Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions.
Improving Cervical Cancer Prevention Among Women Living With Chronic Conditions. Aim 3: Assess the Feasibility and Acceptability of the PINPOINT Intervention.
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 25 Years and older
- Sex
- Female only
- Healthy volunteers
- Accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study tests PINPOINT, a program to help patients get screening tests to prevent cervical cancer. It is for women with obesity or type 2 diabetes who have a high risk of cervical cancer and are overdue for screening.
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.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Be older than 25 and assigned female at birth.
- Be a current UF Internal Medicine patient with a visit in the past 2 months.
- Have obesity (too much body fat) or type 2 diabetes (a condition that causes high blood sugar).
- Not be pregnant and not have given birth in the past 12 weeks.
- Have no history of cervical cancer or a hysterectomy (surgery to remove the uterus).
- Have had no cancer screening for at least 3 years and have no Pap test scheduled with a clinician.
- Live in one of these Florida counties: Alachua, Baker, Bradford, Citrus, Clay, Columbia, Dixie, Gadsden, Gilchrist, Hamilton, Jefferson, Lafayette, Lake, Leon, Levy, Madison, Marion, Putnam, Sumter, Suwannee, Taylor, Union, or Wakulla.
- Have access to a mobile phone that can receive messages, or have a valid email address.
Who can't join
- Have had cervical cancer.
- Have had a total hysterectomy (surgery to remove the uterus and cervix).
- Are pregnant.
Simplified for readability. The official criteria below are what the study team uses.
Official 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 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
Study sites (1)
FL
- UF Health Internal Medicine · Gainesville, FL 32611Dianne G Goede, MD · Study contact · 352-265-0140 · diannelroberts@ufl.eduDianne L Goede, MD · Principal investigatorMore trials in Gainesville