在大型艾滋病毒预防临床试验FEM-PrEP中实施经验知情的招募方法的经验教训

IF 1.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Caleb Parker, A. Corneli, K. Agot, Jacob Odhiambo, Jesse Asewe, Khatija Ahmed, Joseph Skhosana, Malebo Ratlhagana, Michele Lanham, Christina Wong, J. Deese, Rachel Manongi, L. Damme
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引用次数: 1

摘要

我们实施了一项基于经验的、基于地理位置的FEM-PrEP招募方法,这是一项人类免疫缺陷病毒(HIV)预防临床试验,每日口服恩替他滨(FTC)和富马酸替诺福韦二吡酯(TDF)预防HIV。在形成性研究阶段,我们对地方艾滋病控制工作重点(PLACE)方法进行了修改,并利用这些数据和工作人员的经验来确定和优先考虑艾滋病毒感染率可能高的地理区域。在临床试验期间,我们在形成性研究中确定的地理区域实施了常规监测和灵活的招募计划。我们描述了从实施这一方法中获得的三个经验教训:1)地点数据对于确定被认为是高风险的地方至关重要;2)需要将员工经验与PLACE数据结合起来,为实际的招聘策略提供信息;3)在PLACE数据确定的重点地区的机构招募人员,导致Bondo站点(肯尼亚)对许多艾滋病毒阳性妇女进行筛查,给诊所工作人员带来额外负担。这些经验教训突出了具有灵活和受监测的征聘战略的极端重要性。虽然我们成功地招募了HIV高风险人群,但由于参与者对研究产品的依从性较低,FEM-PrEP无法确定FTC/TDF预防HIV的有效性。我们必须将新产品临床试验的招募模式从关注确定高发病率人群转变为确定有动力并能够坚持研究产品方案的风险人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lessons learnt from implementing an empirically informed recruitment approach for FEM-PrEP, a large HIV prevention clinical trial
: We implemented an empirically informed, geographically based recruitment approach for FEM-PrEP, a human immunodeficiency virus (HIV) prevention clinical trial of daily oral emtricitabine (FTC) and tenofovir disoproxil fumarate (TDF) for HIV prevention. During the formative research phase, we conducted a modification of the Priorities for Local AIDS Control Efforts (PLACE) method and used those data and staff experiences to identify and prioritize for recruitment geographic areas where HIV incidence might be high. During the clinical trial, we implemented a routinely monitored and flexible recruitment plan in the geographical areas identified in the formative research. We describe three lessons learnt from implementing this approach: 1) the PLACE data were critical in identifying places presumed to be high risk; 2) staff experiences, in combination with PLACE data, were needed to inform a practical recruitment strategy; and 3) recruiting in establishments in priority areas identified by the PLACE data led to screening many HIV-positive women at the Bondo site (Kenya), placing additional burden on clinic staff. These lessons learnt highlight the critical importance of having a flexible and monitored recruitment strategy. Although we successfully recruited a study population at higher risk for HIV, FEM-PrEP was unable to determine the effectiveness of FTC/TDF for HIV prevention, due to low adherence to the study product among participants. We must shift the paradigm of recruitment for clinical trials of new products from focusing on identifying populations with high incidence to identifying populations at risk who are motivated and able to adhere to the study product regimen.
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来源期刊
Open Access Journal of Clinical Trials
Open Access Journal of Clinical Trials MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.90
自引率
0.00%
发文量
2
审稿时长
16 weeks
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