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