Actively Recruiting

Phase Not Applicable
Age: 25Years - 65Years
FEMALE
Healthy Volunteers
NCT07453459

Feasibility of HPV Self-Collection Kits for Cervical Cancer Screening

Led by Washington University School of Medicine · Updated on 2026-04-23

100

Participants Needed

1

Research Sites

91 weeks

Total Duration

On this page

Sponsors

W

Washington University School of Medicine

Lead Sponsor

T

Teal Health, Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study is testing and implementing an equity-focused, community-based intervention that improves women's access to cervical cancer screening and adherence to follow up after an abnormal result. The study's objective is to assess and compare the feasibility of different methods of distributing at-home HPV testing kits for cervical cancer screening among individuals who are under-screened.

CONDITIONS

Official Title

Feasibility of HPV Self-Collection Kits for Cervical Cancer Screening

Who Can Participate

Age: 25Years - 65Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Are age 25-65
  • Have an intact cervix
  • Have not had cervical cancer screening within the last 3 years
  • Have a smartphone
  • Have internet access to use the Teal Health mobile app and complete a Zoom interview
  • Can read, speak, write, and understand English well enough to take a survey and complete an interview
Not Eligible

You will not qualify if you...

  • Have abnormal vaginal bleeding or discharge
  • Have a history of cancer of the reproductive system
  • Have a compromised immune system
  • Have prior Diethylstilbestrol (DES) exposure
  • Are currently pregnant or within 6 weeks of giving birth
  • Have had treatment for cervical precancer (e.g., loop electrosurgical excision procedure or conization) in the last 25 years

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Trial Site Locations

Total: 1 location

1

Washington University School of Medicine

St Louis, Missouri, United States, 63110

Actively Recruiting

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Research Team

M

Michelle Silver, PhD, ScM

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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