[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hr-hpv-testing\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hr-hpv-testing":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":5},"100580931","expanding-access-to-cervical-cancer-screening-through-primary-hr-hpv-testing-and-self-sampling-a-multicomponent-intervention-for-safety-net-health-systems-100580931",false,"NCT06843720","Expanding Access to Cervical Cancer Screening Through Primary HR-HPV Testing and Self-sampling: a Multicomponent Intervention for Safety Net Health Systems","Inclusion Criteria:\n\nPopulations involved in the research are:\n\n1. stakeholder advisory board members;\n2. patients eligible for cervical cancer screening participating in the cluster randomized stepped-wedge trial;\n3. patients and community members participating in formative research activities;\n4. providers, clinic staff, and other health system stakeholders from partnering health systems;\n5. Project ECHO Participants (providers, clinic staff, and other health system stakeholders from partner and non-partner institutions);\n6. Other Clinical Networks (providers, clinic staff and other health system stakeholders from partner and non-partner institutions)\n\nThe eligibility criteria for each are:\n\nPatients eligible for cervical cancer screening:\n\n* Currently a resident in the state of Texas\n* Attend for care at a partner clinic enrolled in the study\n* Women and persons with a cervix\n* Age 25-65\n* Due or past due for cervical cancer screening\n\nPatients and community members participating in formative research activities:\n\n• Purposively identified as a stakeholder for formative research by research staff\n\nProviders, clinic staff, and other health system stakeholders from partnering health systems:\n\n* Employed at least part-time by a partnering health system\n* Age 18+\n\nProject ECHO Participants:\n\n* Participate in at least one Project ECHO session\n* Age 18+\n\nOther Clinical Networks:\n\n* Participate in at least one clinical network session\n* Age 18+\n\nExclusion Criteria:\n\nPatients eligible for cervical cancer screening:\n\n* Report being currently pregnant\n* History of total hysterectomy\n* History of cervical cancer\n\nOther study populations:\n\n• Unable to communicate in English or Spanish\n\nVulnerable Populations Participants\u002Fsamples belonging to vulnerable populations (children, pregnant women, cognitively impaired adults, or prisoners) will be prohibited from participation.",true,"FEMALE","18 Years","65 Years",{"count":20,"type":21},7100,"ESTIMATED","INTERVENTIONAL",[24],"NA","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.",[27],"HR-HPV Testing","RECRUITING","2026-06-22",{"date":31,"type":32},"2026-06-23","ACTUAL",{"date":34,"type":32},"2025-02-17",{"date":36,"type":21},"2031-03-31",{"name":38,"class":39},"M.D. Anderson Cancer Center","OTHER"]