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Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems
RecruitingHealthy volunteers welcome
Who can join
Ages 18 to 65 · Women · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: Populations involved in the research are: 1. stakeholder advisory board members; 2. patients eligible for cervical cancer screening participating in the cluster randomized stepped-wedge trial; 3. patients and community members participating in formative research activities; 4. providers, clinic staff, and other health system stakeholders from partnering health systems; 5. Project ECHO Participants (providers, clinic staff, and other health system stakeholders from partner and non-partner institutions); 6. Other Clinical Networks (providers, clinic staff and other health system stakeholders from partner and non-partner institutions) The eligibility criteria for each are: Patients eligible for cervical cancer screening: * Currently a resident in the state of Texas * Attend for care at a partner clinic enrolled in the study * Women and persons with a cervix * Age 25-65 * Due or past due for cervical cancer screening Patients and community members participating in formative research activities: • Purposively identified as a stakeholder for formative research by research staff Providers, clinic staff, and other health system stakeholders from partnering health systems: * Employed at least part-time by a partnering health system * Age 18+ Project ECHO Participants: * Participate in at least one Project ECHO session * Age 18+ Other Clinical Networks: * Participate in at least one clinical network session * Age 18+ Exclusion Criteria: Patients eligible for cervical cancer screening: * Report being currently pregnant * History of total hysterectomy * History of cervical cancer Other study populations: • Unable to communicate in English or Spanish Vulnerable Populations Participants/samples belonging to vulnerable populations (children, pregnant women, cognitively impaired adults, or prisoners) will be prohibited from participation.
About the study
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.
What is being tested
- HR-HPV Testing (behavioral)
Sponsor: M.D. Anderson Cancer Center · Participants: 7,100 · Started: Feb 17, 2025
Contact the study team
- Jane R Montealegre, PHD · Phone: 713- 745-5008
Official record on ClinicalTrials.gov — NCT06843720
Locations in the U.S.
| Texas | MD Anderson Cancer Center, Houston |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.