[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100630040":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":31,"locations":37,"responsibleParty":52,"collaborators":26,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":26,"eligibilityCriteria":62,"healthyVolunteers":58,"sex":63,"minAge":64,"maxAge":65,"enrollmentInfo":66,"targetDuration":26,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":77,"overallStatus":40,"whyStopped":26,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},{"fullName":5,"class":6},"Afyonkarahisar Health Sciences University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"First Group","EXPERIMENTAL","In addition to the neurological rehabilitation program (5 days per week, for 4 weeks totaling 20 sessions) repetitive transcranial magnetic stimulation (rTMS) will be applied using the MagVenture MagPro R30 device, with a Figure Eight Coil, according to the study protocol. rTMS will be delivered to the contralateral primary motor cortex (M1) upper extremity motor area at a low frequency of 1 Hz, with 5 sessions per week for 4 weeks, totaling 20 sessions.",[13],"Device: rTMS M1 Motor Cortex Protocol",{"label":15,"type":16,"description":17,"interventionNames":18},"Second Group","SHAM_COMPARATOR","Participants will receive the neurological rehabilitation program in the same form and dosage as applied in the active group. In addition, sham (placebo) repetitive transcranial magnetic stimulation (rTMS) will be administered to mimic the procedure without delivering active stimulation.",[19],"Device: Sham rTMS Protocol",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","rTMS M1 Motor Cortex Protocol","Repetitive transcranial magnetic stimulation (rTMS) will be applied using the MagVenture MagPro R30 device with a Figure Eight Coil according to the study protocol. rTMS will be delivered to the contralateral primary motor cortex (M1) upper extremity motor area at a low frequency of 1 Hz, 5 sessions per week for 4 weeks, totaling 20 sessions.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Sham rTMS Protocol","Sham (placebo) repetitive transcranial magnetic stimulation (rTMS) will be applied to mimic the procedure without delivering active stimulation. It was planned to apply it daily for 20 sessions.",[15],[32],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},"ülkü demir","CONTACT","5423541114","ulkudemir_44@hotmail.com",[38],{"facility":39,"status":40,"city":41,"state":26,"zip":42,"country":43,"countryCode":26,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"Afyonkarahisar Health Science University","RECRUITING","Afyonkarahisar","0300","Turkey (Türkiye)",{"type":45,"coordinates":46},"Point",[47,48],30.54333,38.75667,{"lat":48,"lon":47},[51],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},{"type":53,"investigatorFullName":54,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Nuran Eyvaz","Medical Doctor","100630040","repetitive-transcranial-magnetic-stimulation-in-cardiac-autonomic-dysfunction-100630040",false,"NCT07482501","Repetitive Transcranial Magnetic Stimulation in Cardiac Autonomic Dysfunction","The Effect of Repetitive Transcranial Magnetic Stimulation on Cardiac Autonomic Dysfunction in Patients With Stroke","Inclusion Criteria:\n\n* Participants aged 35-80 years admitted to the Afyonkarahisar Health Sciences University Hospital Physical Medicine and Rehabilitation Unit for neurological rehabilitation after stroke\n* Participants with a history of stroke of at least 3 months\n* Neurologically and medically stable participants willing to participate regularly in the study\n* Participants capable of following commands\n\nExclusion Criteria:\n\n* Serious cardiac disease, uncontrolled hypertension\n* Epilepsy or history of antiepileptic drug use\n* Intracranial metallic implants\n* Inner ear implants\n* Malignancy\n* Active infection\n* Skin infection or open wound in the intervention area\n* Brain lesions or medications that may alter the seizure threshold\n* Increased intracranial pressure\n* Uncontrolled migraine\n* Fracture or surgery on the hemiplegic side within the last 6 months\n* Pregnancy","ALL","35 Years","80 Years",{"count":67,"type":68},44,"ESTIMATED","INTERVENTIONAL",[71],"NA","The aim of this study is to investigate the effects of repetitive transcranial magnetic stimulation (rTMS) added to conventional neurological rehabilitation on heart rate variability (HRV), quality of life, upper extremity muscle strength and autonomic symptoms in patients with stroke.",[74,75,76],"Stroke","Autonomic Dysfunction","Hemiparesis",[78,79,80],"Repetitive Transcranial Magnetic Stimulation","Hemiplegia","Neurological Rehabilitation","2026-06-24",{"date":83,"type":84},"2026-06-25","ACTUAL",{"date":86,"type":84},"2026-03-26",{"date":88,"type":68},"2026-11-15",{"name":5,"class":6},1]