[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100577620":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":27,"centralContacts":37,"locations":45,"responsibleParty":61,"collaborators":64,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":74,"eligibilityCriteria":75,"healthyVolunteers":70,"sex":76,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":19,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":19,"overallStatus":47,"whyStopped":19,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":102},{"fullName":5,"class":6},"Baylor University","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention Group","EXPERIMENTAL","Health providers and management at IG sites will receive ISS (i.e., management support, capacity-building, and social network support) and training on the HOPE implementation plan",[13,14],"Behavioral: Health providers and management at IG sites will receive ISS (i.e., management support, capacity-building, and social network support) and training on the HOPE implementation plan","Behavioral: Control Group",{"label":16,"type":17,"description":18,"interventionNames":19},"Control Group","NO_INTERVENTION","Providers and management in the control group will not receive any ISS or implementation plan training",null,[21,24],{"type":22,"name":11,"description":11,"armGroupLabels":23,"otherNames":19},"BEHAVIORAL",[9],{"type":22,"name":16,"description":25,"armGroupLabels":26,"otherNames":19},"Providers in the control group will not receive ISS support",[9],[28,31,34],{"name":29,"affiliation":5,"role":30},"Matthew Asare, PhD","PRINCIPAL_INVESTIGATOR",{"name":32,"affiliation":33,"role":30},"Dorcas Obiri-Yeboah, PhD","University of Cape Coast",{"name":35,"affiliation":36,"role":30},"Nadia Sam-Agudu, MD","University of Minnesota",[38,42],{"name":29,"role":39,"phone":40,"phoneExt":19,"email":41},"CONTACT","5136416482","Matt_asare@baylor.edu",{"name":32,"role":39,"phone":43,"phoneExt":19,"email":44},"233+244-527387","dobiri-yeboah@ucc.edu.gh",[46],{"facility":33,"status":47,"city":48,"state":49,"zip":19,"country":50,"countryCode":51,"cosmosGeoPoint":52,"geoPoint":57,"contacts":58},"RECRUITING","Cape Coast","Central Region","Ghana","GH",{"type":53,"coordinates":54},"Point",[55,56],-1.2466,5.10535,{"lat":56,"lon":55},[59],{"name":32,"role":39,"phone":60,"phoneExt":19,"email":44},"+233244-527387",{"type":30,"investigatorFullName":62,"investigatorTitle":63,"investigatorAffiliation":5,"oldNameTitle":19,"oldOrganization":19},"Matt Asare","Assistant Professor",[65],{"name":66,"class":67},"National Cancer Institute (NCI)","NIH","100577620","home-based-self-sampling-for-cervical-cancer-prevention-education-intervention-in-ghana-100577620",false,"NCT06800664","Home-based Self-sampling for Cervical Cancer Prevention Education Intervention in Ghana","The Impact of an Evidence-Based, Behavioral Cervical Cancer Screening Intervention Among Women Living With HIV in Ghana (HOPE-inG): A Type 2 Hybrid Effectiveness Implementation Trial","HOPE-inG","Inclusion Criteria:\n\nGeneral criteria\n\n* ability to give consent per Institutional Review Board stipulations\n* residing in the Central Region\n* having no medical characteristics that would interfere with the ability to participate fully\n* the willingness to participate in this study.\n\n  (a) Healthcare provider eligibility: Inclusion criteria include an individual (no gender restrictions) who\n* possesses healthcare qualifications (i.e., patient navigators, physicians, nurses, health facility management),\n* works at the HIV health facility at study sites,\n* is ≥18 years old. (b) Eligibility for women living with HIV (Patients)\n* identified female at birth) who\n* are living with HIV between 25 and 65 years old (age consistent with WHO CC screening guidelines)\n* have never had CC screening (Pap or HPV test),\n* have not had a screening for the past 5 years\n\nExclusion Criteria:\n\n* Women will be excluded if they are pregnant or have had a hysterectomy.\n* WLWH who have a cervix are the main target population to develop the HOPE toolkit.\n* Women who are below 25 and those who are above 65 years will be excluded.","ALL","25 Years","65 Years",{"count":80,"type":81},1500,"ESTIMATED","INTERVENTIONAL",[84],"NA","The investigators propose to develop and\u002For adapt implementation strategies and a structured implementation plan to translate the HOPE intervention into existing healthcare practice in Ghana.\n\nThese \"implementation support strategies (ISS)\" are implementation strategies relevant to implementation support, which is concerned with moving (implementation) research into (implementation) practice.\n\nThe ultimate goal is to facilitate health system adoption and sustainment.",[87,88,89,90,91,92],"Cervical Cancer Screening","HIV","Self-sampling","Implementation Science","Intervention (Training) Condition","Implementation Strategies","2026-06-30",{"date":95,"type":96},"2026-07-01","ACTUAL",{"date":98,"type":96},"2025-11-11",{"date":100,"type":81},"2029-05",{"name":5,"class":6},1]