[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"exercises\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:exercises":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100574068","effects-of-upper-extremity-low-volume-hiit-in-heart-failure-100574068",false,"NCT06754475","Effects of Upper Extremity Low Volume HIIT in Heart Failure","The Effect of Upper Extremity Low-Volume High-Intensity Interval Training on Physical and Cognitive Functions in Heart Failure Patients","Inclusion Criteria:\n\n* Clinical condition stable for ≥4 weeks.\n* New York Heart Association functional classification I-II to III\n* Over 18 years old\n\nExclusion Criteria:\n\nHistory of CABG surgery\n\n* Unstable angina pectoris\n* Severe arrhythmia\n* Acute pericarditis, endocarditis, myocarditis\n* Severe left ventricular failure (EF \\\u003C40%)\n* Acute pulmonary embolism\n* History of syncope\n* Dissecting aneurysm\n* Thrombophlebitis\n* Orthopedic disorders that may interfere with exercise\n* Uncontrolled hypertension, severe pulmonary arterial hypertension\n* Moderate-severe valve disease\n* Decompensated Congestive Heart Failure\n* Electrolyte abnormalities\n* Hypertrophic Cardiomyopathy","ALL","18 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study was planned to investigate the effects of upper extremity low-volume high-intensity interval training (LV-HIIT) on physical and cognitive function in patients with heart failure with preserved ejection fraction(HFpEF).The research was planned as a randomized controlled trial. Patients with clinically stable HFpEF at cardiology clinic will be included in the study. These cases will be randomly divided into two groups: intervention group and control grup. After 8 weeks intervention physical functions before and after treatment; functional exercise capacity, arm exercise capacities , peripheral muscle strength , fatigue cognitive functions; anxiety and depression and fear of movement will be evaluated.",[26,27,28],"High Intensity Interval Training","Heart Failure","Exercises",[30,31,32],"high intensity interval training","upper extremity","exercises capacity","RECRUITING","2025-01-02",{"date":36,"type":37},"2025-01-03","ACTUAL",{"date":39,"type":37},"2024-11-01",{"date":41,"type":20},"2026-12-01",{"name":43,"class":44},"Tarsus University","OTHER",2]