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一项基于理论的芬太尼过量教育和芬太尼检测条分发干预以降低阿片类药物过量率的随机临床试验:一项随机对照试验的研究方案。

A randomized clinical trial of a theory-based fentanyl overdose education and fentanyl test strip distribution intervention to reduce rates of opioid overdose: study protocol for a randomized controlled trial.

机构信息

Department of Epidemiology, Brown University School of Public Health, Providence, Rhode Island, USA.

Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.

出版信息

Trials. 2020 Nov 26;21(1):976. doi: 10.1186/s13063-020-04898-8.

Abstract

BACKGROUND

Opioid overdose deaths involving synthetic opioids, particularly illicitly manufactured fentanyl, remain a substantial public health concern in North America. Responses to overdose events (e.g., administration of naloxone and rescue breathing) are effective at reducing mortality; however, more interventions are needed to prevent overdoses involving illicitly manufactured fentanyl. This study protocol aims to evaluate the effectiveness of a behavior change intervention that incorporates individual counseling, practical training in fentanyl test strip use, and distribution of fentanyl test strips for take-home use among people who use drugs.

METHODS

Residents of Rhode Island aged 18-65 years who report recent substance use (including prescription pills obtained from the street; heroin, powder cocaine, crack cocaine, methamphetamine; or any drug by injection) (n = 500) will be recruited through advertisements and targeted street-based outreach into a two-arm randomized clinical trial with 12 months of post-randomization follow-up. Eligible participants will be randomized (1:1) to receive either the RAPIDS intervention (i.e., fentanyl-specific overdose education, behavior change motivational interviewing (MI) sessions focused on using fentanyl test strips to reduce overdose risk, fentanyl test strip training, and distribution of fentanyl test strips for personal use) or standard overdose education as control. Participants will attend MI booster sessions (intervention) or attention-matched control sessions at 1, 2, and 3 months post-randomization. All participants will be offered naloxone at enrolment. The primary outcome is a composite measure of self-reported overdose in the previous month at 6- and/or 12-month follow-up visit. Secondary outcome measures include administratively linked data regarding fatal (post-mortem investigation) and non-fatal (hospitalization or emergency medical service utilization) overdoses.

DISCUSSION

If the RAPIDS intervention is found to be effective, its brief MI and fentanyl test strip training components could be easily incorporated into existing community-based overdose prevention programming to help reduce the rates of fentanyl-related opioid overdose.

TRIAL REGISTRATION

ClinicalTrials.gov NCT04372238 . Registered on 01 May 2020.

摘要

背景

涉及合成阿片类药物,特别是非法制造的芬太尼的阿片类药物过量死亡仍然是北美地区的一个重大公共卫生问题。对过量事件的反应(例如,给予纳洛酮和抢救呼吸)可有效降低死亡率;然而,需要更多的干预措施来预防涉及非法制造的芬太尼的过量用药。本研究方案旨在评估一种行为改变干预措施的有效性,该措施包括个体咨询、芬太尼检测条使用的实际培训以及向吸毒者分发芬太尼检测条以便带回家使用。

方法

罗德岛州年龄在 18-65 岁之间、报告最近有药物使用(包括从街头获取的处方药丸;海洛因、粉末可卡因、可卡因、冰毒;或任何注射药物)的居民(n=500)将通过广告和有针对性的街头外展招募到一项为期 12 个月的随机临床试验中,在随机分组后进行 12 个月的随访。符合条件的参与者将被随机分为 1:1 组,分别接受 RAPIDS 干预(即,芬太尼特异性过量教育、行为改变动机访谈(MI)课程,重点是使用芬太尼检测条降低过量风险、芬太尼检测条培训以及个人使用的芬太尼检测条分发)或标准过量教育作为对照组。参与者将在随机分组后 1、2 和 3 个月接受 MI 强化课程(干预组)或注意力匹配的对照组课程。所有参与者在入组时都将获得纳洛酮。主要结局是在 6 个月和/或 12 个月随访时报告的前一个月自我报告的过量用药的综合指标。次要结局指标包括行政链接数据,涉及致命(尸检调查)和非致命(住院或紧急医疗服务利用)过量用药。

讨论

如果 RAPIDS 干预被证明有效,其简短的 MI 和芬太尼检测条培训内容可以很容易地纳入现有的基于社区的过量预防方案中,以帮助降低与芬太尼相关的阿片类药物过量用药的发生率。

试验注册

ClinicalTrials.gov NCT04372238。于 2020 年 5 月 1 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/748e/7690169/2192edd4608c/13063_2020_4898_Fig1_HTML.jpg

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