REMOTE OBSERVED DOSING TO IMPROVE SUBOXONE COMPLIANCE IN CLINICAL PRACTICE
Brief description of study
REMOTE OBSERVED DOSING TO IMPROVE SUBOXONE COMPLIANCE IN
CLINICAL PRACTICE
If you suffer from opioid dependence, a new clinical
research study is available for you. This purpose of this research study is to see
whether remote observed dosing (i.e., video recordings) helps to improve
medication adherence.
Detailed description of study
The RODS study offers 12 weeks of Suboxone treatment.
Suboxone is an FDA approved medication used to treat opioid use disorder. While
the medication phase last 12 weeks, the study takes 15 weeks all together. You
will be under a clinician care throughout the course of the study. There is a
baseline screening visit that includes bloodwork, a urine drug test, physical
exam, and questionnaires. Participants will be randomly (similar to flipping
a coin) assigned to one of two groups: the remote observed dosing group or the
attention control group. The remote observed dosing group will submit daily
video recordings of themselves taking their Suboxone dose. The attention
control group will complete daily surveys confirming that they have taken their
daily Suboxone dose. Both groups receive 12-weeks of Suboxone as well as a
study phone with a capped talk, text, and data plan that is yours to keep
after study completion. Suboxone induction will occur across three hour-long visits.
Following induction, participants will come in twice a week for 30-45 minute study
visits. A urine sample will be collected at every visit.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
-
Conditions:
opioid use disorder
-
Age: Between 18 Years - 55 Years
-
Gender: All
Updated on
08 Jul 2023.
Study ID: 831410