Remote Opioid Use Disorder Research Study
Researchers at the Medical University of South Carolina (MUSC) are conducting a study on improving sleep for individuals receiving medication-assisted treatment for opioid use disorder.
Fast Facts
Initiated or Modified Dose of Buprenorphine (Suboxone or Subutex) Treatment in The Last 3 Months
Experience Poor Sleep Quality
Compensation
Provided
Conducted Remotely Nationwide
Study Background
Poor sleep is common among individuals receiving treatment for opioid use disorder, but there are few effective, accessible solutions.
This study aims to develop and test a mobile health (mHealth) behavioral sleep intervention app designed specifically for people receiving medications such as buprenorphine. The app uses evidence-based strategies from behavioral sleep medicine to help participants track and improve their sleep patterns.
By engaging with the app over several weeks, participants will contribute valuable feedback that will help researchers refine and evaluate the program’s effectiveness in improving sleep health and supporting recovery.
Study Background
Poor sleep is common among individuals receiving treatment for opioid use disorder, but there are few effective, accessible solutions.
This study aims to develop and test a mobile health (mHealth) behavioral sleep intervention app designed specifically for people receiving medications such as buprenorphine. The app uses evidence-based strategies from behavioral sleep medicine to help participants track and improve their sleep patterns.
By engaging with the app over several weeks, participants will contribute valuable feedback that will help researchers refine and evaluate the program’s effectiveness in improving sleep health and supporting recovery.
Additional Information
This study is being conducted to test whether a smartphone-based behavioral sleep program can help individuals receiving medication-assisted treatment improve their sleep quality.
You may be eligible for this study if you meet the following criteria.
Inclusion Criteria:
- Initiated or modified dose of buprenorphine (suboxone or subutex) treatment in the last 3 months
- Experience poor sleep quality
- Diagnosed with opioid use disorder
- Ages 18+
- Able to read and understand English
- Own an Android or iOS smartphone
- If female, not pregnant
Exclusion Criteria:
- Experiencing psychotic symptoms
If eligible, you will:
Complete a consent appointment and an interview about your sleep and mental health
Use the study app for 6 weeks to complete daily sleep activities and logs
Attend a follow-up appointment after app use
Participants can receive up to $200 for completing all parts of the study.
There is no cost for you to participate in our research study.