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临床试验/NCT07778394
NCT07778394招募中不适用

The Vira Platform: A Contextually Triggered Just-in-Time Adaptive Intervention for Opioid Use Disorder

Rhode Island Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年8月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Medication for Opioid Use Disorder Retention

研究概览

简要总结

Many patients stop medication-based treatments for Opioid Use Disorder (OUD) prematurely, placing them at increased risk for overdose and death. Providing targeted interventions for OUD, particularly through an accessible, digital health platform, is a potential way to enhance recovery and keep patients engaged in care. The current study seeks to test whether a digital mental health platform, delivered by peer recovery support specialists to individuals prescribed buprenorphine or methadone medication, will improve treatment outcomes for this high risk population.

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Current Opioid Use Disorder diagnosis
  • Prescribed buprenorphine or methadone
  • Initiated or reinitiated buprenorphine or methadone treatment recently
  • Access to personal smartphone

排除标准

  • Not fluent in English
  • Limited mental capacity or inability to provided informed consent

研究组 & 干预措施

Vira Path

Experimental

干预措施: Treatment-As-Usual (Behavioral)

Treatment-as-Usual

Active Comparator

干预措施: Treatment-As-Usual (Behavioral)

Vira Path

Experimental

干预措施: Vira Platform (Behavioral)

结局指标

主要结局

Medication for Opioid Use Disorder Retention

时间窗: Baseline & 3-Month Follow-up

Retention on buprenorphine or methadone treatment will be verified through medical record chart review.

Substance Use Disorder Treatment Engagement

时间窗: Baseline & 3-Month Follow-up

Addiction treatment records as assessed through medical records will be assessed for participation in addiction treatment services (e.g., 'detox', inpatient services, outpatient therapy).

次要结局

  • Opioid Use assessed with the Timeline Follow-back(Baseline & 3-Month Follow-up)
  • Anhedonia assessed with the Snaith-Hamilton Pleasure Scale(Baseline & 3-Month Follow-up)
  • Sleep Deficiency assessed with the Insomnia Severity Index (ISI)(Baseline & 3-Month Follow-up)
  • Negative Affect assessed with the Positive Affect and Negative Affect Schedule-Expanded Form(Baseline & 3-Month Follow-up)
  • Perceived Quality of Life Measured with the Quality of Life Enjoyment and Satisfaction Questionnaire-Short Form(Baseline & 3-Month Follow-up)
  • Wellbeing measured by the World Health Organization-Five Well-Being Index(Baseline & 3-Month Follow-up)
  • Perceived Social Support assessed with the Multidimensional Scale of Perceived Social Support(Baseline & 3-Month Follow-up)
  • Participant Safety(Baseline & 3-Month Follow-up)
  • Opioid Craving measured with the Opioid Craving Scale(Baseline & 3-Month Follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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