Clinical trial
Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.
Recruiting now · Not applicable · 1 countries · Registry ID NCT07351110
Recruiting nowNot applicableInterventional
What this study is about
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.
A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.
Basic eligibility
Age25 Years to Not listed
SexFemale
Healthy volunteersAccepted
ConditionDiabetes, Cervical Cancer (Early Detection), Obesity & Overweight
Full registry criteria
Inclusion Criteria: The following eligibility criteria will be used to determine inclusion into the study: 1. Using the American Cancer Society (ACS) screening recommendations, adults aged over the age of 25 will be eligible 2. Active UF Internal Medicine patient and has had an appointment in the last 2 months. 3. Assigned sex at birth is female 4. Have Obesity or Type 2 Diabetes 5. Not currently pregnant (self-report) 6. Have not given birth in the prior 12 weeks 7. No previous history of cervical cancer 8. No previous history of a hysterectomy 9. Have not undergone cancer screening in the past 3 years or more 10. 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). 11. Have a mobile phone or access to a mobile phone that can be used to receive messages, or a valid email address. 12. Are not currently scheduled to receive cervical cancer screening via clinician sampling (pap smear). Exclusion Criteria: * Previous history of cervical cancer * Total hysterectomy * Pregnant
Treatments and study arms
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.
Primary outcomes
Cervical cancer screeningwithin 6 months
receiving cervical cancer screening either via self-collection, pap smear, or hpv testing
Study locations
1 locations were listed when this page was built. The first 40 are shown.
UF Health Internal Medicine🇺🇸 Gainesville, Florida, United States
Dianne G Goede, MDContact
Dianne L Goede, MDPrincipal Investigator