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NCT07351110Recruiting

Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.

Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions. Aim 3: Assess the Feasibility and Acceptability of the PINPOINT Intervention.

Source: ClinicalTrials.gov · Last updated 10 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
16 Jan 2026
Start date
30 Aug 2026
Primary completion date
31 Dec 2027
Lead sponsor
University of Florida
NCT number
NCT07351110

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 30 Aug 2026 to the primary completion date, 31 Dec 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.

Prior treatment

  • Previous history of cervical cancer

Other

  • Total hysterectomy
  • Pregnant

Who the study is looking for

  • The following eligibility criteria will be used to determine inclusion into the study:
  • 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
  • Have not undergone cancer screening in the past 3 years or more
  • Reside in the UFHCI Catchment Area (Alachua, Baker, Bradford, Citrus, Clay, Columbia, Dixie, Gadsden, Gilchrist, Hamilton, Jefferson, Lafayette, Lake, Leon, Levy, Madison, Marion, Putnam, Sumter, Suwannee, Taylor, UnioF1n, or Wakulla County).
  • Have a mobile phone or access to a mobile phone that can be used to receive messages, or a valid email address.
  • Are not currently scheduled to receive cervical cancer screening via clinician sampling (pap smear).

Age in the registry: 25 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UF Health Internal Medicine
Coordinator of this site? Confirm its status
GainesvilleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.