[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Loewenstein Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":131},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,41,60,82,102],{"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":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100569162","self-practicing-upper-body-exercises-with-a-robotic-trainer-system-100569162",false,"NCT06690658","Self-Practicing Upper Body Exercises With a Robotic Trainer System","Self-Practicing Upper Body Exercises With a Robotic Trainer System in the Physical Therapy Department: A Feasibility Study","Inclusion Criteria:\n\n* 18 years ≤ Age\n* stable clinical and metabolic state\n* ability to sit without back support independently\n* ability to understand research instructions.\n\nExclusion Criteria:\n\n* A contraindication to perform active upper extremity movements\n* Severe pain that limits the ability to exercise.","ALL","18 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","Studies suggest that older adults undergoing inpatient rehabilitation have relatively low levels of physical activity. Moreover, people with lower limb orthopedic conditions undergoing inpatient rehabilitation may be particularly vulnerable to the consequences of low physical activity because of the mobility limitations.\n\nThe study focuses on examining the feasibility of incorporating robotic system for upper body physical training of people with lower limb orthopedic condition undergoing inpatient rehabilitation. Using robotic coaches can be a complementary method to promote the participation and motivation of people with lower limb orthopedic conditions undergoing inpatient rehabilitation.\n\nAims:\n\nThe overall aim of the study is to assess the user experience and feasibility of incorporating robotic system for upper body physical training of people with lower limb orthopedic injury\u002Fcondition undergoing inpatient rehabilitation. Our specific aims are:\n\n1. To assess the acceptability and suitability of the training (i.e., training attendance and engagement; adherence to training protocol; time on task; satisfaction and enjoyment of the training)\n2. To document unexpected adverse events during training.\n3. To assess the resources and ability to manage and implement the training (i.e., administrative capacity, technology and equipment needs and training).",[26,27],"Robot Assisted Therapy","Training","RECRUITING","2026-05-25",{"date":31,"type":32},"2026-05-27","ACTUAL",{"date":34,"type":32},"2025-01-21",{"date":36,"type":20},"2027-01",{"name":38,"class":39},"Loewenstein Hospital","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":47,"targetDuration":4,"studyType":21,"phases":48,"briefSummary":49,"conditions":50,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":52,"lastUpdatePostDateStruct":53,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":40},"100476291","speaking-valve-influence-on-breathing-swallowing-and-vocal-functions-in-patients-with-tracheostomy-100476291","NCT05482022","Speaking Valve Influence on Breathing, Swallowing and Vocal Functions in Patients With Tracheostomy.","Inclusion Criteria:\n\n* brain injury (traumatic\u002Fnon-traumatic).\n* tracheostomy.\n* unresponsive wakefulness syndrome or minimally conscious state.\n* fiber optic examination as follows: good mobilization of the vocal cords. No airway granulation, MarianJoy scale score: 1-3.\n* the legal guardian speaks Hebrew.\n\nExclusion Criteria:\n\n* airway stenosis \u002F inflammation.\n* oxygen saturation \\\u003C90%.",{"count":19,"type":20},[23],"Speaking valve seems to have a beneficial influence on breathing and secretion management in certain patients with tracheostomy.\n\nThe investigators plan to use a speaking valve during respiratory physical therapy sessions in participants with disturbances of consciousness, who have a tracheostomy, with no need of a mechanical ventilation.",[51],"Tracheostomy","2025-08-10",{"date":54,"type":32},"2025-08-14",{"date":56,"type":32},"2022-08-01",{"date":58,"type":20},"2026-01-15",{"name":38,"class":39},{"id":61,"slug":62,"hasResults":11,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":4,"eligibilityCriteria":66,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":67,"targetDuration":4,"studyType":21,"phases":69,"briefSummary":70,"conditions":71,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":40},"100521232","prophylactic-pregabalin-treatment-following-spinal-cord-injury-100521232","NCT06066918","Prophylactic Pregabalin Treatment Following Spinal Cord Injury","The Effect of Preventional Drug Therapy on Pain Regulation Mechanisms Among Spinal Cord Injury Patients Who Have Yet to Develop Central Pain","Inclusion Criteria:\n\n* Up to 3 months following traumatic or non-traumatic SCL\n* Ability to give informed consent and cooperate\n\nExclusion Criteria:\n\n* Pregnancy\n* Neurological or other medical conditions that may interfere with sensation\n* Neuropathic-like pain before recruitment (described as painful sensation of electric current, burning, numbness, tingling, pricking, or squeezing)\n* Being treated with Pregabalin\n* Blood creatinine levels \\>1.2 or creatinine clearance \\\u003C60\n* Sensitivity to lactose",{"count":68,"type":20},50,[23],"Patients arriving to rehabilitation up to 3 months following SCI will be given (study group) or not (control group) Lyrica (75X2). They will be followed for central pain development.",[72,73],"Spinal Cord Injuries","Spinal Cord Diseases","2025-06-18",{"date":76,"type":32},"2025-06-24",{"date":78,"type":32},"2021-07-13",{"date":80,"type":20},"2026-02-05",{"name":38,"class":39},{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":21,"phases":90,"briefSummary":91,"conditions":92,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":40},"100476486","prevention-of-thromboembolism-using-apixaban-vs-enoxaparin-following-spinal-cord-injury-100476486","NCT05484557","Prevention of Thromboembolism Using Apixaban vs Enoxaparin Following Spinal Cord Injury","Inclusion Criteria:\n\n* spinal cord injury (traumatic of not traumatic), Hebrew speaker.\n\nExclusion Criteria:\n\n* contra-indication for anticoagulant treatment\n* concomitant treatment with any other anticoagulant\n* anticoagulant treatment needed for indications other than VTE prevention following spinal cord injury\n* active clinically significant bleeding\n* any lesion or condition considered a significant risk factor for major bleeding.\n* hepatic disease associated with coagulopathy and clinically relevant bleeding risk\n* pregnancy or breast-feeding\n* heart valve related issues\n* galactose intolerance\n* active cancer\n* patients who require thrombolysis or pulmonary embolectomy\n* patients with renal impairment\n* sensitivity to excipients of the medication\n* anti phospholipid syndrome\n* prosthetic heart valve\n* acute ischemic stroke",{"count":89,"type":20},60,[23],"Currently, Enoxaparin is the usual prophylactic anticoagulant treatment at the acute and sub-acute phases of spinal cord injury (SCI). Patients at the sub-acute phase of SCI (rehabilitation) will be given either Enoxaparin 40 mg\u002Fday (control) or Apixaban 2.5-5 mg twice a day. Apixaban dose will be determined by the treating physician. Treatment will be continued for either 6 or 12 weeks following injury (for AIS grades C-D and A-B respectively).\n\nEndpoints: Venous thromboembolism will be evaluated by D-Dimer test every 2 weeks and an ultrasound doppler at the beginning and the end of the treatment. Bleeding events will be recorded and hematocrit will be monitored every two weeks.",[72,93],"Spinal Diseases","2025-05-06",{"date":96,"type":32},"2025-05-09",{"date":98,"type":32},"2023-09-06",{"date":100,"type":20},"2026-02",{"name":38,"class":39},{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":109,"sex":16,"minAge":17,"maxAge":110,"enrollmentInfo":111,"targetDuration":4,"studyType":21,"phases":113,"briefSummary":114,"conditions":115,"keywords":118,"overallStatus":122,"whyStopped":4,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":4},"100570504","examining-the-feasibility-of-an-outdoor-therapeutic-horse-carriage-as-a-perturbation--based-balance-training-100570504","NCT06708104","Examining the Feasibility of an Outdoor Therapeutic Horse Carriage As a Perturbation -based Balance Training","Examining the Feasibility of an Outdoor Therapeutic Horse Carriage As a Perturbation -based Balance Training.","Inclusion Criteria:\n\n* Healthy young participants\n* Adults aged 18-45 years\n* Measuring between150-190 cm in stature, with a mass of less than 100 kg\n* No neurological or vestibular or orthopedic mobility impairing conditions, and with no current musculoskeletal injury.\n\nExclusion Criteria:\n\n* blindness or serious vestibular impairments (Meniere's disease, dizziness)\n* an inability to ambulate independently\n* symptomatic severe cardiovascular disease\n* neurological disorders such as stroke, Parkinson's, or Multiple sclerosis\n* orthopedic acute disorders requiring total hip or knee replacement\n* severe rheumatoid arthritis; and\u002For (g) cancer (metastatic or under active treatment).",true,"45 Years",{"count":112,"type":20},15,[23],"The proposed study is a prospective experimental single-arm pre-post study aiming to assess the effectiveness and feasibility of an outdoor therapeutic horse carriage, i.e., the Equine Dynamic Balance (EDB), as a form of reactive balance training. First, the investigators will describe the mechanical parameters of perturbations generated by the EDB's standing platform, including displacement, velocity and acceleration. Second, the investigators will assess the effect of EDB training on balance. Independent healthy young adults who do not suffer from balance impairments willing to participate in the study will be tested before and after EDB training, that will be delivered by standing on a dynamic therapeutic horse carriage pulled by a horse, to explore whether there are differences in balance control and balance reactions as a result of a 2-week EDB intervention program.",[116,117],"Balance Impairment","Accidental Fall",[119,120,121],"Reactive balance","Perturbation training","Animal-assisted therapy","NOT_YET_RECRUITING","2024-11-24",{"date":125,"type":32},"2024-11-27",{"date":127,"type":20},"2024-12",{"date":129,"type":20},"2025-08",{"name":38,"class":39},""]