Actively Recruiting
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
Eligibility Criteria
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
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
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Washington University School of Medicine
St Louis, Missouri, United States, 63110
Actively Recruiting
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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