Home › Cervical Cancer › NCT06825689
Unidos Contra el VPH
Unidos Contra el VPH: Screening Preference and Uptake of HPV Self-sampling Among Latinxs Along the US-Mexico Border
Who can join
Ages 30 to 65 · Women · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Individuals with a cervix who are 30-65 years and have not undergone a Pap test in at least three years. Exclusion Criteria: * Having had a hysterectomy or a personal history of cervical cancer.
About the study
The purpose of the Unidos Contra el VPH study is to help find options to screen, or check, for cervical cancer that individuals can do at home to help prevent and detect cervical cancer early. Usually, people get screened for cervical cancer with a Pap smear and human papillomavirus (HPV) test by a health care provider. This is not always easy for individuals who are not able to get to a clinic or feel uncomfortable having the procedure done. That is why we want to find other ways that may be easier and more comfortable for people to be screened for cervical cancer.
The two main questions the study aims to answer are:
1. How do the following three cervical cancer screening methods compare for improving screening completion rates?
o In-home HPV self-sampling with a vaginal swab * In-home HPV self-sampling with urine testing * In-clinic traditional Pap smear with HPV test 2. What are participant beliefs and preferences regarding these three screening methods?
Participants in the study will be randomly assigned to one of three groups. This means each person has an equal chance of being placed in any group. They will also complete two surveys as part of the study. The three screening method groups are described below:
Group 1: Urine Self-Sampling * Participants in this group will receive a kit with a urine sample cup to use at home, instructions explaining how to take the sample and a pre-paid mailing box to mail the urine sample to the lab.
Group 2: Vaginal Swab Self-Sampling o Participants in this group will receive a kit with a vaginal swab and collection tube to use at home, instructions explaining how to take the sample and a pre-paid mailing box to mail the sample to the lab.
Group 3: In-Clinic Screening * An in-clinic co-testing appointment is scheduled for a Pap smear and HPV test done together at Project Vida Health Center.
By comparing these approaches, this study aims to improve access to cervical cancer screening and provide better options for those who face barriers to clinic-based screening.
What is being tested
- Self-sampling with urine (device)
- Self-sampling with swab (device)
- In-clinic Pap/HPV co-testing (device)
Sponsor: University of Texas at Austin · Participants: 735 · Started: Jan 28, 2025
Contact the study team
- Jessica Calderón-Mora, DrPH · Phone: 915-443-0272
- Yanneth Rivera, MPH · Phone: 512-417-9617
Official record on ClinicalTrials.gov — NCT06825689
Locations in the U.S.
| Texas | Project Vida Health Center, El Paso |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.