Machine Learning + Peer Support for Substance Use Disorder
Trial Summary
What is the purpose of this trial?
The goal of this clinical trial is to study the relationship between substance cravings, cognitive performance, behaviors, and physiological markers in individuals with substance use disorder, as well as the effects of peer recovery intervention in response to abnormal biomarker data detected by wearable technology (e.g., Oura ring, smart watch) and participant responses to questionnaires and cognitive tasks completed on the RNI Health application.
Do I need to stop my current medications for the trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What data supports the effectiveness of the treatment PRSS, Peer Recovery Support, PRSS Intervention for Substance Use Disorder?
Research suggests that peer recovery support services (PRSS) can help reduce substance use and relapse rates, improve relationships with treatment providers, and increase treatment satisfaction for individuals with substance use disorder. However, more rigorous studies are needed to confirm these benefits and understand how best to implement PRSS.12345
Is the Machine Learning + Peer Support for Substance Use Disorder treatment safe for humans?
How does the Machine Learning + Peer Support treatment for Substance Use Disorder differ from other treatments?
This treatment is unique because it combines machine learning algorithms, which predict stress and drug cravings using data like GPS, with peer support, where individuals with similar experiences provide nonprofessional assistance. This approach aims to deliver timely interventions and support, unlike traditional treatments that may not use real-time data or peer involvement.3591011
Research Team
James J Mahoney, Ph.D.
Principal Investigator
West Virginia University Rockefeller Neuroscience Institute
Eligibility Criteria
This trial is for adults over 18 with substance use disorders who are currently or were previously treated at a WVU Medicine Clinic, or residents of sober living facilities. Participants must be able to consent and download the required health app and wearable device apps on their smart devices.Inclusion Criteria
Exclusion Criteria
Trial Timeline
Screening
Participants are screened for eligibility to participate in the trial
Initial Monitoring
Participants are monitored for 3 months to collect baseline data using wearable technology and the RNI Health app
Randomization and Intervention
Participants are randomized to either standard-of-care treatment or PRSS intervention, with continuous monitoring and periodic assessments
Follow-up
Participants are monitored for safety and effectiveness after intervention
Treatment Details
Interventions
- PRSS (Behavioural Intervention)
Find a Clinic Near You
Who Is Running the Clinical Trial?
West Virginia University
Lead Sponsor
Dr. William P. Petros
West Virginia University
Chief Medical Officer
PharmD from West Virginia University
Dr. Clay B. Marsh
West Virginia University
Chief Executive Officer since 2015
MD from West Virginia University, Bachelor’s in Biology from West Virginia University