[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100635920":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":11,"centralContacts":11,"locations":11,"responsibleParty":28,"collaborators":11,"id":30,"slug":31,"hasResults":32,"nctId":33,"briefTitle":34,"officialTitle":34,"acronym":11,"eligibilityCriteria":35,"healthyVolunteers":32,"sex":36,"minAge":37,"maxAge":38,"enrollmentInfo":39,"targetDuration":11,"studyType":42,"phases":43,"briefSummary":45,"conditions":46,"keywords":11,"overallStatus":48,"whyStopped":11,"lastUpdateSubmitDate":49,"lastUpdatePostDateStruct":50,"startDateStruct":53,"completionDateStruct":55,"leadSponsor":57,"locationsCount":11},{"fullName":5,"class":6},"The Children's Hospital of Zhejiang University School of Medicine","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Family-empowered pulmonary rehabilitation intervention group","EXPERIMENTAL",null,[13],"Behavioral: Family-empowered pulmonary rehabilitation",{"label":15,"type":6,"description":11,"interventionNames":16},"Conventional pulmonary rehabilitation care group",[17],"Behavioral: Conventional pulmonary rehabilitation care",[19,24],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":11},"BEHAVIORAL","Family-empowered pulmonary rehabilitation","Family-empowered pulmonary rehabilitation intervention, including education, skills training, and home-based rehabilitation guidance.",[9],{"type":20,"name":25,"description":26,"armGroupLabels":27,"otherNames":11},"Conventional pulmonary rehabilitation care","Routine pulmonary rehabilitation care and regular follow-up as per clinical practice.",[15],{"type":29,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100635920","application-construction-and-effect-evaluation-of-family-empowered-pulmonary-rehabilitation-in-school-age-children-with-asthma-100635920",false,"NCT07558954","Application Construction and Effect Evaluation of Family-empowered Pulmonary Rehabilitation in School-age Children With Asthma","Inclusion Criteria:(All must be met)\n\n* School-aged children aged 6 to 12 years.\n* Meet the diagnostic criteria for asthma according to the Guidelines for the Diagnosis and Prevention of Bronchial Asthma in Children (2025 Edition).\n* Received regular inhaled asthma medications for at least 3 months, with moderate or better medication adherence (score ≥6 on the Morisky Medication Adherence Scale).\n* Pulmonary function test shows obstructive ventilatory dysfunction or small airway dysfunction.\n* The primary caregiver has good communication and literacy skills, can use smartphone applications (e.g., WeChat) proficiently, and is willing to participate in the study.\n* Written informed consent has been obtained from the participant and their legal guardian.\n\nExclusion Criteria:(Any one leads to exclusion)\n\n* Children in acute asthma exacerbation.\n* Presence of other severe chronic diseases (e.g., congenital heart disease, neuromuscular disease, immunodeficiency disease, etc.).\n* Children with mental or psychological disorders who cannot cooperate.\n* Other conditions judged by the investigator to be unsuitable for participation in this study.","ALL","6 Years","12 Years",{"count":40,"type":41},92,"ESTIMATED","INTERVENTIONAL",[44],"NA","Study Purpose: To develop a pulmonary rehabilitation intervention program suitable for school-age children with asthma, and to evaluate its effectiveness in improving asthma control in children through a prospective randomized controlled trial.\n\nStudy Methods: This is a single-center, prospective, randomized, open-label, parallel-controlled trial. Eligible subjects who meet all inclusion criteria and none of the exclusion criteria, together with their families, will be randomly assigned in a 1:1 ratio to either the intervention group (family-empowered pulmonary rehabilitation intervention) or the control group (conventional pulmonary rehabilitation care) after signing the informed consent form.\n\nBoth groups will receive a 12-week core intervention period, with follow-up assessments conducted at baseline, end of intervention (12 weeks), and at 24 and 48 weeks after intervention.",[47],"Asthma Childhood","NOT_YET_RECRUITING","2026-04-26",{"date":51,"type":52},"2026-04-30","ACTUAL",{"date":54,"type":41},"2026-05-01",{"date":56,"type":41},"2027-12-31",{"name":5,"class":6}]