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一项随机对照试验的方案,采用递进式护理方法,为有物质使用障碍的跨性别女性和性少数男性提供 PrEP 导航,同时使用和不使用意外管理:援助服务知识-PreP(A.S.K.-PreP)。

Protocol for a randomized controlled trial with a stepped care approach, utilizing PrEP navigation with and without contingency management, for transgender women and sexual minority men with a substance use disorder: Assistance Services Knowledge-PrEP (A.S.K.-PrEP).

机构信息

Friends Research Institute, Inc, Los Angeles, CA, USA.

Center for HIV Identification, Prevention and Treatment Services, Department of Family Medicine, University of California, Los Angeles, Los Angeles, CA, USA.

出版信息

Addict Sci Clin Pract. 2024 Nov 9;19(1):79. doi: 10.1186/s13722-024-00482-6.

Abstract

BACKGROUND

In the United States, most (~ 70%) annual newly diagnosed HIV infections are among substance-using sexual minority men (SMM) and gender minority transgender women (trans women). Trans women and SMM are more likely to report or be diagnosed with a substance use disorder (SUD) than their cisgender or heterosexual counterparts and the presence of an SUD substantially increases the risk of HIV infection in both groups. Although Pre-Exposure Prophylaxis (PrEP) is highly effective, initiation, adherence, and persistence are exclusively behavioral outcomes; thus, the biomedical benefits of PrEP are abrogated by substance use. SUD is also associated with reduced quality-of-life, and increased overdose deaths, utilization of high-cost healthcare services, engagement in a street economy, and cycles of incarceration.

OBJECTIVE

To determine the optimal (considering efficacy and cost-effectiveness) strategy for advancement along the PrEP Care Continuum among trans women and SMM with an SUD.

METHODS

This study will implement a randomized controlled trial, evaluating two Stepped Care approaches involving A.S.K.-PrEP vs. standard of care (SOC) to determine optimal intervention strategies for trans women and SMM with an SUD (N = 250; n = 83 trans women; n = 167 SMM) for advancement along the PrEP Care Continuum. Participants will be randomized (3:1) to Stepped Care (n = 187) or SOC (n = 63). Participants in the Stepped Care arm will be assessed at 3-months for intervention response; responders will be maintained in A.S.K.-PrEP, while non-responders will receive added attention to their SUD via Contingency Management (CM). Non-responders will be re-randomized (1:1) to either (a) receive A.S.K.-PrEP + CM, or (b) shift the primary focus to their SUD (CM alone).

RESULTS

Recruitment and enrollment began in May 2023. Recruitment will span approximately 36 months. Data collection, including all follow-up assessments, is expected to be completed in April 2027.

DISCUSSION

Trans women and SMM with an SUD have the two highest HIV prevalence rates in the United States, which underscores the urgent need for effective measures to develop scalable behavioral interventions that can encourage advancement along the PrEP Care Continuum. To improve public health, researchers must identify scalable and cost-effective behavioral interventions to promote PrEP initiation, adherence, and persistence among trans women and SMM who use substances.

TRIAL REGISTRATION

This trial has been registered at ClinicalTrials.gov under the number NCT05934877.

摘要

背景

在美国,大多数(约 70%)新诊断的艾滋病病毒感染发生在使用药物的性少数男性(SMM)和性别少数跨性别女性(跨性别女性)中。跨性别女性和 SMM 比他们的顺性别或异性恋者更有可能报告或被诊断为药物使用障碍(SUD),并且 SUD 的存在会大大增加这两个群体感染艾滋病病毒的风险。尽管暴露前预防(PrEP)非常有效,但启动、坚持和持续使用都是行为结果;因此,药物使用会削弱 PrEP 的生物医学益处。SUD 还与生活质量下降、过量死亡增加、高成本医疗保健服务的利用、参与街头经济以及监禁循环有关。

目的

确定具有 SUD 的跨性别女性和 SMM 沿着 PrEP 护理连续体前进的最佳(考虑疗效和成本效益)策略。

方法

本研究将实施一项随机对照试验,评估两种逐步护理方法,即 A.S.K.-PrEP 与标准护理(SOC),以确定具有 SUD 的跨性别女性和 SMM 沿着 PrEP 护理连续体前进的最佳干预策略(N=250;n=83 名跨性别女性;n=167 名 SMM)。参与者将以 3:1 的比例随机分配到逐步护理组(n=187)或 SOC 组(n=63)。逐步护理组的参与者将在 3 个月时接受干预反应评估;反应者将继续接受 A.S.K.-PrEP,而无反应者将通过条件管理(CM)接受更多的 SUD 关注。无反应者将重新随机(1:1)分配到以下两种情况之一:(a)接受 A.S.K.-PrEP+CM,或(b)将主要重点转移到他们的 SUD(单独 CM)。

结果

招募和入组于 2023 年 5 月开始。预计招募将持续约 36 个月。数据收集,包括所有随访评估,预计将于 2027 年 4 月完成。

讨论

具有 SUD 的跨性别女性和 SMM 的 HIV 感染率在美国是最高的,这突显了迫切需要采取有效的措施来开发可扩展的行为干预措施,以鼓励他们沿着 PrEP 护理连续体前进。为了改善公共卫生,研究人员必须确定可扩展且具有成本效益的行为干预措施,以促进使用药物的跨性别女性和 SMM 启动、坚持和持续使用 PrEP。

试验注册

这项试验已在 ClinicalTrials.gov 注册,编号为 NCT05934877。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ae7/11549772/78c97706c588/13722_2024_482_Figa_HTML.jpg

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