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NCT07015957Active, not recruitingPhase 4

Kupewa: Optimizing Implementation Strategies for Cervical Cancer Prevention

Source: ClinicalTrials.gov · Last updated 5 Aug 2026

Brief summary (registry, in English)

The goal of this clinical trial is identify an effective and implementable set of implementation strategies to increase cervical cancer prevention in Malawi. The main questions it aims to answer are: 1. Which implementation strategies produce the greatest increase in provider recommendation for, and uptake of, cervical cancer prevention tools among people receiving HIV care. 2. What is the acceptability, appropriateness, feasibility, and cost of these implementation strategies. 3. What is the sustained effect of these implementation strategies. The implementation strategies will be conducted with health workers (clinical officers, nurses, and medical assistants): training, coaching, and a reminder system.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
7000 (estimated)
First submitted
3 Jun 2025
Start date
8 Jul 2025
Primary completion date
Aug 2027
Lead sponsor
New York University
NCT number
NCT07015957

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 7000
  • From 8 Jul 2025 to the primary completion date, Aug 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • Health workers: Less than 18 years of age, or not an active and regular provider of medical care or counseling at the facility, or unable or unwilling to provide informed consent.
  • Clients: \<9 or \>24 years old, or pregnancy, or unable or unwilling to provide informed consent.

Who the study is looking for

  • Health workers: People who provide medical care and counseling (typically medical assistants, clinical officers, and nurses), and interact with adolescent girls and young women aged 9-24 and/or their parents/caregivers.
  • Clients: Non-pregnant females aged 9-24 (for those aged 9-17, their male or female parent/guardian will also be eligible for participation) who present for HIV care at a participating health facility during the study period.

Age in the registry: 9 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Partners in Hope
Coordinator of this site? Confirm its status
LilongweMalawiUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.