MySafeRx & MedicaSafe Open-Label Buprenorphine Induction and Lapse Evaluation (MyMOBILE)

Completed · Not applicable

Conditions studied: Opioid Use Disorder

In brief

The goal of the MyMOBILE 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
NCT02942199
Run by
Cambridge Health Alliance
People needed
12
Starts
2016-11-01
Expected to finish
2018-08-31
Last updated by the study team
2018-12-12

Who can join

Age: 18 and older, up to 39. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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