[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"telemedicine-based-education\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:telemedicine-based-education":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,52],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100633373","a-pragmatic-clinical-trial-of-the-we-beat-well-being-education-program-in-adolescent-congenital-heart-disease-we-beat-chd-study-100633373",false,"NCT07525843","A Pragmatic Clinical Trial of the WE BEAT Well-Being Education Program in Adolescent Congenital Heart Disease: WE BEAT CHD Study","PHN WBC","Inclusion Criteria:\n\n* Age 12-17 years old\n* CHD of moderate or severe complexity (Class II\u002FIII, 2018 AHA\u002FACC ACHD, Table 4)\n* English or Spanish language proficiency\n* Receives cardiology care at a PHN or PHN auxiliary site\n* Parent or guardian and participant willing to comply with protocol and provide written\u002Felectronic informed consent and assent\n\nExclusion Criteria:\n\n* CHD of mild or simple complexity (Class I, 2018 AHA\u002FACC ACHD, Table 4)\n* Prior heart transplant to treat CHD\n* Heart disease that is not classified as structural CHD (e.g., connective tissue disease, genetic cardiomyopathy, or acquired heart disease)\n* Cognitive or developmental conditions that limit program participation and\u002For ability to complete self-reported measures as determined by a primary cardiology clinician\n* Suicidality, homicidality, or psychosis in the past 12 months as per medical chart review, clinician report, or eligibility screening\n* Medically unable to participate (e.g., intubated, unable to respond verbally, active delirium)","ALL","12 Years","17 Years",{"count":20,"type":21},390,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this pragmatic clinical trial is to learn if the WE BEAT program, a 5-week group-based online wellbeing and skill-building program, can help teens with congenital heart disease (CHD) improve their ability to handle stress. The main question it aims to answer is if participants who receive the WE BEAT program become more resilient (the ability to bounce back from from tough times or recover from something difficult) and have better quality of life compared to participants who receive usual care. The study also aims to learn if there are connections between participant-reported psychosocial data (such as resilience, feelings about one's life and one's physical, mental, and social wellbeing) and clinical outcomes.\n\nEligible participants who are 12-17-year-old will be in the study for about 6 months and be randomized to receive either the WE BEAT program or usual care. Following completion of the primary WE BEAT intervention at Week 5, intervention arm participants will be randomized to a single-session booster session (occurring at Week 18) vs no booster session. The booster session will be provided in a similar format to the WE BEAT program. A review of all modules\u002Fskills introduced in the program will be provided.\n\nAll participants will complete 4 sets of online surveys and give 3 hair\u002Fsaliva samples at different timepoints. Some participants may volunteer to give optional blood and urine samples.",[27,28,29,30,31,32],"Patient-Reported Outcome Measures (PROMs)","Pragmatic Trial","Adolescent Congenital Heart Disease","Resiliency-building Intervention","Resilience, Psychological","Telemedicine-Based Education",[34,35,36,37,38],"WE BEAT","Well-Being Education Program","Adolescent CHD","Pragmatic Clinical Trial","Telemedicine","RECRUITING","2026-06-18",{"date":42,"type":43},"2026-06-22","ACTUAL",{"date":45,"type":43},"2026-04-20",{"date":47,"type":21},"2029-06",{"name":49,"class":50},"Carelon Research","OTHER",14,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":16,"minAge":60,"maxAge":61,"enrollmentInfo":62,"targetDuration":4,"studyType":22,"phases":64,"briefSummary":65,"conditions":66,"keywords":68,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":81},"100573971","telemedicine-education-for-caregivers-and-asthma-control-in-children-100573971","NCT06753214","Telemedicine Education for Caregivers and Asthma Control in Children","Effectiveness of Telemedicine-Based Education for Caregivers on Asthma Control in Children With Uncontrolled Asthma: A Randomized Controlled Trial","TCARE","Inclusion Criteria:\n\n* Pediatric asthma patients diagnosed according to the GINA guidelines, classified as having uncontrolled asthma, are managed and followed up for at least 1 month at the pediatric asthma unit of the outpatient department.\n\nExclusion Criteria:\n\n* Pediatric patients who do not cooperate or are unable to complete the Childhood Asthma Control Test questionnaire.\n* Caregivers who cannot complete the questionnaires related to the assessment of asthma control and associated factors.\n* Pediatric patients who have siblings participating in the study.\n* Patients currently participating in another clinical study (excluding non-interventional studies or registries).\n* Failure to return for a second visit within 6 months following enrollment.","4 Years","16 Years",{"count":63,"type":21},64,[24],"Asthma control in pediatric patients remains a critical issue for healthcare providers. Telemedicine has emerged as an effective solution for overcoming distance barriers in healthcare delivery. This study aims to utilize telemedicine-based education for caregivers to improve asthma control in children with uncontrolled asthma. By providing remote guidance and support, the study seeks to enhance caregivers' knowledge and management practices, ultimately leading to better asthma outcomes for pediatric patients.",[67,32],"Uncontrolled Asthma",[69,70,38,71],"Asthma","Pediatrics","Uncontrolled asthma","2025-07-02",{"date":74,"type":43},"2025-07-08",{"date":76,"type":43},"2024-06-05",{"date":78,"type":21},"2026-06",{"name":80,"class":50},"Can Tho University of Medicine and Pharmacy",1]