Actively Recruiting

Phase Not Applicable
Age: 30Years - 65Years
FEMALE
Healthy Volunteers
NCT06825689

Unidos Contra el VPH

Led by University of Texas at Austin · Updated on 2025-02-13

735

Participants Needed

1

Research Sites

209 weeks

Total Duration

On this page

Sponsors

U

University of Texas at Austin

Lead Sponsor

T

Texas Tech University Health Sciences Center, El Paso

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Unidos Contra el VPH

Who Can Participate

Age: 30Years - 65Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals with a cervix who are 30-65 years old
  • Have not had a Pap test in at least three years
Not Eligible

You will not qualify if you...

  • Having had a hysterectomy
  • Personal history of cervical cancer

AI-Screening

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Trial Site Locations

Total: 1 location

1

Project Vida Health Center

El Paso, Texas, United States, 79905

Actively Recruiting

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Research Team

J

Jessica Calderón-Mora, DrPH

CONTACT

Y

Yanneth Rivera, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

3

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