Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age25+
SponsorUniversity of Florida
About this trial
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 criteria
Qualifiers
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
Disqualifiers
Previous history of cervical cancer
Total hysterectomy
Pregnant
Trial design
Treatments tested in this trial
- patient navigation and self-collection
Treatment groups
20 Participants
are divided into 2 treatment groupsSponsors and collaborators
University of Florida
Lead sponsor
National Cancer Institute (NCI)
Collaborator
Source ClinicalTrials.gov