-08-31
- Last updated by the study team
- 2021-10-05
Who can join
Age: 18 and older, up to 39. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Women and men age 18-39, inclusive, who are competent, wish to participate and willing to provide informed consent.
- DSM-V diagnosis of opioid use disorder, moderate or severe
- Seeking to initiate buprenorphine treatment or currently receiving buprenorphine treatment but had recent positive illicit opioid urine toxicology or missed scheduled urine toxicology.
You may not qualify if…
- DSM-V diagnosis of dementia, neurodegenerative disease, or other organic mental disorder, mental retardation, or autism.
- Substantial cognitive impairment (Montreal Cognitive Assessment < 25/30)
- Currently homeless
- Actively homicidal or suicidal with an imminent plan
- Serious unstable medical illness including, cardiovascular, hepatic, renal, respiratory, endocrine, neurological, or hematological disease such that hospitalization for treatment of that illness is likely within the next 3 months.
Where it is running
- Cambridge Health Alliance Outpatient Addiction Services — Somerville, Massachusetts, United States
- Hawthorn Recovery Center — Bennington, Vermont, United States
- Mount Anthony Primary Care — Bennington, Vermont, United States
Full record on ClinicalTrials.gov
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