University of Texas Health Science Center at Houston, Houston, USA.
Department of Emergency Medicine, University of Texas Health Science Center at Houston, Houston, USA.
BMC Infect Dis. 2023 Jan 27;23(1):57. doi: 10.1186/s12879-023-08019-z.
Cisgender (cis) Black women in the USA are more likely to become HIV positive during their lifetime than other women. We developed and implemented a behavioral intervention, Increasing PrEP (iPrEP), the first pilot randomized controlled trial (RCT) aimed at motivating cis Black women to be willing to use PrEP for HIV prevention and attend an initial PrEP clinic visit following an emergency department visit.
Eligible participants were Black cisgender women ages 18-55 years who acknowledged recent condomless sex and substance use. Participants were randomized to iPrEP or usual care (UC). iPrEP is a survey-based intervention designed to raise awareness and knowledge about PrEP. Participants completed an assessment of knowledge of and willingness to use PrEP before and after the intervention, then received a warm-hand off with referral to a local PrEP clinic. Enrolled participants were followed for 6 months.
Forty enrolled participants were ages 18-54 years. Education levels varied evenly between some high school education and graduate education. Most participants were single (n = 25) or married (n = 7). Twenty-two participants were employed full-time. Pre-test results indicated that 21 of 40 participants had heard of PrEP. All participants identified PrEP as a daily HIV prevention medication. For those randomized to iPrEP, the odds of knowing about PrEP at post-test, when controlling for baseline, were higher relative to UC (OR = 5.22, 95%CrI = 0.50, 94.1]. iPrEP did not have any effect on willingness relative to UC. The estimate for iPrEP on willingness is marginally higher (4.16 vs. 4.04; i.e., 0.12 points higher); however, the posterior probability of 67.9% does not suggest a strong degree of evidence in favor of an effect. During the post-test, those receiving iPrEP were less ready to take PrEP than those receiving UC.
Findings suggest that iPrEP increased knowledge about the PrEP medication but had a negative impact on readiness to take PrEP relative to UC. It is imperative that future research among cisgender Black women carefully considers the content provided in interventions designed to increase PrEP use, balancing the benefits of PrEP with the side effects and daily pill burden.
clinicaltrial.gov Identifier: NCT03930654, 29/04/2019.
在美国,跨性别(cis)黑人女性一生中感染艾滋病毒的可能性比其他女性更高。我们开发并实施了一种行为干预措施,即增加 PrEP(iPrEP),这是首个旨在激励 cis 黑人女性愿意使用 PrEP 进行艾滋病毒预防并在急诊就诊后首次参加 PrEP 诊所就诊的试点随机对照试验(RCT)。
符合条件的参与者为年龄在 18-55 岁之间的黑人 cis 女性,她们承认最近有无保护性行为和药物使用。参与者被随机分配到 iPrEP 或常规护理(UC)组。iPrEP 是一项基于调查的干预措施,旨在提高对 PrEP 的认识和了解。参与者在干预前后完成了对 PrEP 的知识和意愿的评估,然后获得了热情的转介,转介到当地的 PrEP 诊所。入组的参与者被随访 6 个月。
40 名入组参与者的年龄在 18-54 岁之间。教育水平在一些高中教育和研究生教育之间均匀分布。大多数参与者是单身(n=25)或已婚(n=7)。22 名参与者全职就业。预测试结果表明,40 名参与者中有 21 名听说过 PrEP。所有参与者都将 PrEP 确定为一种每日艾滋病毒预防药物。对于随机分配到 iPrEP 的参与者,在控制基线的情况下,在 post-test 中了解 PrEP 的可能性高于 UC(OR=5.22,95%CrI=0.50,94.1)。iPrEP 对意愿的影响与 UC 相比没有任何差异。iPrEP 对意愿的估计略高(4.16 与 4.04;即高 0.12 分);然而,67.9%的后验概率并没有表明在支持效果方面有很强的证据。在 post-test 中,接受 iPrEP 的人比接受 UC 的人准备接受 PrEP 的意愿较低。
研究结果表明,iPrEP 增加了对 PrEP 药物的了解,但与 UC 相比,对接受 PrEP 的意愿产生了负面影响。cis 黑人女性中开展的未来研究必须仔细考虑旨在增加 PrEP 使用的干预措施中提供的内容,平衡 PrEP 的益处与副作用和每日药丸负担。
clinicaltrial.gov 标识符:NCT03930654,2019 年 4 月 29 日。