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NCT06843720
Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems
Conditions: HR-HPV Testing
Sex: Female
Ages: 18 Years – 65 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 7100
Sponsor: M.D. Anderson Cancer Center
Location: MD Anderson Cancer Center Houston Texas
Summary
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.
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.
Source: ClinicalTrials.gov (NCT06843720). StuddyBuddy aggregates publicly available trial information.