跳至主要内容
临床试验/NCT05817825
NCT05817825招募中不适用

Pilot Testing a Novel Remotely Delivered Intensive Outpatient Program for Individuals With Opioid Use Disorder Hospitalized With Serious Injection-related Infection

Brigham and Women's Hospital2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年11月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
2
主要终点
Feasibility of the intervention program

研究概览

简要总结

This study aims to test a remotely delivered IOP program ("SmartIOP") for OUD patients who are hospitalized for serious injection-related infections. This will be a pilot trial to assess the feasibility of the IOP program and examine OUD-related outcomes following discharge from the hospital.

详细描述

The aim is to conduct a single-arm pilot study of 20 participants who are hospitalized for serious injection-related infections to complete the newly tailored program. The intervention to be developed and tested has two components: 1) the remotely delivered IOP ("Smart IOP"), and 2) a peer recovery coach who will provide support and accountability to the participant. The feasibility of the intervention will be established by evaluating recruitment and the acceptability of the program according to a priori benchmarks. The study team will assess the program's preliminary efficacy by evaluating OUD-related outcomes for up to 28 days after discharge from the hospital. The study will be conducted at Brigham and Women's Hospital (BWH), an urban, 793-bed academic medical center located in Boston, MA, and a major teaching hospital for Harvard Medical School.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • English-speaking adults aged 18 and above
  • Any DSM-5 substance use disorder
  • Can identify at least 2 individuals who can act as points of contact following discharge from the hospital

排除标准

  • Psychotic disorder, active suicidality, or homicidally
  • Condition likely to be terminal during the study period
  • Unable to perform consent due to impaired mental status

结局指标

主要结局

Feasibility of the intervention program

时间窗: Immediately Post Intervention

We expect the results to demonstrate adequate feasibility, as defined by exceeding the threshold for adequate recruitment feasibility and good program acceptability. Adequate recruitment feasibility is defined as enrolling more than 70% of those eligible individuals. Excellent program acceptability is defined as \>70% of the participants complete at least 70% of the Smart IOP intervention, and good program acceptability if \>60% of participants did.

次要结局

  • Retention with MOUD treatment(7-day Follow Up, 14-day Follow Up, 21-day Follow Up, and 28-Day Follow Up)
  • Illicit opioid use(7-day Follow Up, 14-day Follow Up, 21-day Follow Up, and 28-Day Follow Up)

研究者

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

Joji Suzuki, MD

Director, Division of Addiction Psychiatry

Brigham and Women's Hospital

研究点 (2)

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