Actively Recruiting
Project CONTINUITY: Promoting Evidence-Based Cancer Screening Among Underserved Women
Led by University of Florida · Updated on 2025-07-11
800
Participants Needed
1
Research Sites
181 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Project CONTINUITY (Connecting You to Care in the Community) was developed to increase adherence to cervical cancer screening regimens from initial screening to needed follow-up care by (1) providing personalized approaches to improve adherence through the combined use of patient choice for the initial screening method (Pap/HPV co-testing vs. HPV self-test collection), community clinical navigators and community health workers (CHWs), customized messages and support for patient portal access for test results and (2) implementing strategies to address social determinants of health (SDoH) that may influence an individual's ability to adhere to the screening regimen, with an initial focus on removing transportation barriers through the use of a mobile outreach clinics (MOC).
CONDITIONS
Official Title
Project CONTINUITY: Promoting Evidence-Based Cancer Screening Among Underserved Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 25 to 65 years following American Cancer Society screening recommendations
- Assigned female sex at birth
- No previous history of cervical cancer
- No previous history of a hysterectomy
- Not currently pregnant (self-report)
- Not currently menstruating
- No use of vaginal products such as oil-based lubricants, antifungal, or douches in prior 2 days (water-based lubricants, condoms, and vaginal contraceptives are allowed)
- No childbirth in the prior 12 weeks
- Not screened for cervical cancer in the past 4 years or more OR past due for screening per provider recommendations
- Previous use of the Mobile Outreach Clinic, no current usual source of care, or usual care provider does not offer cervical cancer screening
- Reside in census tracts served by the Mobile Outreach Clinic
- Have access to a mobile phone or valid email to receive messages
You will not qualify if you...
- Currently menstruating
- Use of vaginal products such as oil-based lubricants, antifungal, or douches in prior 2 days
- Childbirth within the prior 12 weeks
For women excluded due to menstruation, recent vaginal product use, or recent childbirth, the outreach team may ask permission to re-contact for future eligibility up to 20 weeks later.
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Trial Site Locations
Total: 1 location
1
University of Florida
Gainesville, Florida, United States, 32610
Actively Recruiting
Research Team
J
Jamie Barrow, MHA, CCRP
CONTACT
J
Jennifer N Woodard, MPH, CCRP
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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