在战略接触点使用丁丙诺啡进行阿片类药物使用障碍治疗链接(OUTLAST-B):随机对照试验的原理、设计和演变。

Journal of psychiatry and brain science Pub Date : 2023-01-01 Epub Date: 2023-12-25 DOI:10.20900/jpbs.20230010
Courtney D Nordeck, Anjalee Sharma, Mishka Terplan, Kristi Dusek, Elizabeth Gilliams, Jan Gryczynski
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引用次数: 0

摘要

背景:尽管使用丁丙诺啡治疗阿片类药物使用障碍(OUD)效果显著,且可获得性不断提高,但仍有许多 OUD 患者无法获得治疗服务。本文介绍了一项正在进行的临床试验的基本原理、方法设计、演变和进展,该试验针对的是未接受治疗的阿片类药物使用障碍患者:这项名为 "使用丁丙诺啡在战略接触点进行阿片类药物使用障碍治疗链接"(OUTLAST-B)的研究利用 "战略接触点"(最初是性健康诊所,后来扩展到其他服务场所和参与者的社交网络)进行招募和筛选。未经治疗的 OUD 成人(目标人数 = 360)被随机分配到三个治疗组中的一个:常规护理(UC,加强用药过量教育和纳洛酮发放)、患者指导(PN)或患者指导加丁丙诺啡即时短期过渡处方(PN + BUP)。在 "患者导航 "和 "患者导航 "+"丁丙诺啡 "两组中,"患者导航员 "将与参与者一起工作 2 个月,以帮助他们进入治疗和尽早接受治疗,解决障碍(如身份证、交通),并提供动机支持:主要结果是参加者在 30 天内开始接受 OUD 治疗。对参与者进行基线评估,并在入组后 3 个月和 6 个月对医疗保健利用率、药物使用和一般功能进行跟踪调查。研究还讨论了在 COVID-19 大流行中面临的挑战和招募适应措施:本研究可为如何通过非传统途径接触未经治疗的 OUD 患者并将其与护理联系起来提供启示:该研究已在ClinicalTrials.gov(NCT04991974)上注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Opioid Use Disorder Treatment Linkage at Strategic Touchpoints Using Buprenorphine (OUTLAST-B): Rationale, Design, and Evolution of a Randomized Controlled Trial.

Background: Despite the effectiveness and growing availability of treatment for opioid use disorder (OUD) with buprenorphine, many people with OUD do not access treatment services. This article describes the rationale, methodological design, evolution, and progress of an ongoing clinical trial of treatment linkage strategies for people with untreated OUD.

Methods: The study, titled Opioid Use Disorder Treatment Linkage at Strategic Touchpoints using Buprenorphine (OUTLAST-B), uses "strategic touchpoints", initially sexual health clinics and subsequently broadened to other service venues and participant social networks, for recruitment and screening. Adults with untreated OUD (target N = 360) are randomized to one of the three arms: Usual Care (UC, enhanced with overdose education and naloxone distribution), Patient Navigation (PN), or Patient Navigation with an immediate short-term bridge prescription for buprenorphine (PN + BUP). In the PN and PN + BUP arms, the Patient Navigator works with participants for 2 months to facilitate treatment entry and early retention, resolve barriers (e.g., ID cards, transportation), and provide motivational support.

Results: The primary outcome is OUD treatment entry within 30 days of enrollment. Participants are assessed at baseline and followed at 3- and 6-months post-enrollment on measures of healthcare utilization, substance use, and general functioning. Challenges and recruitment adaptations pursuant to the COVID-19 pandemic are discussed.

Conclusions: This study could provide insights on how to reach people with untreated OUD and link them to care through non-traditional routes.

Trial registration: The study is registered at ClinicalTrials.gov (NCT04991974).

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