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临床试验/NCT07178990
NCT07178990招募中不适用

Mobile Platform for Optimizing Wellness and Engagement in Recovery

University of Michigan1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年12月8日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1
主要终点
Feasibility based on recruitment

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
19 Years 至 63 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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).

排除标准

  • 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.

研究组 & 干预措施

Wellness Condition

Active Comparator

After participants meet eligibility and complete the DynamiCare assessment period, those randomized to this group will receive a wellness digital platform that includes surveys, testing, and tech support.

干预措施: Digital Wellness Arm (Behavioral)

Digital Contingency Management (CM) Intervention Arm

Experimental

After participants meet eligibility and complete the DynamiCare assessment period, participants randomized to this group will receive a comprehensive digital CM platform designed to enhance OAT retention and promote abstinence from alcohol and opioids. This will include the DynamiCare Motivation Support Program.

干预措施: Digital Contingency Management Intervention Arm (Behavioral)

结局指标

主要结局

Feasibility based on recruitment

时间窗: Recruitment period 12 months

Recruitment: ≥60% of participants enrolled

Feasibility based on adherence

时间窗: 6 months (during the Dynamicare program)

Adherence: ≥50% of app-based, biochemically-verified tests completed in the digital CM condition.

Feasibility based on Retention

时间窗: 6 months

Retention: ≥70% of participants retained at 6 months

Acceptability of the intervention

时间窗: 3-month after starting program

Defined as \>70% of participants rating the intervention experience ≥ 4/5 on the Acceptability of Intervention Measure

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lara Coughlin

Associate Professor of Psychiatry

University of Michigan

研究点 (1)

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