This study is testing an intervention called PINPOINT (PatIent Navigation for the Prevention of CervIcal CaNcer inTervention) to help women at high risk for cervical cancer get screened. The PINPOINT intervention combines patient navigation (guidance and support), education, and self-collection of samples for cervical cancer screening. The goal is to see if this approach increases cervical cancer screening rates within six months. You may be able to join if you are a woman over 25, an active UF Internal Medicine patient, and have obesity or Type 2 diabetes. The study aims to enroll 20 participants, but its current status is unclear.

Study design

This is an interventional study that plans to enroll 20 participants. It is not specified if it is randomized or blinded.

What's involved

Patients will receive patient navigation, education, and cervical cancer self-collection sampling as part of the intervention.

Compensation

Not stated in the trial record.

Follow-up

Cervical cancer screening will be measured within 6 months after the intervention.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.