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RECRUITING
NCT06674681
NA

HPV Self-Collection Program

Sponsor: University of Utah

View on ClinicalTrials.gov

Summary

The objective of the study is to develop, pilot, and analyze the effectiveness of HPV self-collection programs which will be used to follow up among women overdue for cervical cancer screening. The investigators will develop protocols for in-clinic and home-based HPV-self-collection programs and follow-up system for HPV-positive tests for community health centers and/or clinics. The program is meant to mail HPV-self-collection kits to women who are due and/or overdue for cervical cancer screening and the program is also meant to present women seen in clinic with a self-collection option for screening alongside a Pap test option. The research team will develop related informational resources on how to complete the test as well as information on screening options. The study will neither experiment nor test the effectiveness of the self-collection process nor the assay of specimens for HPV and high-risk HPV strains. It is not a clinical investigation to assess the safety or effectiveness of a medical device. The study is implementation science and seeks to find optimal ways to implement this World Health Organization recommended screening option.

Key Details

Gender

FEMALE

Age Range

25 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

1000

Start Date

2024-10-18

Completion Date

2026-12

Last Updated

2026-02-20

Healthy Volunteers

Yes

Conditions

Interventions

DIAGNOSTIC_TEST

HPV Self-Collection

HPV self-collection program for in-clinic and mailed cervical cancer screening.

Locations (1)

University of Utah Health Hospitals/Huntsman Cancer Institute Population Sciences

Salt Lake City, Utah, United States