Home screening options for cervical cancer
Unidos Contra el VPH: Screening Preference and Uptake of HPV Self-sampling Among Latinxs Along the US-Mexico Border
This study is testing if home screening methods for cervical cancer, like using vaginal swabs and urine tests, are as effective as traditional clinic visits to help more people get screened.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 735 (estimated) |
| Ages | 30 Years to 65 Years |
| Sex | Female |
| Sponsor | University of Texas at Austin Academic / other |
| Locations | 1 site (El Paso, Texas) |
| Trial ID | NCT06825689 on ClinicalTrials.gov |
What this trial studies
The Unidos Contra el VPH initiative aims to explore alternative methods for cervical cancer screening that individuals can perform at home. The study compares the effectiveness of in-home HPV self-sampling using vaginal swabs and urine tests against traditional in-clinic Pap smears with HPV testing. By assessing these methods, the study seeks to improve screening completion rates and understand participant beliefs and preferences regarding these options. This approach addresses barriers faced by individuals who may find it difficult or uncomfortable to visit a clinic for screening.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 30-65 with a cervix who have not had a Pap test in the last three years.
Not a fit: Patients who have had a hysterectomy or a personal history of cervical cancer will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide more accessible and comfortable screening options for cervical cancer, potentially increasing early detection rates.
How similar studies have performed: Other studies have shown promise in using self-sampling methods for HPV screening, indicating that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion 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.
Where this trial is running
El Paso, Texas
- Project Vida Health Center — El Paso, Texas, United States (Recruiting)
Study contacts
- Study coordinator: Jessica Calderón-Mora, DrPH
- Email: jessica.calderonmora@austin.utexas.edu
- Phone: 915-443-0272
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.