Actively Recruiting

Phase 4
Age: 9Years +
All Genders
Healthy Volunteers
NCT07015957

Kupewa: Optimizing Implementation Strategies for Cervical Cancer Prevention

Led by New York University · Updated on 2026-04-30

7000

Participants Needed

1

Research Sites

212 weeks

Total Duration

On this page

Sponsors

N

New York University

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Kupewa: Optimizing Implementation Strategies for Cervical Cancer Prevention

Who Can Participate

Age: 9Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Health workers who provide medical care or counseling and interact with adolescent girls and young women aged 9-24 and/or their parents or caregivers
  • Non-pregnant females aged 9-24 receiving HIV care at a participating health facility during the study period
  • For participants aged 9-17, their male or female parent or guardian is also eligible to participate
Not Eligible

You will not qualify if you...

  • Health workers younger than 18 years, not actively providing regular care or counseling at the facility, or unwilling or unable to provide informed consent
  • Clients younger than 9 years or older than 24 years
  • Pregnant individuals
  • Individuals unable or unwilling to provide informed consent

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Partners in Hope

Lilongwe, Malawi

Actively Recruiting

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Research Team

C

Corrina Moucheraud

CONTACT

R

Risa M Hoffman

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

8

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Kupewa: Optimizing Implementation Strategies for Cervical Cancer Prevention | DecenTrialz