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Recruiting Not applicable NCT07453459

Feasibility of HPV Self-Collection Kits for Cervical Cancer Screening

No applicable phase (e.g. observational)
Conditions: Cervical Cancer HPV Infection

Sponsor: Washington University School of Medicine

trial.available_in: БГ
Overview
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 can participate
Inclusion Criteria: * Are age 25-65 * Has an intact cervix * Self-reports that they have not been screened for cervical cancer within the last 3 years * Has a smartphone * Has access to the internet to engage with 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 Exclusion Criteria: * Abnormal vaginal bleeding or discharge * A history of cancer of the reproductive system * A compromised immune system * Prior Diethylstilbestrol (DES) exposure * Currently pregnant or are within 6 weeks of giving birth * Treatment for a cervical precancer (e.g., loop electrosurgical excision procedure or conization) in the last 25 years.
Interventions
Qualitative Interview
BEHAVIORAL
Virtual Visit Standard Instructions
BEHAVIORAL
Virtual Visit Standard Instructions + In-Person Registration Navigation
BEHAVIORAL
Locations 1
United States (1)
Washington University School of Medicine
St Louis , Missouri
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Female only
Minimum age
25 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
17.04.2026
Completion date
15.01.2028
Registry ID
NCT07453459
Source
clinicaltrials.gov
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