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临床试验/NCT04082637
NCT04082637已完成不适用

Mindful Body Awareness Training as an Adjunct to Medication Treatment for Opioid Use Disorder

University of Washington10 个研究点 分布在 1 个国家目标入组 303 人开始时间: 2019年8月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
303
试验地点
10
主要终点
Time Line Follow-back

研究概览

简要总结

The national opioid epidemic requires development of real-world evidence-based treatments for opioid use disorder, including adjuncts to Medication for Opioid Use Disorder (MOUD). Interventions are needed that address the complex needs of patients with opioid use disorder, which include substantial mental health co-morbidity and high rates of chronic pain related to the complex interaction of opioid prescribing for pain and opioid use disorder. This study leverages recent federal and state opioid use disorder treatment initiatives as a platform for testing a promising mind-body intervention, Mindful Awareness in Body-oriented Therapy (MABT) as an adjunct to MOUD in multiple clinical settings funded primarily through the Washington Opioid State Targeted Response (STR) program. MABT, a novel mindfulness-based intervention, uniquely addresses aspects of awareness, interoception, and regulation that may be associated with pain, mental health distress, and behavioral control that increase risk of relapse and poor treatment outcomes. Using a randomized, two-group, repeated measures design, we will compare those who receive MABT+ MOUD vs. MOUD only. The overarching goal of this application is to test MABT to improve MOUD health outcomes. The specific aims for the combined R33/R01 clinical protocol are to: 1) evaluate the effectiveness of MABT + TAU (MOUD) compared to TAU only in reducing opioid use and other substances; 2) examine the effectiveness of MABT + TAU to improve mental and physical health vs. TAU only; 3) examine the effectiveness of MABT + TAU to positively affect substance use related outcomes of craving and treatment retention vs. TAU only. For the R01, there is an additional aim to explore the effectiveness of additional MABT dose offered at 6 months to those with continued substance use (non-responders) compared to those with continued substance use at 6 months in TAU. A two-group (n = 165/165), randomized controlled repeated measures design will be employed. Three hundred thirty individuals engaged in MOUD will be recruited for participation at outpatient treatment sites. Assessments will be administered at baseline, post-intervention (3 months from baseline), and at 6, 9, and 12 months. Results of this study will inform the evidence base for behavioral treatment adjuncts to MOUD and directly impact the future direction of the Washington Opioid STR program.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • diagnosed with opioid use disorder
  • enrolled in a medication treatment program for opioid use disorder
  • is stable in program involving, (if on buprenorphine) Rx appointments less frequent than once/week; (if on methadone) at least 90 days in treatment with a minimum dose of 60mg, no missed dose evaluation appointments in past 30 days, and no more than 3 missed doses in 30 days
  • willing to forego (non-study) manual (e.g., massage) and/or mind-body therapies (e.g., mindfulness meditation) for 3 months
  • willing to sign release for access of electronic medical records
  • fluent in English
  • able to attend study sessions when offered

排除标准

  • unwilling or unable to remain in MT treatment for the duration of the trial (includes planned relocation, pending incarceration, planned surgical procedures, etc.)
  • over 24 weeks gestation or unknown gestation, if pregnant
  • reports, or is noted by clinical or study staff as showing, overt psychosis or other conditions such as cognitive impairment

研究组 & 干预措施

MABT* + Medication Treatment

Experimental

Mindful Awareness in Body-oriented Therapy + Medication Treatment

干预措施: Mindful Awareness in Body-oriented Therapy (Behavioral)

Treatment as Usual

No Intervention

Treatment as Usual is medication for the treatment of opioid use disorder

结局指标

主要结局

Time Line Follow-back

时间窗: 90 days

Patient-reported days of opioid use and other substances

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

Cynthia Price

Research Professor

University of Washington

研究点 (10)

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