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同伴干预将过量幸存者与治疗联系起来 (PILOT):在国家药物滥用研究所临床试验网络内进行的多地点、随机对照试验的方案。

Peer Intervention to Link Overdose Survivors to Treatment (PILOT): Protocol for a Multisite, Randomized Controlled Trial Conducted Within the National Institute on Drug Abuse Clinical Trials Network.

机构信息

Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, United States.

Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, United States.

出版信息

JMIR Res Protoc. 2024 Sep 17;13:e60277. doi: 10.2196/60277.

Abstract

BACKGROUND

The increase in opioid-related overdoses has caused a decrease in average life expectancy, highlighting the need for effective interventions to reduce overdose risk and prevent subsequent overdoses. Peer support specialists (PSSs) offer an appealing strategy to engage overdose survivors and reduce overdose risk, but randomized controlled trials are needed to formalize peer-led interventions and evaluate their effectiveness.

OBJECTIVE

This National Institute on Drug Abuse Clinical Trials Network (CTN) study is a multisite, prospective, pilot randomized (1:1) controlled trial (CTN protocol 0107) that aims to evaluate the effectiveness of an emergency department (ED)-initiated, peer-delivered intervention tailored for opioid overdose survivors (Peer Intervention to Link Overdose survivors to Treatment [PILOT]), compared with treatment as usual (TAU).

METHODS

This study evaluates the effectiveness of the 6-month, PSS-led PILOT intervention compared with TAU on the primary outcome of reducing overdose risk behavior 6 months after enrollment. Adults (aged ≥18 years; N=150) with a recent opioid-related overdose were identified and approached in the ED. Participants were screened and enrolled, either in the ED or within 7 days of ED discharge at research offices or in the community and then asked to complete study visits at months 1, 3, 6 (end of intervention), and 7 (follow-up). Participants were enrolled at 3 study sites in the United States: Greenville, South Carolina; Youngstown, Ohio; and Everett, Washington. Participants randomized to the PILOT intervention received a 6-month, PSS-led intervention tailored to each participant's goals to reduce their overdose risk behavior (eg, overdose harm reduction, housing, medical, and substance use treatment or recovery goals). Participants randomized to TAU received standard-of-care overdose materials, education, and services provided through the participating EDs. This paper describes the study protocol and procedures, explains the design and inclusion and exclusion decisions, and provides details of the peer-led PILOT intervention and supervision of PILOT PSSs.

RESULTS

Study enrollment opened in December 2021 and was closed in July 2023. A total of 150 participants across 3 sites were enrolled in the study, meeting the proposed sample size for the trial. Primary and secondary analyses are underway and expected to be published in early 2025.

CONCLUSIONS

There is an urgent need to better understand the characteristics of overdose survivors presenting to the ED and for rigorous trials evaluating the effectiveness of PSS-led interventions on engaging overdose survivors and reducing overdose risk. Results from this pilot randomized controlled trial will provide a description of the characteristics of overdose survivors presenting to the ED; outline the implementation of PSS services research in ED settings, including PSS implementation of PSS supervision and activity tracking; and inform ED-initiated PSS-led overdose risk reduction interventions and future research to better understand the implementation and efficacy of these interventions.

TRIAL REGISTRATION

ClinicalTrials.gov NCT05123027; https://clinicaltrials.gov/study/NCT05123027.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/60277.

摘要

背景

阿片类药物相关过量的增加导致平均预期寿命下降,这凸显了需要采取有效干预措施来降低过量风险并预防后续过量的必要性。同伴支持专家(PSS)为接触过量幸存者并降低过量风险提供了一种有吸引力的策略,但需要随机对照试验来规范同伴主导的干预措施并评估其效果。

目的

本国家药物滥用研究所临床试验网络(CTN)研究是一项多地点、前瞻性、试点随机(1:1)对照试验(CTN 方案 0107),旨在评估针对阿片类药物过量幸存者的由急诊室(ED)启动、由同伴提供的干预措施(同伴干预以将过量幸存者与治疗联系起来 [PILOT])的有效性,与常规治疗(TAU)相比。

方法

本研究评估了 6 个月、由 PSS 主导的 PILOT 干预措施与 TAU 相比,在招募后 6 个月降低过量风险行为的主要结局方面的有效性。在 ED 中识别并接近最近发生阿片类药物相关过量的成年人(年龄≥18 岁;N=150)。对参与者进行筛查和入组,要么在 ED 中,要么在 ED 出院后 7 天内在研究办公室或社区进行,然后要求他们在第 1、3、6 个月(干预结束)和第 7 个月(随访)进行研究访问。参与者在美国的 3 个研究地点入组:南卡罗来纳州的格林维尔、俄亥俄州的扬斯敦和华盛顿州的埃弗雷特。随机分配至 PILOT 干预组的参与者接受了为期 6 个月的、针对每个参与者目标的由 PSS 主导的干预措施,以降低他们的过量风险行为(例如,减少过量伤害、住房、医疗和物质使用治疗或康复目标)。随机分配至 TAU 的参与者接受了通过参与的 ED 提供的标准过量材料、教育和服务。本文描述了研究方案和程序,解释了设计和纳入排除决策,并提供了同伴主导的 PILOT 干预措施和 PILOT PSS 监督的详细信息。

结果

研究于 2021 年 12 月开放入组,2023 年 7 月关闭。3 个地点共入组了 150 名参与者,达到了试验的预期样本量。正在进行主要和次要分析,预计将于 2025 年初公布结果。

结论

目前迫切需要更好地了解到 ED 就诊的过量幸存者的特征,需要进行严格的试验来评估 PSS 主导的干预措施在接触过量幸存者和降低过量风险方面的有效性。这项试点随机对照试验的结果将提供 ED 就诊过量幸存者特征的描述;概述 ED 环境中 PSS 服务研究的实施情况,包括 PSS 对 PSS 监督和活动跟踪的实施情况;并为 ED 发起的 PSS 主导的降低过量风险干预措施和未来研究提供信息,以更好地了解这些干预措施的实施和效果。

试验注册

ClinicalTrials.gov NCT05123027;https://clinicaltrials.gov/study/NCT05123027。

国际注册报告标识符(IRRID):DERR1-10.2196/60277。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed90/11445628/a00b6fcfee41/resprot_v13i1e60277_fig1.jpg

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