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Developing and Implementing HPV SCREENED
Developing and Implementing HPV SCREENED (Self-Collection REach and ENgagement in Emergency Departments) to Improve Cancer Equity
Who can join
Ages 30 to 65 · Women · Healthy volunteers welcome
Full eligibility criteria
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
About the study
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.
What is being tested
- HPV Self-collection in the ED (behavioral)
Sponsor: Rutgers, The State University of New Jersey · Participants: 100 · Started: Oct 15, 2026
Contact the study team
- Sara Heinert, PhD, MPH · Phone: (732) 235-7872
Official record on ClinicalTrials.gov — NCT07657104
Locations in the U.S.
| New Jersey | Robert Wood Johnson University Hospital, New Brunswick University Hospital, Newark (Not yet recruiting) |
From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.