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← Trials
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Developing and Implementing HPV SCREENED

RecruitingNAAges 30 Years - 65 YearsFemaleRutgers, The State University of New Jersey
NCT07657104 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This study will assess the feasibility of implementing HPV self-sampling as a primary cervical cancer screening strategy for under-screened women in the emergency department (ED). Eligible participants will receive education and an HPV self-sampling kit to complete in the ED. Individuals with HPV-positive results will be guided to follow-up care at a local clinic.

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📋 Eligibility rules (as published)
Inclusion Criteria: * biological women, * no prior hysterectomy or cervical cancer, * not pregnant, * last Pap \>3 years, last co-test \>5 years, or last HPV alone test \>5 years, * speak English or Spanish, * has a working cellphone, * NJ residency * ED patient Exclusion Criteria: * currently pregnant (as diagnostic procedures for cervical cancer are often deferred during pregnancy); * previous hysterectomy; * previous diagnosis of cervical cancer; * current menses
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What it tests

  • HPV Self-collection in the ED
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Where

2 sites
Robert Wood Johnson University Hospital
New Brunswick, United States
University Hospital
Newark, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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