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Project CONTINUITY: Promoting Evidence-Based Cancer Screening Among Underserved Women

NCT05390567 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 800

Last updated 2025-07-11

No results posted yet for this study

Summary

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

  • Cervical Cancer Screening Methods

Interventions

BEHAVIORAL

Participant Choice of HPV Self-Test

Opportunity for participants to complete the HPV self-test in a non-clinical setting to be returned via a mailer or courier servie.

BEHAVIORAL

Survey: Participant cancer history and cervical cancer prevention/screening knowledge

Asking women to respond to questions about their cancer history and knowledge of cervical cancer prevention and screening.

BEHAVIORAL

Participant Choice of Standard of Care in-clinic Pap-test

Participant choice of cervical cancer screening method with either a SOC in-clinic pap test or HPV self-test

Sponsors & Collaborators

  • University of Florida

    lead OTHER

Principal Investigators

  • Ramzi A Salloum, PhD · Division Director, Department of Health Outcomes and Biomedical Informatics, University of Florida; Associate Director, Office of Community Outreach and Engagement, UFHealth Cancer Center

Eligibility

Min Age
25 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-06-07
Primary Completion
2027-05-01
Completion
2027-12-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05390567 on ClinicalTrials.gov