Developing and Implementing HPV SCREENED

Part of paid clinical trials in New Brunswick, New Jersey.

Sponsor
Rutgers, The State University of New Jersey
Study ID
NCT07657104
Status
Not Yet Recruiting

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Conditions

  • Cervical Cancer Screening
  • Human Papilloma Virus

Eligibility Criteria

Sex
FEMALE
Age
30 Years - 65 Years
Healthy Volunteers
Accepted

Interventions

  • HPV Self-collection in the ED — BEHAVIORAL
    Participants will be asked to collect a vaginal sample for HPV screening.

Study Details

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 Dates

Start date
Jul 1, 2026
Status verified
Jun 2026
Primary completion
Jun 30, 2027
Completion
Sep 30, 2027

Study Design

Enrollment
100 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING

Arms

  • Other: HPV SCREENED
    A single-arm pilot trial of HPV self-sampling among under-screened women in the ED

Primary Outcome Measure

Completion of ED-Based HPV Self-Sampling [ Time Frame: Day 1 ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Robert Wood Johnson University HospitalNew BrunswickNew Jersey08901
Sara Heinert, PhD, MPH
University HospitalNewarkNew Jersey07103
Ronald Ikechi, MD

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