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临床试验/NCT03435887
NCT03435887已完成不适用

Piloting At-birth Point of Care HIV Testing Strategies in Kenya

University of Kansas Medical Center6 个研究点 分布在 2 个国家目标入组 1,999 人开始时间: 2016年12月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,999
试验地点
6
主要终点
Proportion of infants tested at 6-weeks

研究概览

简要总结

Innovative strategies to expedite HIV diagnosis among exposed infants, including at-birth testing and two portable point-of-care (POC) diagnostic systems, will be piloted using an implementation framework. The programmatic impact of these tools on early infant diagnosis (EID) will be measured in comparison with parallel standard of care (SOC) HIV DNA PCR testing initiated at 6 weeks of age.

详细描述

Testing HIV-exposed infants by polymerase chain reaction (PCR) testing at 6 weeks is often not early enough to mitigate the substantial mortality peak that occurs around 2-3 months of age. Initial testing at birth would foster more rapid identification of infants with intrauterine (IU) infection and speed up the initiation of antiretroviral therapy (ART) for HIV-positive infants. Consequently, Kenya introduced new early infant diagnosis guidelines recommending at-birth (0-2 weeks) virologic testing in addition to the SOC tests at 6 weeks (6 - <24 weeks), 6 months and 12 months. POC testing performed in the clinic setting can potentially further reduce the time to diagnosis. Investigators will pilot test the implementation, performance, and cost-effectiveness of two POC test systems (Xpert HIV-1 Qual, Alere q HIV-1/2 Detect) in samples from neonates (at-birth test) and older infants (6-week test) in four government hospitals in Kenya.

In the formative phase of the study, interviews will be conducted with parents, providers and community members regarding benefits and concerns about the implementation of at-birth and POC testing. Interviews with parents (pregnant women living with HIV and their partners if available) will focus on the impact for the child and family. Interviews with providers who would carry out POC testing at each site (maternity nurses, mentor mothers, hospital laboratory staff) will highlight issues of training, logistics and implementation. Interviews with community members (parents of HIV-exposed infants, community health workers, community leaders) in surrounding communities will elicit attitudes and suggestions regarding the potential for POC HIV testing in hard to access communities. Investigators will develop a codebook with typical exemplars for each theme, calculating the frequency and distribution of themes within the larger topic areas. The study team will rapidly review themes to inform the POC pilot.

In the intervention phase the investigators will pilot at-birth and POC infant testing strategies in four hospitals over a continuous 12-month enrollment period. Sites will be randomized to pilot Xpert HIV-1 Qual (n=2) or Alere q HIV-1/2 Detect (n=2), both targeting the at-birth and 6-week testing points. A second blood sample will be collected at each time point to be tested by SOC laboratory-based HIV DNA PCR, which will correspond with the Kenya government's 2016 guidelines that recommend adding an at-birth test to the EID schedule. At-birth samples will ideally be collected within 24 hours of delivery and results communicated to the mother with counseling prior to discharge from maternity. The expected due dates of exposed infant will be tracked to encourage mothers who deliver outside the hospital to return for infant testing within two weeks postnatal. Infants enrolled in this pilot will be tracked until HIV results at birth and 6 weeks postnatal have been provided by POC and standard PCR, or until ART is initiated for HIV-positive infants. Investigators will assess user uptake, age at notification of HIV test results, age of ART initiation among HIV+ infants, POC machine performance, costs, and user experiences (providers will participate in a monthly focus group to discuss challenges and solutions) to inform the feasibility and optimal implementation of Kenya's 2016 at-birth test recommendation and of the mobile POC test systems for the improvement of EID outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • HIV-positive pregnant women enrolled in PMTCT services or who deliver at the study hospitals and/or mothers with exposed infants presenting for EID prior to 24 weeks
  • Provide informed consent

排除标准

  • HIV-positive pregnant women less than 18 years of age
  • HIV-positive pregnant women unable to provide informed consent
  • HIV-exposed infants presenting for HIV testing at > 24 weeks

结局指标

主要结局

Proportion of infants tested at 6-weeks

时间窗: 4-12 weeks postpartum

The proportion of infants receiving HIV testing (POC and/or PCR) during the 6 week window

Proportion of infants tested at birth

时间窗: 0-4 weeks

The proportion of infants receiving HIV testing (POC and/or PCR) during the birth testing window

次要结局

  • Infant age at notification of HIV test results (birth and 6 week)(0-8 weeks postnatal)
  • Costs(Month 12)
  • Completeness of POC and SOC tests(up to 24 weeks postnatal)
  • Efficiency of POC and SOC tests(up to 24 weeks postnatal)
  • Retention in EID services(up to 24 weeks postnatal)
  • POC system implementation(Month 12)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sarah Kessler, PhD, MPH

Associate Professor

University of Kansas Medical Center

研究点 (6)

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