Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.

Part of paid clinical trials in Gainesville, Florida.

Sponsor
University of Florida
Study ID
NCT07351110
Status
Recruiting

Conditions

  • Cervical Cancer (Early Detection)
  • Diabetes
  • Obesity & Overweight

Eligibility Criteria

Sex
FEMALE
Age
25 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • patient navigation and self-collection — BEHAVIORAL
    Patients will receive a combination of patient navigation, education, and cervical cancer self-collection sampling as part of the intervention to support cervical cancer screening.

Study Details

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.

Key Dates

First listed
Jan 20, 2026
Start date
Jun 30, 2026
Status verified
Jan 2026
Primary completion
Dec 30, 2026
Completion
Mar 24, 2027

Study Design

Enrollment
20 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING

Arms

  • Experimental: Intervention
    PINPOINT intervention arm will entail assigning patients to a patient navigator to assist them with screening reminders and address any barriers they have to screening, education on cervical cancer screening, and patients will also be offered the opportunity to self-collect their sample for cervical cancer screening.
  • No Intervention: Control Arm
    No intervention arm, patients will receive reminders for screening according to current clinical practice

Primary Outcome Measure

Cervical cancer screening [ Time Frame: within 6 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
UF Health Internal MedicineGainesvilleFlorida32611
Dianne G Goede, MD
352-265-0140
Dianne L Goede, MD (PRINCIPAL_INVESTIGATOR)

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