HPV Self-Collection Kits for Cervical Cancer
What You Need to Know Before You Apply
What is the purpose of 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.
Who Is on the Research Team?
Michelle Silver, PhD, ScM
Principal Investigator
Washington University School of Medicine
Are You a Good Fit for This Trial?
Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Participants receive at-home HPV testing kits and complete a sociodemographic questionnaire. They receive either standard instructions or standard instructions with in-person guidance.
Follow-up
Participants are monitored for the return of HPV samples and participate in qualitative interviews to assess thematic findings related to capability, opportunity, motivation, and behavior.
What Are the Treatments Tested in This Trial?
Interventions
- HPV Self-Collection Kits
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Participants will complete a sociodemographic questionnaire and will receive the standard instructions and in-person navigation for registering for a consult to receive the at-home testing kit. After approximately 8 weeks, participants will be asked to participate in the qualitative interview.
Participants will complete a sociodemographic questionnaire and will receive the standard instructions. After approximately 8 weeks, participants will be asked to participate in the qualitative interview.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Washington University School of Medicine
Lead Sponsor
Teal Health, Inc.
Industry Sponsor
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