Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT05882916

Reaching the Last 20% (the Pamoja Kwa Afya Study)

Led by Sue Napierala · Updated on 2025-03-18

5000

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

Sponsors

S

Sue Napierala

Lead Sponsor

I

Impact Research & Development Organization

Collaborating Sponsor

AI-Summary

What this Trial Is About

This cluster randomized controlled trial will test whether the provision of multiple oral fluid-based HIV self-test kits to women who sell sex (WSS) to secondarily distribute to their male partners who purchase sex can promote uptake of HIV service use by male partners. The study will recruit adult women who report exchanging sex for compensation in Kisumu and Siaya counties in Western Kenya. In clusters randomized to the intervention, WSS will be given multiple HIV self-tests and counseled to distribute them to men who purchase sex (MPS). Self-test kits will contain instructions for use and tailored information on clinic location and hours within the cluster, and pilot-tested messaging on the benefits of antiretroviral therapy (ART) and pre-exposure prophylaxis (PrEP). In control clusters, standard of care HIV services will continue to be available. To objectively assess impacts of the intervention on post-HIVST linkage outcomes, the investigators will monitor use of HIV services by men at HIV clinics in both study arms on a monthly basis. Our goal will be to determine whether confirmatory testing (primary outcome), case diagnoses, ART initiation, and PrEP initiation by men in intervention clusters are higher than in control clusters. Mixed methods research will be utilized to conduct a process evaluation to assess mechanisms that may have impacted intervention effectiveness, pathways for linkage among MPS, and support for men's linkage to HIV services under a secondary distribution model. Cost-effectiveness analyses will also be undertaken.

CONDITIONS

Official Title

Reaching the Last 20% (the Pamoja Kwa Afya Study)

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female
  • Age 18 years or older
  • Reports exchanging sex for compensation with 2 or more men in the past month
  • Engages in sex for compensation in the intervention cluster catchment area
  • Willing to participate in a brief questionnaire 6 weeks after enrollment
  • Plans to remain in the area of study recruitment for the next 8 weeks
Not Eligible

You will not qualify if you...

  • Unwilling or unable to provide informed consent for participation

AI-Screening

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Trial Site Locations

Total: 1 location

1

Impact Research and Development Organization (IRDO)

Kisumu, Kenya

Actively Recruiting

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Research Team

S

Sue Napierala, PhD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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