[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Erol Olcok Corum Training and Research Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":98},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,75],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100640844","comparison-of-the-effects-of-different-upper-extremity-aerobic-exercise-training-protocols-on-arm-functional-capacity-in-patients-with-heart-failure-with-cardiac-implantable-electronic-devices-100640844",false,"NCT07592494","Comparison of the Effects of Different Upper Extremity Aerobic Exercise Training Protocols on Arm Functional Capacity in Patients With Heart Failure With Cardiac Implantable Electronic Devices","Inclusion Criteria:\n\n* Patients aged 18 and over with heart failure who are receiving Implantable Cardioverter Defibrillator (ICD) or Cardiac Resynchronization Therapy (CRT)\n* At least 3 months have passed since device implantation and there have been no complications at the last device control\n* Being in New York Heart Association (NYHA) Class II-III\n* Patients without cooperation problems\n* Patients who volunteer to participate in the study\n\nExclusion Criteria:\n\n* Patients who have previously participated in a cardiac rehabilitation program and those who have completed less than 1 year since the program,\n* Patients with a primary diagnosis of cardiomyopathy and those with heart failure secondary to cardiomyopathy,\n* Patients with a history of shoulder pathologies that may restrict upper extremity movement before device implantation (such as severe pain around the shoulder, edema, or shoulder dislocation that restricts upper extremity movement),\n* Patients with a history of shoulder surgery (patients with limitations in range of motion),\n* Patients who have undergone mastectomy on the affected side or a cerebrovascular event resulting in arm involvement,\n* Patients with decompensated heart failure,\n* Patients with a history of ICD-incompatible shock,\n* Patients with a history of unstable angina pectoris, acute myocardial infarction, or cardiac surgery within the last 3 months,\n* Patients who have experienced acute atrial fibrillation, ventricular tachycardia, and ventricular fibrillation within the last 3 months,\n* Patients with actively treated malignancy or collagen tissue disease receiving systemic steroids\n* Patients with chronic kidney disease undergoing dialysis where volume load is unstable,\n* Persistent ventricular arrhythmias during baseline cardiopulmonary exercise testing.","ALL","18 Years",{"count":18,"type":19},36,"ESTIMATED","INTERVENTIONAL",[22],"NA","1. To determine the most suitable exercise protocol for upper extremity aerobic exercise training, a widely used type of aerobic exercise to improve reduced upper extremity functional capacity in individuals with CIED and HF.\n2. To investigate whether high-intensity intermittent upper extremity aerobic exercise training provides a more effective improvement in upper extremity functional capacity compared to moderate-intensity continuous upper extremity aerobic exercise training.\n3. To determine the effectiveness of different types of upper extremity aerobic exercise training compared to lower extremity aerobic training alone in individuals with CIED and HF.",[25,26,27],"Heart Failure","Implantable Cardioverter Defibrillator (ICD)","Cardiac Resynchronization Therapy Devices",[29,30,25,31,32,33],"Implantable Cardioverter Defibrillator","Cardiac Resynchronization Therapy Device","Upper Extremity Aerobic Exercise","Cardiac Rehabilitation","Physiotherapy and Rehabilitation","NOT_YET_RECRUITING","2026-05-11",{"date":37,"type":38},"2026-05-18","ACTUAL",{"date":35,"type":19},{"date":41,"type":19},"2027-05-11",{"name":43,"class":44},"Erol Olcok Corum Training and Research Hospital","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":53,"targetDuration":55,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},"100625242","seasonal-physical-activity-in-patients-with-heart-failure-with-cardiac-implantable-electronic-devices-100625242","NCT07420088","Seasonal Physical Activity in Patients With Heart Failure With Cardiac Implantable Electronic Devices","The Effect of Seasonal Variation on Physical Activity in Patients With Heart Failure With Cardiac Implantable Electronic Devices","CIED","Inclusion Criteria:\n\n* Over 18 years of age,\n* Have a diagnosis of heart failure due to ischemic or non-ischemic cardiomyopathy,\n* Have a cardiac implantable electrical devices,\n* Be in New York Heart Association (NYHA) Class I-II-III.\n\nExclusion Criteria:\n\n* Being a New York Heart Association (NYHA) Class IV resident\n* Not living within a 50-mile radius of a weather reporting station,\n* Having documented conditions that limit ambulation, including wheelchair use, serious orthopedic problems, stroke and other neurological disorders, or amputation,\n* Using a left ventricular assist device,\n* Having a history of more than five hospitalizations for any reason,\n* Having recently undergone major cardiovascular or orthopedic surgical procedures, including coronary artery bypass grafting, aortic aneurysm repair, joint replacement, amputation, or spinal surgery,\n* Having a cognitive impairment that impairs cooperation with questionnaires or tests.",{"count":54,"type":19},24,"12 Months","OBSERVATIONAL","The aim of this observational study is to determine the effect of seasonal changes on physical activity levels in heart failure patients with cardiac implantable electronic devices.\n\nPatients with heart failure who have a cardiac implantable electronic device will be evaluated throughout the year.",[25,59,60],"Cardiac Implantable Electrical Devices","Physical Activities",[62,63,64],"Cardiac implantable electronic device","physical activity","seasonal variation","RECRUITING","2026-05-05",{"date":68,"type":38},"2026-05-08",{"date":70,"type":38},"2026-01-21",{"date":72,"type":19},"2027-01-21",{"name":43,"class":44},1,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":92,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":74},"100575664","assessment-of-validity-and-reliability-of-the-turkish-version-of-the-quality-of-life-and-related-events-assessment-scale-for-pacemaker-patients-100575664","NCT06775223","Assessment of Validity and Reliability of the Turkish Version of the Quality of Life and Related Events Assessment Scale for Pacemaker Patients","Inclusion Criteria:\n\n* Having a pacemaker implant and not having any complications at the last pacemaker check-up,\n\n  * Being in NYHA I-II-III-IV class,\n  * Patients with no cooperation problems,\n  * Volunteering to participate in the study.\n\nExclusion Criteria:\n\n* • Patients with insufficient dementia or cognitive impairment due to multiple comorbidities (e.g., recent cerebrovascular accident and\u002For significant hypotension),\n\n  * Patients with a history of psychiatric illness,\n  * Patients with speech, hearing or intellectual disabilities.","65 Years",{"count":83,"type":19},120,"Cardiac implantable electronic devices are widely utilized to lower the rates of morbidity and mortality from ventricular tachycardia and ventricular fibrillation, as well as the incidence of sudden cardiac death. Although implantation of these devices increases survival rates, patients may experience acute and chronic complications. These complications include device dislocation and fracture, inappropriate shocks, pocket hematoma, or infection. Furthermore, functional loss in the upper extremity may result from upper extremity restrictions that are applied for an excessively long time in order to ensure proper placement of the device following implantation, or from patients who choose to extend this period on their own initiative out of worry about device failure or dislocation. Patients' quality of life may be negatively impacted by these issues as well as diminished exercise capacity, weariness, and weaker respiratory and peripheral muscles. A quality of life scale called 'The Assessment of Quality of Life and Related Events (AQUAREL)' was developed by Stoffmel et al. for patients using pacemakers. In this study, the validity and reliability study of the Turkish version of the AQAREL Scale will be conducted.",[86,87],"Cardiac Implantable Electronic Devices","Quality of Life",[89,90,91],"quality of life","patient reported outcomes","cardiac implantable electronic devices",{"date":68,"type":38},{"date":94,"type":38},"2024-06-05",{"date":96,"type":19},"2026-06-01",{"name":43,"class":44},""]