Feasibility of HPV Self-Collection Kits for Cervical Cancer Screening

Recruiting N/A Interventional Study
Cervical Cancer HPV Infection
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
25 and older
Sex
Female
Study type
Interventional
Purpose
Health Services Research
Participants needed
100 (estimated)
Sponsor
Washington University School of Medicine · Other
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Are age 25 or older * Has an intact cervix * Self-reports that they have not been screened for cervical cancer within the last 3 years for 25-64, 5 years for 65 or older * Has a cellphone that can receive texts (including verification codes) and an email account * Has access t…
Contacts

Michelle Silver, PhD, ScM

314-454-7903

michelle.silver@wustl.edu

CONTACT