Not Yet RecruitingNot Applicable

Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.

United States20 participantsStarted 2026-03-15

Plain-language summary

Our overarching goal is to adapt and test the PINPOINT intervention -PatIent Navigation for the Prevention of CervIcal CaNcer inTervention. We will test the PINPOINT intervention among patients with high-risk profiles for cervical cancer who do not meet the recommended screening for cervical cancer.

Who can participate

Age range25 Years

SexFEMALE

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Inclusion criteria

✓. Using the American Cancer Society (ACS) screening recommendations, adults aged over the age of 25 will be eligible
✓. Active UF Internal Medicine patient and has had an appointment in the last 2 months.
✓. Assigned sex at birth is female
✓. Have Obesity or Type 2 Diabetes
✓. Not currently pregnant (self-report)
✓. Have not given birth in the prior 12 weeks
✓. No previous history of cervical cancer
✓. No previous history of a hysterectomy

What they're measuring

Cervical cancer screening

Timeframe: within 6 months

Trial details

NCT IDNCT07351110

SponsorUniversity of Florida

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-09-15

Contact for this trial

Rahma Mkuu, PhD

(352) 294-8419 rmkuu@ufl.edu

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