[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100627315":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":39,"centralContacts":51,"locations":58,"responsibleParty":72,"collaborators":27,"id":76,"slug":77,"hasResults":78,"nctId":79,"briefTitle":80,"officialTitle":80,"acronym":27,"eligibilityCriteria":81,"healthyVolunteers":78,"sex":82,"minAge":83,"maxAge":84,"enrollmentInfo":85,"targetDuration":27,"studyType":88,"phases":89,"briefSummary":91,"conditions":92,"keywords":27,"overallStatus":94,"whyStopped":27,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},{"fullName":5,"class":6},"Cairo University","OTHER",[8,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Aerobic training + Inspiratory muscle training + Cognitive training + Conventional therapy","EXPERIMENTAL","Twenty patients will receive a comprehensive intervention program consisting of aerobic training, inspiratory muscle training, and cognitive training in addition to conventional therapy. The intervention will be implemented throughout the hospitalization period and will continue for a minimum duration of three weeks.",[13,14,15,16],"Other: Aerobic training","Other: Inspiratory muscle training","Other: Cognitive training","Other: Conventional therapy",{"label":18,"type":19,"description":20,"interventionNames":21},"Conventional therapy","ACTIVE_COMPARATOR","Twenty patients will receive conventional therapy only. The intervention will be implemented throughout the hospitalization period and will continue for a minimum duration of three weeks.",[16],[23,28,32,36],{"type":6,"name":24,"description":25,"armGroupLabels":26,"otherNames":27},"Aerobic training","Participants in the experimental group will receive arm ergometer training performed at the bedside for 10-15 minutes, twice daily, at low-to-moderate intensity corresponding to 40-50% of the age-predicted maximum heart rate, under appropriate monitoring. The intervention will be continued throughout the hospitalization period for a minimum duration of three weeks.",[9],null,{"type":6,"name":29,"description":30,"armGroupLabels":31,"otherNames":27},"Inspiratory muscle training","Participants in the experimental group will receive inspiratory muscle training using a threshold device set at 30% of maximal inspiratory pressure, performed twice daily for 15 minutes per session. The training load will be progressively increased according to patient tolerance, and the intervention will be continued throughout the hospitalization period for a minimum duration of three weeks.",[9],{"type":6,"name":33,"description":34,"armGroupLabels":35,"otherNames":27},"Cognitive training","Participants in the experimental group will receive computerized cognitive training consisting of 20-minute daily sessions targeting attention, memory, and problem-solving abilities. The intervention will be implemented throughout the hospitalization period and will continue for a minimum duration of three weeks.",[9],{"type":6,"name":18,"description":37,"armGroupLabels":38,"otherNames":27},"Participants in both groups will receive conventional therapy. The intervention will be implemented throughout the hospitalization period and will continue for a minimum duration of three weeks.",[9,18],[40,44,48],{"name":41,"affiliation":42,"role":43},"Azza Abdel Aziz, PhD","Ass. Professor, Cairo University","STUDY_CHAIR",{"name":45,"affiliation":46,"role":47},"Alaa Mohamed Naguib, PhD","Lecturer, Cairo University","STUDY_DIRECTOR",{"name":49,"affiliation":50,"role":47},"Ahmed Mohamed Abdelmegeed ElFeky","Lecturer, Misr University for science and technology",[52,57],{"name":53,"role":54,"phone":55,"phoneExt":27,"email":56},"Hajar Suleiman Zakaria, B.Sc","CONTACT","+20 10 69177694","Hajar.afifi@must.edu.eg",{"name":45,"role":54,"phone":27,"phoneExt":27,"email":27},[59],{"facility":60,"status":27,"city":61,"state":27,"zip":27,"country":62,"countryCode":63,"cosmosGeoPoint":64,"geoPoint":69,"contacts":70},"Cardiology department at El-Kasr El Einy University hospital","Giza","Egypt","EG",{"type":65,"coordinates":66},"Point",[67,68],31.20861,30.00944,{"lat":68,"lon":67},[71],{"name":53,"role":54,"phone":55,"phoneExt":27,"email":56},{"type":73,"investigatorFullName":74,"investigatorTitle":75,"investigatorAffiliation":5,"oldNameTitle":27,"oldOrganization":27},"PRINCIPAL_INVESTIGATOR","Hajar Suleiman Zakaria","Principal investigator","100627315","integrating-aerobic-respiratory-and-cognitive-training-in-acute-heart-failure-100627315",false,"NCT07447037","Integrating Aerobic, Respiratory, and Cognitive Training in Acute Heart Failure","Inclusion Criteria:\n\n* Age between 50-65 years.\n* All patients are male.\n* Diagnosed with acute heart failure according to ESC guidelines.\n* Hemodynamically stable for at least 24 hours.\n* Able to follow simple verbal commands and participate in training.\n\nExclusion Criteria:\n\n* Unstable angina or recent myocardial infarction (\\\u003C 4 weeks).\n* Severe uncontrolled arrhythmias or advanced atrioventricular block.\n* Severe pulmonary disease (e.g., advanced COPD, restrictive lung disease).\n* Neurological disorders causing cognitive or motor disability.\n* Orthopedic or musculoskeletal conditions preventing upper-limb activity.\n* Severe visual or auditory impairment limiting participation in cognitive training.","FEMALE","50 Years","65 Years",{"count":86,"type":87},40,"ESTIMATED","INTERVENTIONAL",[90],"NA","The purpose of this study is to investigate the impact of integrating aerobic, respiratory and cognitive training in acute heart failure.",[93],"Acute Heart Failure","NOT_YET_RECRUITING","2026-02-26",{"date":97,"type":98},"2026-03-03","ACTUAL",{"date":100,"type":87},"2026-03-07",{"date":102,"type":87},"2026-04-30",{"name":5,"class":6},1]