Mobile Platform for Optimizing Wellness and Engagement in Recovery (NCT07178990) | Clinical Trial Compass
RecruitingNot Applicable
Mobile Platform for Optimizing Wellness and Engagement in Recovery
United States50 participantsStarted 2025-12-08
Plain-language summary
This pilot study addresses the urgent public health crisis of co-occurring opioid and alcohol use disorders (OUD-AUD), leading causes of mortality in the United States, by testing a scalable digital contingency management (CM) treatment among Medicaid beneficiaries. The study aims to evaluate the feasibility and acceptability of digital CM for OUD-AUD recovery, while also planning for broader implementation.
Who can participate
Age range
19 Years – 63 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Participants must be enrolled in the Michigan Medicaid program
* Opioid agonist treatment (OAT): Participants must have initiated OAT with buprenorphine or methadone
* Participants must have an OAT prescription and Alcohol use disorder (AUD) based on self-report measure during screening
* Participants must have regular access to a working smartphone and internet connection.
* Participants must have a reliable mailing address to receive study supplies (e.g., salivary drug tests).
Exclusion Criteria:
* Primary Medicare Coverage: Individuals that are dual-eligible for Medicaid and Medicare and aged 65 or older, due to limited availability of Medicaid claims data for this group
* Individuals that cannot voluntarily provide informed consent themselves for any reason, including legal incompetency
* Individuals with substantial cognitive impairment that would interfere with study participation
* Individuals unable to read or understand English
* Individuals experiencing active suicidality or psychosis.
* Individuals with a planned admission to residential treatment or incarceration during the study period.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Feasibility based on recruitment
Timeframe: Recruitment period 12 months
2
Feasibility based on adherence
Timeframe: 6 months (during the Dynamicare program)