RecruitingNot ApplicableNCT07351110

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.

Sponsor

University of Florida

Enrollment

20 participants

Start Date

Jun 30, 2026

Study Type

INTERVENTIONAL

Conditions

Obesity, Overweight Diabetes Cervical Cancer (Early Detection)

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.

Eligibility

Sex: FEMALEMin Age: 25 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a behavioral approach called patient navigation and self-collection for people with cervical cancer (early detection), diabetes, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 25 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALpatient navigation and self-collection

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.

Locations(1)

UF Health Internal Medicine

Gainesville, Florida, United States

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