NCT05390567Recruiting
Project CONTINUITY: Promoting Evidence-Based Cancer Screening Among Underserved Women
Source: ClinicalTrials.gov · Last updated 6 Aug 2026
Brief summary (registry, in English)
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).
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 800 (estimated)
- First submitted
- 19 May 2022
- Start date
- 7 Jun 2024
- Primary completion date
- 1 May 2027
- Lead sponsor
- University of Florida
- Diseases
- Cervical cancer
- NCT number
- NCT05390567
What you commit to
- Study type: Observational
- Planned participants: 800
- From 7 Jun 2024 to the primary completion date, 1 May 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.
Other
- For patients who are excluded for criterion 6, 7, and 8, the outreach team (community clinical navigator and CHW) will ask the participant if they can be re-contacted for potential future study eligibility assessment. If the participant agrees, the navigator or CHW will collect contact information to re-contact the participant at a later (pre-determined) date up to 20 weeks later for eligibility screening.
Who the study is looking for
- Using the American Cancer Society (ACS) screening recommendations, adults 25 to 65 will be eligible.
- Assigned sex at birth is female
- No previous history of cervical cancer
- No previous history of a hysterectomy
- Not currently pregnant (self-report)
- Not currently menstruating\*
- Have not used any vaginal products (e.g., oil-based lubricants, antifungal, and douches) in prior 2 days\*. Use of vaginal contraceptives, condoms and water-based lubricants are allowed.
- Have not given birth in the prior 12 weeks\*
- Self-report they have not undergone cancer screening in the past 4 years or more OR report being past due according to provider recommended screening schedule.
- Self-report of using the MOC in the past, no current usual source of care OR usual source of care is a non-UFH provider and/or cervical cancer screening is not accessible through that provider
- Reside in census tracts where the Mobile Outreach Clinic travels.
- Have a mobile phone or access to a mobile phone that can be used to receive messages or a valid email address.
Age in the registry: 25 years to 65 years · Sex: Female · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Florida Coordinator of this site? Confirm its status | Gainesville | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.