Developing and Implementing HPV SCREENED
Starting soon · Not applicable
Conditions studied: Cervical Cancer Screening, Human Papilloma Virus
In brief
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.
Key facts
- Study ID
- NCT07657104
- Run by
- Rutgers, The State University of New Jersey
- People needed
- 100
- Starts
- 2026-07-01
- Expected to finish
- 2027-09-30
- Last updated by the study team
- 2026-06-18
Who can join
Age: 30 and older, up to 65. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- 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
You may not qualify if…
- currently pregnant (as diagnostic procedures for cervical cancer are often deferred during pregnancy);
- previous hysterectomy;
- previous diagnosis of cervical cancer;
- current menses
Where it is running
- Robert Wood Johnson University Hospital — New Brunswick, New Jersey, United States
- University Hospital — Newark, New Jersey, United States
Full record on ClinicalTrials.gov
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