跳至主要内容
临床试验/NCT07780097
NCT07780097Enrolling By Invitation不适用

A Pilot Randomized Controlled Trial to Improve Outpatient Initiation of Medication for Opioid Use Disorder (MOUD) Following Hospitalization: The TRTME (Tailored Overdose Risk Feedback, Testimonials for MOUD Treatment, and Education on MOUD and Opioid Overdose) Trial

T. John Winhusen, PhD2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年8月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
30
试验地点
2
主要终点
Outpatient MOUD initiation

研究概览

简要总结

The primary objective of this study is to evaluate the ability of TRTME to increase initiation of MOUD outpatient treatment and MOUD knowledge in hospitalized patients with OUD deemed to be good candidates for MOUD by the UCMC Addiction Consult Team (ACT). The secondary objective is to evaluate the ability of TRTME to decrease stigma and increase drug self-efficacy.

详细描述

This is an intent-to-treat, two-arm, open-label, pragmatic randomized controlled trial. Eligible participants will be randomized in a 1:1 ratio to TRTME or Control. Participants will receive the assigned intervention following randomization, will complete a post-assessment following treatment receipt, and will complete a follow-up phone call at approximately one month posthospital discharge.

All participants will complete assessments of their opioid-overdose and MOUD knowledge and their risk for experiencing an opioid-overdose during baseline. TRTME participants will be offered a 15-minute intervention in which a trained research staff member reviews personal feedback reports with the recipient to provide information on: 1) the items missed on the knowledge assessment; and 2) their personal overdose risk factors. TRTME participants will also have the opportunity to view short videos from patients talking about their experiences with methadone or buprenorphine treatment. Control participants will be offered two SAMHSA handouts.

Enrollment is expected to take place over a period of approximately 7.5 months. Duration of study participation will be approximately 5 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
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
否

入选标准

  • •18 years of age or older;
  • •A good candidate for methadone or buprenorphine treatment according to a member of the UCMC Addiction Consult Team

排除标准

  • •Have a current planned discharge to a nursing facility
  • •be currently in jail, prison, or any inpatient overnight facility as required by court of law or have pending legal action with high probability of incarceration or court-mandated inpatient treatment
  • •Unable to demonstrate adequate understanding of study procedures during the consent process

研究组 & 干预措施

Control

No Intervention

Control participants will be offered two SAMHSA handouts: 1) "Opioid Overdose Prevention Toolkit: Safety Advice for Patients and Family Members"; and 2) "Medication-Assisted Treatment for Opioid Addiction: Facts for Families and Friends". These handouts can be offered as physical copies or electronically.

TRTME

Experimental

TRTME participants will be offered a 15-minute intervention in which a trained research staff member reviews personal feedback reports with the recipient to provide information on: 1) the items missed on the knowledge assessment; and 2) their personal overdose risk factors. TRTME participants will also have the opportunity to view short videos from patients talking about their experiences with methadone or buprenorphine treatment.

干预措施: TRTME (Behavioral)

结局指标

主要结局

Outpatient MOUD initiation

时间窗: 30 days

The primary outcome is verified enrollment in outpatient MOUD within 30 days post-discharge. Participants will be asked about their enrollment in MOUD approximately 30 days after their discharge from the hospital. Participants reporting having enrolled in treatment will be asked to provide a release of information for the treatment program to verify date of treatment enrollment.

次要结局

  • MOUD knowledge score(Immediately after the intervention)
  • MOUD Stigma(Immediately after the intervention)
  • Drug Self-efficacy(Immediately after the intervention)
  • Opioid-overdose knowledge score(Immediately after the intervention)

研究者

发起方
T. John Winhusen, PhD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

T. John Winhusen, PhD

Professor; Vice Chair and Division Director of Addiction Sciences

University of Cincinnati

研究点 (2)

Loading locations...

相似试验