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临床试验/NCT04712981
NCT04712981进行中(未招募)不适用

Adapting the HOPE Online Support Intervention to Increase MAT Uptake Among OUD Patients

University of California, Irvine1 个研究点 分布在 1 个国家目标入组 640 人开始时间: 2021年4月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
640
试验地点
1
主要终点
Number of requests to receive a resource on medications that can be used to treat opioid use disorder

研究概览

简要总结

In a randomized controlled trial, with 3, 6-month and 1-year follow-up, this application aims to explore whether and how the HOPE intervention can be adapted to increase MOUD uptake among OUD patients, assess the effectiveness of using HOPE to increase MOUD requests, and analyze online community data to improve future intervention implementation and sustainability.

详细描述

The proposed study is a low-risk, randomized control trial to assess the efficacy of the HOPE (Harnessing Online Peer Education) intervention, an evidenced-based peer-led social media/online community intervention (e.g., Facebook Groups), to increase self-reported requests for medications for opioid use disorder (MOUD) among patients with moderate to severe opioid use disorder (OUD). Participants will be recruited using a variety of recruitment methods including social media sites (e.g., Facebook), referral by physicians, medical records, research study websites (e.g., UCIMC Clinical Trials website), and study flyers disseminated at various venues, including clinics, group meetings, and shelters. Once enrolled, participants will be randomly assigned to an intervention or control group. Intervention group participants will be invited to join a private and hidden (unable to be viewed or searched for by others) group on Facebook, with approximately 6 peer leaders included in the group. Those in the control group will be invited into a Facebook group, but without peer leaders. The intervention will last 12 weeks. Study measures will be collected at the beginning of the study (baseline), after the completion of the intervention (3 months), with follow up surveys at 6 and 12 months after the study. Participants will be recruited in 5 waves, 2 waves of rural residents and 3 waves of urban residents.

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 (Participant)

入排标准

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

入选标准

  • •≥ 18 years of age;
  • •Resident of CA, NV, AZ, OR, WA;
  • •English speakers only;
  • •Has moderate to severe OUD;
  • •Is not currently prescribed MOUD;
  • •Reports using social media at least 2x per week;
  • •Has, or is willing to create a Facebook/social media account and accept a friend request and group invite from our study social media page

排除标准

  • •Anyone who does not fit inclusion criteria above
  • •Was a participant in phase I of the study
  • •Participants with active, unstable opioid, alcohol, sedative, or other substance use and/or unstable medical or psychiatric conditions as assessed by the study questionnaires will be reviewed by the study physician consultants and will be excluded and referred for acute care including detoxification, if needed.

研究组 & 干预措施

Intervention

Experimental

HOPE intervention peer-led online community

干预措施: HOPE (Behavioral)

Control

No Intervention

Online community without HOPE intervention psychological components

结局指标

主要结局

Number of requests to receive a resource on medications that can be used to treat opioid use disorder

时间窗: request during the course of the 12-week community

Participants will be invited to request an informational resource on medications for opioid use disorder as well as to ask for assistance scheduling an appointment with a provider on this topic. We will count the number of participants making this request

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

Sean D Young

Professor

University of California, Irvine

研究点 (1)

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