Kupewa: Optimizing Implementation Strategies for Cervical Cancer Prevention

Recruiting Phase 4 Interventional Study
Cervical Cancer Prevention
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
9 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Health Services Research
Participants needed
7,000 (estimated)
Sponsor
New York University · Other
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About This Trial
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 accept…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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…
Contacts

Corrina Moucheraud

212-992-6129

c.moucheraud@nyu.edu

CONTACT

Risa M Hoffman

RHoffman@mednet.ucla.edu

CONTACT