Actively Recruiting
Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems
Led by M.D. Anderson Cancer Center · Updated on 2026-02-27
7100
Participants Needed
1
Research Sites
319 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To learn about the attitudes toward implementing self-collection among healthcare providers and staff, participants, and other stakeholders; and to inform the development of patient education and provider training materials to aid in the implementation of self-collection in clinical settings.
CONDITIONS
Official Title
Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant is currently a resident of Texas
- Participant attends care at a partner clinic enrolled in the study
- Participant is female or a person with a cervix
- Participant is aged 25 to 65 years
- Participant is due or past due for cervical cancer screening
- Stakeholder advisory board members are eligible
- Participants eligible for cervical cancer screening in the cluster randomized stepped-wedge trial
- Patients and community members involved in formative research activities
- Providers, clinic staff, and other health system stakeholders employed at least part-time by a partnering health system and aged 18 or older
- Project ECHO participants who attend at least one session and are aged 18 or older
- Participants in other clinical networks who attend at least one session and are aged 18 or older
You will not qualify if you...
- Currently pregnant individuals
- History of total hysterectomy
- History of cervical cancer
- Individuals unable to communicate in English or Spanish
- Members of vulnerable populations including children, pregnant women, cognitively impaired adults, or prisoners are excluded
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
MD Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
J
Jane R Montealegre, PHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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