[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100604142":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":23,"locations":32,"responsibleParty":50,"collaborators":54,"id":61,"slug":62,"hasResults":63,"nctId":64,"briefTitle":65,"officialTitle":66,"acronym":67,"eligibilityCriteria":68,"healthyVolunteers":69,"sex":70,"minAge":71,"maxAge":72,"enrollmentInfo":73,"targetDuration":18,"studyType":76,"phases":77,"briefSummary":79,"conditions":80,"keywords":84,"overallStatus":35,"whyStopped":18,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":98},{"fullName":5,"class":6},"Universiteit Antwerpen","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Transition program","EXPERIMENTAL","A transition program (TP) was developed, as part of the first work package of the COCCOS project, in close collaboration with stakeholders (i.e., AYA patients, parents and HCPs) based on participatory action research methods (i.e., Experience-Based Co Design, including photovoice). Based on this study, the developed TP entailed four key moments: (i) a transition consultation, (ii) a consultation without parents, (iii) a joint consultation, and (iv) a feedback moment. Over a course of approximately 9-15 months (this can differ considering different pathologies have different care trajectories (e.g., frequency of consultations)), AYAs will receive an intensive person-centered transition program consisting of the four key moments.",[13],"Other: Transition program",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard care","NO_INTERVENTION","Participants in this arm will receive standard of care.",null,[20],{"type":6,"name":9,"description":21,"armGroupLabels":22,"otherNames":18},"Transition Consultation:\n\nPediatric HCP introduces the transition process to AYA and family. A contact person is assigned (ideally the AYA's trusted HCP), along with someone from the AYA's personal network. Key points are recorded in the Individualized Transition Plan (ITP).\n\nIndependent Visit:\n\nAYA has a solo consultation (parents briefly step out). They complete the Ready Steady Go checklist. The ITP is updated, and concerns are discussed.\n\nJoint Consultation:\n\nPediatric and adult HCPs meet with the AYA. A new adult contact is assigned, and the AYA picks a pediatric contact for feedback. Checklist is completed again.\n\nFeedback Moment:\n\nAfter transfer, the pediatric contact checks in. The checklist guides discussion; feedback is shared across teams, and follow-up arranged if needed.",[9],[24,29],{"name":25,"role":26,"phone":27,"phoneExt":18,"email":28},"Eva Goossens, Professor","CONTACT","+32472722364","eva.goossens@uantwerpen.be",{"name":30,"role":26,"phone":18,"phoneExt":18,"email":31},"Natwarin Janssens","natwarin.janssens@ugent.be",[33],{"facility":34,"status":35,"city":36,"state":18,"zip":37,"country":38,"countryCode":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":46},"Ghent University Hospital","RECRUITING","Ghent","9000","Belgium","BE",{"type":41,"coordinates":42},"Point",[43,44],3.71667,51.05,{"lat":44,"lon":43},[47],{"name":30,"role":26,"phone":48,"phoneExt":18,"email":49},"0471840273","Natwarin.Janssens@UGent.be",{"type":51,"investigatorFullName":52,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Eva Goossens","professor",[55,57,59],{"name":56,"class":6},"University Ghent",{"name":58,"class":6},"University Hospital, Ghent",{"name":60,"class":6},"University Hospital, Antwerp","100604142","the-coccos-study-a-transition-program-for-young-persons-with-chronic-conditions-100604142",false,"NCT07145671","The COCCOS Study: a Transition Program for Young Persons With Chronic Conditions","The COCCOS Study: Implementing and Evaluating a Transition Program for Young Persons With Chronic Conditions","COCCOS","Inclusion criteria:\n\nFor participants in the intervention group (IG):\n\n* 17 years old;\n* diagnosed with type 1 diabetes, asthma and\u002For obesity;\n* who had at least one pediatric outpatient visit, prior to inclusion, in one of both hospitals within the past 12 months;\n* are Dutch speaking;\n* planned to transfer to adult care within the next 12 months.\n\nFor participants in the control group (CG):\n\n* age 17,5 and 18 years old, as the control period has a shorter duration (4 months vs. 12 months)\n* diagnosed with type 1 diabetes, asthma and\u002For obesity;\n* who had at least one pediatric outpatient visit, prior to inclusion, in one of both hospitals within the past 12 months;\n* are Dutch speaking;\n* planned to transfer to adult care within the next 12 months.\n\nExclusion criteria:\n\nApplicable for both CG and IG:\n\n\\- patients with severe mental, cognitive or neurological problems will be excluded",true,"ALL","16 Years","21 Years",{"count":74,"type":75},150,"ESTIMATED","INTERVENTIONAL",[78],"NA","A study is undertaken to examine the feasibility of the newly developed transition program in adolescents with type 1 diabetes, asthma and obesity in a multicentric setting. Specific objectives for this study are: (1) examining the impact of the program in terms of patient-reported health outcomes, (2) examining patients' and healthcare providers' experiences related to the program implementation process, and (3) examining the impact of the program in terms of cost-effectiveness.",[81,82,83],"Type 1 Diabetes Mellitus","Obesity","Asthma",[85,86,87,88],"adolescent","young adult","transitional care","transition program","2025-08-20",{"date":91,"type":92},"2025-08-28","ACTUAL",{"date":94,"type":92},"2025-03-13",{"date":96,"type":75},"2026-12",{"name":5,"class":6},1]