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Recruiting NCT07657104

NCT07657104 Developing and Implementing HPV SCREENED

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Clinical Trial Summary
NCT ID NCT07657104
Status Recruiting
Phase —
Sponsor Rutgers, The State University of New Jersey
Condition Cervical Cancer Screening
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2026-10-15
Primary Completion 2027-06-30

Eligibility & Interventions

Sex Female only
Min Age 30 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
HPV Self-collection in the ED

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2026-10-15 with a primary completion date of 2027-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

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

Contact & Investigator

Central Contact

Sara Heinert, PhD, MPH

✉ sara.heinert@rutgers.edu

📞 (732) 235-7872

Principal Investigator

Sara Heinert, PhD, MPH

PRINCIPAL INVESTIGATOR

Department of Emergency Medicine, Rutgers Robert Wood Johnson Medical School

Frequently Asked Questions

Who can join the NCT07657104 clinical trial?

This trial is open to female participants only, aged 30 Years or older, up to 65 Years, studying Cervical Cancer Screening. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07657104 currently recruiting?

Yes, NCT07657104 is actively recruiting participants. Contact the research team at sara.heinert@rutgers.edu for enrollment information.

Where is the NCT07657104 trial being conducted?

This trial is being conducted at New Brunswick, United States, Newark, United States.

Who is sponsoring the NCT07657104 clinical trial?

NCT07657104 is sponsored by Rutgers, The State University of New Jersey. The principal investigator is Sara Heinert, PhD, MPH at Department of Emergency Medicine, Rutgers Robert Wood Johnson Medical School. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology