[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University Rehabilitation Institute, Republic of Slovenia\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":194},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,48,75,101,125,144,169],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100641537","experimental-pbt-study-in-fall-prone-subjects-100641537",false,"NCT07654335","Experimental PBT Study in Fall-prone Subjects","Experimental Perturbation-based-training Study in Patients After Stroke and Older Adults","PACE-R","Inclusion Criteria for both arms:\n\n* ability for independent community walking without aids;\n* sufficient cognitive, visual, and communication abilities for study participation.\n\nExclusion Criteria for both arms:\n\n* musculoskeletal impairments;\n* cardiovascular health-related problems;\n* other health conditions that could interfere with the training.\n\nAdditional Inclusion Criteria for post-stroke patients:\n\n* discharge from their regular rehabilitation;\n* at least 6 months after first unilateral cerebral stroke;\n* 18 to 70 years of age;\n* absence of additional neurologic conditions.\n\nAdditional Inclusion Criteria for older adults:\n\n* age 65 to 75 years;\n* no known health-related problems significantly affecting balance and walking.","ALL","18 Years","75 Years",{"count":21,"type":22},50,"ESTIMATED","INTERVENTIONAL",[25],"NA","The study will investigate safety, usability, feasibility and preliminary efficacy of perturbation-based training in participants post-stroke and older adults with mild balance deficits. Both group will receive three weks of training. The primary outcome measure will be derived from laboratory-induced falls.",[28,29],"Stroke","Aging",[31,32,33,34],"Accidental Falls","Walking","Fall prevention","Perturbation-based training","NOT_YET_RECRUITING","2026-06-19",{"date":38,"type":39},"2026-06-24","ACTUAL",{"date":41,"type":22},"2026-09",{"date":43,"type":22},"2028-09",{"name":45,"class":46},"University Rehabilitation Institute, Republic of Slovenia","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":58,"briefSummary":59,"conditions":60,"keywords":61,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":47},"100565373","perceptions-of-rehatt-mixed-reality-system-100565373","NCT06641336","Perceptions of RehAtt Mixed Reality System","Perceptions of Using RehAtt Mixed Reality System in Stroke Motor Rehabilitation","RehAtt","Inclusion Criteria:\n\n* first ischaemic or hemorrhagic stroke,\n* one-sided hemiparesis,\n* adequate cognitive abilities.\n\nExclusion Criteria:\n\n* severe cognitive impairment,\n* aphasia,\n* known presence of an epileptic seizure in the last year,\n* other orthopaedic and neurological diseases affecting sensory or motor functions,\n* inability to sit independently,\n* severe visual impairment,\n* severe depression.",{"count":57,"type":22},10,[25],"The study aims to explore the patients' perspective on usability and feasibility of the RehAtt™ mixed-reality system during upper limb, gait and balance function rehabilitation.",[28],[62,63,64,65],"rehabilitation","mixed reality","motor rehabilitation","patients' perspective","RECRUITING","2026-06-11",{"date":69,"type":39},"2026-06-15",{"date":71,"type":39},"2024-10-11",{"date":73,"type":22},"2026-10",{"name":45,"class":46},{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":86,"conditions":87,"keywords":90,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":96,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":100,"locationsCount":47},"100565659","usability-of-the-smart-hallway-system-in-clinical-setting-100565659","NCT06645054","Usability of the Smart Hallway System in Clinical Setting","Smart Hallway for Gait Assessment","SmartHallway","Inclusion Criteria:\n\n* ability to walk at least 10 metres without help of a person,\n* no severe cognitive problems (able to answer questionnaires),\n* native Slovenian speakers,\n* wiling to participate (signed informed consent)\n\nExclusion Criteria:\n\n* severe cognitive impairment,\n* not being able to walk with or without a prosthesis or orthosis.",{"count":84,"type":22},100,"OBSERVATIONAL","The aim of the study is to examine suitability of data and processed reports acquired from the Smart Hallway system for clinical settings in terms of user acceptability and accuracy for use in clinical practice.",[88,89],"Amputation","Gait Disorders, Neurologic",[91,92,93,94,95],"Gait analysis","Computerised assessment","Rehabilitation","Lower limb loss","Prosthetics and orthotics",{"date":69,"type":39},{"date":98,"type":39},"2024-03-24",{"date":41,"type":22},{"name":45,"class":46},{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":107,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":109,"targetDuration":4,"studyType":23,"phases":111,"briefSummary":112,"conditions":113,"keywords":115,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":119,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"locationsCount":47},"100522999","effectiveness-of-robot-assisted-upper-limb-exercise-in-cervical-sci-100522999","NCT06089915","Effectiveness of Robot-assisted Upper-limb Exercise in Cervical SCI","Assessing Effectiveness of Robot-assisted Upper-limb Exercise in Persons After Cervical Spinal Cord Injury","RVZU","Inclusion Criteria:\n\n* ability to move unloaded upper limbs\n* at least 18 years of age\n* ability to sit for one hour\n* ability to understand the instructions for robot-assisted exercise\n\nExclusion Criteria:\n\n* inability to sit for one hour\n* presence of hospital-acquired infection that requires isolation\n* bodily impairment other than spinal cord injury\n* inability to understand the instructions for robot-assisted exercise",{"count":110,"type":22},30,[25],"The aim of the project is to test the effectiveness of robot-assisted upper-limb exercise in persons after cervical spinal cord injury. In a randomised controlled two-arm trial, the effect of adding two types of robot-assisted upper-limb exercise to standard occupational therapy will be tested. Three primary and two secondary outcomes will be assessed