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.
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