跳至主要内容
临床试验/NCT07362082
NCT07362082尚未招募不适用

A Randomized Clinical Trial of Telehealth Treatment for Opioid Use Disorders

Yale University1 个研究点 分布在 1 个国家目标入组 470 人开始时间: 2026年8月15日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
470
试验地点
1
主要终点
Mean time to first buprenorphine prescription

研究概览

简要总结

This trial will assess effects of enrollment in a comprehensive telehealth platform, RecoveryPad (RP), in adults with moderate or severe opioid use disorder.

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

入选标准

  • Can speak, read and write in English
  • Provision of signed and dated informed consent form
  • Screened positive for OUD, moderate or severe, based on the Diagnostic and Statistical Manual-5th Edition
  • Have a working cell phone number and working device that can access a web browser and receive texts (i.e., smartphone, tablet or computer)
  • Can provide a working email address OR be willing to create one

排除标准

  • Current use of buprenorphine, methadone, or naltrexone for a substance use disorder
  • Pregnancy
  • Known current suicide risk based on participant self-report
  • On parole or incarcerated at time of enrollment based on participant self-report

研究组 & 干预措施

Treatment as usual

No Intervention

Treatment as usual: referrals to harm reduction and other community resources that are already being given to individuals in the various community and healthcare settings from which these participants are being recruited.

RecoveryPad platform

Experimental

Participants randomized to RecoveryPad platform

干预措施: RecoveryPad platform (Device)

结局指标

主要结局

Mean time to first buprenorphine prescription

时间窗: 30 days post enrollment

Mean time to first buprenorphine prescription within 30 days of engagement with RP.

次要结局

  • Number of participants with current MOUD prescription(90 days post enrollment)
  • Mean number overdose events(30 and 90 days post enrollment)
  • Number of participants with methadone referral and induction(90 days post enrollment)

研究者

发起方
Yale University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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