using well-established measures.",[114],"Cervical Vertebrae Injury",[116,117,118,62],"spinal cord injury","upper limbs","impairment",{"date":69,"type":39},{"date":121,"type":39},"2023-09-01",{"date":123,"type":22},"2026-12",{"name":45,"class":46},{"id":126,"slug":127,"hasResults":11,"nctId":128,"briefTitle":129,"officialTitle":130,"acronym":131,"eligibilityCriteria":132,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":133,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":135,"conditions":136,"keywords":4,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":138,"startDateStruct":139,"completionDateStruct":141,"leadSponsor":143,"locationsCount":47},"100465135","dysphagia-qol-and-attitudes-towards-peg-in-als-patients-100465135","NCT05336760","Dysphagia, QoL and Attitudes Towards PEG in ALS Patients","Dysphagia, Quality of Life and Attitudes Towards Percutaneous Endoscopic Gastrostomy in Patients With Amyotrophic Lateral Sclerosis","ALSDPEG","Inclusion Criteria for patients:\n\n* 18 years of age or older\n* diagnosis of ALS\n* follow-up at University Medical Centre Ljubljana, Division of Neurophysiology, every 3 months\n* be able to visit the study site for in-person procedures every 3 months\n\nInclusion Criteria for relatives:\n\n* at least 18 years of age\n\nExclusion Criteria for patients:\n\n* co-existing illness or disorder that could influence the swallowing function independently of the ALS diagnosis\n* clinically significant cognitive deterioration or dementia at enrollment, as determined by the ALS study neurologist\n\nExclusion criteria for relatives:\n\n* signs of probable cognitive deterioration or dementia at enrollment",{"count":134,"type":22},60,"In Amyotrophic Lateral Sclerosis, dysphagia has a high incidence. With deterioration of swallowing function, percutaneous endoscopic gastrostomy (PEG) tube is recommended to ensure sufficient and safe oral intake. Dysphagia and PEG placement alter quality of life (QoL). However, QoL and attitudes toward PEG remain largely unexplored. The purpose of this study is to monitor the swallowing function in relationship to QoL and attitudes toward PEG tube insertion and feeding.",[137],"Amyotrophic Lateral Sclerosis",{"date":69,"type":39},{"date":140,"type":39},"2023-01-01",{"date":142,"type":22},"2026-09-30",{"name":45,"class":46},{"id":145,"slug":146,"hasResults":11,"nctId":147,"briefTitle":148,"officialTitle":149,"acronym":150,"eligibilityCriteria":151,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":152,"targetDuration":4,"studyType":23,"phases":154,"briefSummary":155,"conditions":156,"keywords":159,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":164,"startDateStruct":165,"completionDateStruct":167,"leadSponsor":168,"locationsCount":47},"100437390","goal-attainment-scaling-in-upper-limb-spasticity-treatment-100437390","NCT04975646","Goal Attainment Scaling in Upper Limb Spasticity Treatment","Goal Attainment Scaling in Upper Limb Spasticity Treatment With Botulinum Toxin and the Influence of Regular Exercise for Spastic Upper Limb on Quality of Life in Patients After Stroke","GASBTX","Inclusion Criteria:\n\n* patient's or caregiver's approval\n* ischemic or hemorrhagic stroke diagnosed using head CT\u002FMRI\n* at least one upper limb muscle spasticity (MAS ≥ 3)\n* candidate for BTX-A treatment or already given BTX-A in the past\n* patient's or caregiver's capability for goal attainment protocol cooperation (Mini Mental Examination ≥ 24 points)\n\nExclusion Criteria:\n\n* aphasic patients without caregiver's presence\n* other neurological or musculoskeletal diseases that could affect the treatment outcome",{"count":153,"type":22},70,[25],"Patients after stroke with upper limb spasticity treated with botulinum toxin-A (BTX-A) will be included in this two-part study. In the first part, goal attainment scaling and comprehensive assessment of motor functioning will be performed before BTX-A application and after two weeks. In the second part, the patients will be randomised into a test group performing prescribed regular exercise for two weeks and a control group exercising at their own discretion during the same period, whereby the patients' health-related quality of life will be assessed at the beginning and end of the two-week period.",[157,158],"Ischemic Stroke","Hemorrhagic Stroke",[62,160,161,162,163],"spasticity","botulinum toxin A","goal setting","spasticity-related quality of life",{"date":69,"type":39},{"date":166,"type":39},"2021-01-03",{"date":73,"type":22},{"name":45,"class":46},{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":175,"eligibilityCriteria":176,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":177,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":179,"conditions":180,"keywords":184,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":189,"startDateStruct":190,"completionDateStruct":192,"leadSponsor":193,"locationsCount":47},"100368519","urinary-disorders-in-subacute-patients-after-stroke-100368519","NCT04078373","Urinary Disorders in Subacute Patients After Stroke","Assessment and Treatment of Urinary Disorders in Patients in the Subacute Phase After Stroke","UIMK","Inclusion Criteria:\n\n* subacute patients after ischaemic or hemorrhagic stroke;\n* direct transfer from acute hospital to complex inpatient rehabilitation at our Institute.\n\nExclusion Criteria:\n\n* incontinence before stroke;\n* previous brain injury or other brain disease;\n* previous bladder or prostate surgery;\n* inability to ambulate before stroke;\n* terminal disease with expected survival less than three months.",{"count":178,"type":22},250,"This observational study will address urinary disorders in subacute stroke patients. Patients without and with urinary disorders will be compared, and treatment outcome will be assessed among the latter.",[181,182,183],"Stroke, Ischemic","Stroke Hemorrhagic","Urinary Incontinence",[185,186,187,188],"stroke","inpatient rehabilitation","urinary disorders","treatment",{"date":69,"type":39},{"date":191,"type":39},"2019-06-01",{"date":73,"type":22},{"name":45,"class":46},""]