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Developing and Implementing HPV SCREENED

Rutgers, The State University of New Jersey · NCT07657104

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 30–65 · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
100
US sites recruiting
1
Study start
October 15, 2026
Record last updated
October 22, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: HPV Self-collection in the ED

Conditions: Cervical Cancer Screening; Human Papilloma Virus

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full 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

Recruiting US locations

  • Robert Wood Johnson University Hospital

    New Brunswick, NJ 08901

    Site contact: Sara Heinert, PhD, MPH

Study contacts (from the official record)

  • Sara Heinert, PhD, MPH · (732) 235-7872 · sara.heinert@rutgers.edu
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Developing and Implementing HPV SCREENED (NCT07657104) | Bored Studies