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临床试验/NCT04558554
NCT04558554已完成不适用

Pharmacy Delivery to Expand the Reach of PrEP in Kenya: Pilot Study

University of Washington2 个研究点 分布在 1 个国家目标入组 1,216 人开始时间: 2020年11月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
1,216
试验地点
2
主要终点
PrEP Initiation

研究概览

简要总结

3 consecutive studies to test a novel model for PrEP initiation and refills in Kenya: pharmacy-based PrEP delivery.

详细描述

Pre-Exposure Prophylaxis (PrEP) is a new HIV prevention method that works when taken as recommended. To take full advantage of public health benefit of PrEP for HIV prevention, there is need to prioritize access, minimize costs of delivery, and reach out to at-risk populations. In Africa, PrEP is being added to a public health infrastructure which is sometimes burdened by overcrowding and drug stock outs; the ability of health systems to maximize PrEP access necessitates finding novel delivery strategies. Additionally, there exist major barriers to PrEP delivery, which includes stigma, long waiting times, costs of staffing and healthcare providers' unfamiliarity with delivering prevention interventions. In Kenya, and many other resource-limited countries, retail pharmacies (i.e., chemists) fill an important gap in the health care system providing first stop access to treatment, monitoring and preventive care of urgent and prolonged conditions. Potential PrEP users may desire pharmacy-delivered PrEP over facility-delivered PrEP for reasons including increased convenience, increased privacy and greater engagement compared to health facilities that focus on treating ill patients. Retail pharmacies can offer free, subsidized or affordable healthcare services. The core components of PrEP - including HIV testing, adherence and risk reduction counselling, assessment of side effects and provision of refills - are within the scope of practice for pharmaceutical technologists and pharmacists in Kenya. Prior formative qualitative research and a stakeholder meeting led to development of a care pathway for pharmacy-based PrEP delivery (including initiation and refills), endorsed for piloting in a consultation meeting that included a wide spectrum of regulatory, professional, government, and community stakeholders in Kenya. We will conduct 3 separate, consecutive studies.

During Study 1a (13 months), we will pilot this care pathway in 2 retail pharmacies evenly split between 2 different geographies in Kenya: Kisumu and Thika. Activities will include data collection aimed at potential weak points of pharmacy-based PrEP delivery, in domains relating to acceptability, fidelity, and costs.

During Study 1b (12 months, happening concurrently with Study 1a), we will additionally offer pharmacy-based PrEP refills only to clients who initiated PrEP at select public health clinics, to assess how many clients opt to refill PrEP at a study pharmacy (for a fee) as opposed to at the clinic (for free).

During Study 2 (6 months, happening right after Study 1a), we will modify the delivery model (e.g., add new implementation strategies) to address the weak points identified during Study 1a, and we will expand PrEP delivery to six additional retail pharmacies (for a total of 12 pharmacies), evenly split between Kisumu and Thika.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • •>=18 years
  • •Interested in initiating PrEP at a pilot pharmacy (Study 1a and Study 2), interested in refilling PrEP at a pilot pharmacy (Study 1b), or interested in initiating PEP and/or STI testing at a pilot pharmacy (select pharmacies in Study 2 only)
  • •Initiated PrEP at a project-affiliated clinic (Study 1b only)
  • •Meets all criteria (e.g., tests HIV-negative) on checklist for initiating and/or refilling PrEP (all phases), PEP (Study 2 only), and/or STI testing (Study 2 only)
  • •Able & willing to provide written informed consent

排除标准

  • •Currently pregnant or breastfeeding (Study 1a & 1b only)

研究组 & 干预措施

Study 1a: Pharmacy-based PrEP delivery Pilot (13 months)

Experimental

Participants in this study will have the option to initiate and/or refill pre-exposure prophylaxis (PrEP) at 4 retail pharmacies in Kenya.

干预措施: pharmacy-based PrEP delivery (Other)

Study 1b: Pharmacy-based PrEP delivery Refill (12 months)

Experimental

Participants in this study (happening concurrently with Study 1a) will have the option to refill PrEP at 4 retail pharmacies in Kenya after having initiated PrEP at one of 2 public clinics.

干预措施: pharmacy-based PrEP delivery (Other)

Study 1a: Pharmacy-based PrEP delivery Pilot Extension (6 months)

Experimental

Participants in this study will have the option to initiate and/or refill pre-exposure prophylaxis (PrEP) or initiate PEP at 12 retail pharmacies in Kenya. Additionally, at a subset of 4 pharmacies, participants will have the option to undergo STI testing.

干预措施: pharmacy-based PrEP delivery (Other)

结局指标

主要结局

PrEP Initiation

时间窗: Over 13-month duration of Study 1a and 6-month duration of Study 2

Cumulative number of participants who initiated PrEP at pilot pharmacies (during Study 1a and Study 2) among those eligible for pharmacy PrEP services.

PrEP Retention

时间窗: Over 13-month duration of Study 1a, 12-month duration of Study 1b, and 6-month duration of Study 2

For Study 1a and 2: Percentage of participants who refilled PrEP at a pilot pharmacy, among those who initiated PrEP at a pilot pharmacy. Study 1b: Percentage of participants who refilled PrEP either at a pilot pharmacy or at a pilot clinic, among those who initiated PrEP at a pilot clinic.

次要结局

  • Selection of Pharmacy-based PrEP Refills(During the 12-month duration of Study 1b)
  • STI Testing Uptake(Over 6-month duration of Study 2)
  • Transition From PEP to PrEP(Over 6-month duration of Study 2)
  • PEP Initiation(Over 6-month duration of Study 2)
  • PrEP Initiation Among STI Testing Clients(Over 6-month duration of Study 2)
  • PrEP Adherence(Over 12-month duration of Study 1a and the 6-month duration of Study 2)
  • Selection of Option to Self-administer HIV Risk Assessment Screening Tool(Over 6-month duration of Study 2)

研究者

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

Katrina Ortblad

Affiliate Assistant Professor, Department of Global Health

University of Washington

研究点 (2)

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