[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"QVITI S.A.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":44},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":4,"eligibilityCriteria":13,"healthyVolunteers":10,"sex":14,"minAge":15,"maxAge":16,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100454209",false,"NCT05194566","Neurostimulation for the Treatment of Post-Stroke Aphasia","Individuals with aphasia (assessed using the Boston Diagnostic Aphasia Examination) who perform the Naming Task in the range of 10%-60% accuracy will be included in the study. The overall baseline score in the Naming Task will be estimated from the two baseline measurements.\n\nInclusion Criteria:\n\n* diagnosis of aphasia: Broca's or mixed (based on the assessment of a Speech Language Pathologist).\n* presence of a focus of injury in the left hemisphere (within one hemisphere only) as a result of the first ischemic or hemorrhagic stroke (based on CT\u002FMRI examination);\n* chronic stage of the disease - time since the stroke occurred over 6 months.\n* ability to achieve an accuracy in the Naming Task of 10-60%.\n* 18-80 years\n* right-handedness before the stroke.\n* ability to give informed written consent.\n* fluency in English.\n\nExclusion Criteria:\n\n* severe cognitive, auditory or visual impairment that would preclude cognitive and language testing - inability to follow a two-step command.\n* presence of metal implants in the skull.\n* presence of major untreated or unstable psychiatric disease.\n* history of epilepsy or seizures.\n* ongoing medication that increases the risk of epileptic seizures.\n* presence in the body of cardiac stimulator, pacemaker or vagus nerve stimulator (implanted).\n* history of speech, language, hearing, or intellectual disability during childhood.\n* pregnancy (based on declarations)\n\nExclusion criteria during the trial:\n\n* high intolerance to stimulation.\n* occurrence of an epileptic seizure.\n* other previously absent neurological or mental symptoms\n\nWithdrawal criteria:\n\n* high intolerance to stimulation (participants experience severe discomfort during stimulation);\n* occurrence of an epileptic seizure;\n* other previously absent neurological, physical or mental symptoms.","ALL","18 Years","80 Years",{"count":18,"type":19},64,"ESTIMATED","INTERVENTIONAL",[22],"NA","The aim of the trial is to determine whether 75Hz transcranial alternating current stimulation (tACS) synchronized with therapeutic linguistic tasks is an effective form of therapy for post-stroke aphasia.",[25],"Post-stroke Aphasia",[27,28,29,30],"speech therapy","brain stimulation","communication","language","RECRUITING","2026-02-13",{"date":34,"type":35},"2026-02-18","ACTUAL",{"date":37,"type":35},"2023-09-06",{"date":39,"type":19},"2026-12",{"name":41,"class":42},"QVITI S.A.","INDUSTRY",2,""]