Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.
Recruiting
N/A
Interventional Study
Diabetes
Cervical Cancer (Early Detection)
Obesity & Overweight
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 25 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 20 (estimated)
- Sponsor
- University of Florida · Other
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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.
Trial Locations
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Eligibility 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 …
Contacts