Clinical trial Recruiting at 1 site Interventional

Improving HIV prevention and treatment services in family planning clinics

Official title: Systems Analysis and Improvement Approach to Improve Integration of HIV Prevention and Treatment Services

Run by University of Washington · NCT05404958 · Data updated 2026-11-12

This study is testing a new way to improve HIV prevention and treatment services in family planning clinics to see if it helps more young women and new clients get the care they need in Mombasa, Kenya.

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Quick facts

Study typeInterventional
SexAll
Enrollment40 (estimated)
SponsorUniversity of Washington
Academic / other
Locations1 site (Mombasa)
StatusRecruiting
StartedMarch 14, 2024
Main results expectedOctober 1, 2026
Study endsOctober 1, 2027
Registry record updatedMay 4, 2026
Trial IDNCT05404958 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study include new family planning clients and adolescent girls and young women seeking reproductive health services in Mombasa County.

Probably not a fit

Patients who are not seeking family planning services or are from clinics expected to close within the next year may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of the Systems Analysis and Improvement Approach (SAIA) in enhancing the integration of HIV prevention and treatment services within family planning clinics in Mombasa County, Kenya. It involves a cluster-randomized trial comparing SAIA to usual procedures, focusing on increasing HIV counseling, testing, and linkage to care among new family planning clients and adolescent girls and young women. The study will analyze both quantitative and qualitative data using the RE-AIM framework to assess reach, effectiveness, adoption, implementation, and maintenance of the intervention. Additionally, it will estimate the cost and budget impacts of SAIA from a public health perspective.

Why it matters

Potential benefit: If successful, this approach could significantly improve access to HIV prevention and treatment services for women and adolescent girls in East and Southern Africa.

How similar studies have gone: Previous studies using similar integration approaches have shown promise, indicating potential for success in this novel application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

FP clinics:

-All FP clinics that receive County-supplied FP products will be eligible to participate.

FP clinic managers and staff:

-Any FP clinic manager that is 18 years and older is eligible to be interviewed. -These clinic managers can be male or female.

Kenyan public health staff:

* Any Kenyan public health staff that is 18 years and older is eligible to be interviewed.
* These public health staff can be male or female.

Exclusion Criteria:

FP clinics:

* Any clinics that are expected to close within the next year at the time of study initiation
* 12 facilities that participated as SAIA intervention facilities in our small-scale trial where the intervention was led by research staff.

FP clinic managers and staff: No exclusion criteria Kenyan public health staff: No exclusion criteria

Where it's running

  • FP Clinics in Mombasa County
    Mombasa, Kenya
    Recruiting

Study contacts

  • Principal investigator: McKenna Eastment, MD, MPH — University of Washington
  • Study coordinator: McKenna Eastment
  • Email: mceast@uw.edu
  • Phone: 206-4165074

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.