[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"upper-extremity-problem\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:upper-extremity-problem":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,70],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":21,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100462398","vivistim-registry-for-paired-vns-therapy-grasp-100462398",false,"NCT05301140","Vivistim Registry for Paired VNS Therapy (GRASP)","GRASP","Inclusion Criteria:\n\n* Patients implanted with the Vivistim System for upper limb deficits associated with an ischemic stroke\n\nExclusion Criteria:\n\n* Not eligible for surgery","ALL","22 Years",{"count":19,"type":20},1000,"ESTIMATED","3 Years","OBSERVATIONAL","The purpose of the Vivistim Registry for Paired VNS Therapy (GRASP) is to gather real-world information on patients with arm and hand deficits post-stroke who are considering Vivistim System treatment. Before and after Vivistim System implant, patient data will be collected and reported throughout the therapy process. Physicians or sites will receive appropriate remuneration for the effort and cost involved in collecting and transmitting this data to MicroTransponder Inc.",[25],"Upper Extremity Problem",[27,28],"Ischemic Stroke","Paired Vagus Nerve Stimulation","RECRUITING","2026-06-24",{"date":32,"type":33},"2026-06-29","ACTUAL",{"date":35,"type":33},"2023-03-15",{"date":37,"type":20},"2028-12-31",{"name":39,"class":40},"MicroTransponder Inc.","INDUSTRY",15,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":69},"100542943","the-utilization-effects-of-powered-wearable-orthotics-in-improving-upper-extremity-function-and-adl-in-persons-with-sci-100542943","NCT06349434","The Utilization Effects of Powered Wearable Orthotics in Improving Upper Extremity Function and ADL in Persons With SCI","Inclusion Criteria:\n\n* Be between ages 18-80\n* Be able to activate certain muscles in my arm and forearm on my own a sufficient amount as measured by EMG amplitude. This will be determined by the study OT\u002FPT.\n* Be diagnosed with spinal cord injury (SCI) with level C1-C8 and ASIA Impairment Scale (AIS) C or D, as determined by study staff. If I have not had an exam to determine my injury level and impairment scale recently, I may participate in an examination of my sensation and strength in my arms, legs, trunk and rectum as was done in the hospital soon after my injury.\n* Be at least 1-year post injury\n* Have sufficient ability to move my shoulder (active shoulder flexion of 30 degrees and active shoulder abduction 20 degrees), as determined by study staff\n* Be medically stable\n* Have sufficient learning and memory abilities and abilities to communicate in English to be able to participate and follow directions during my rehabilitation\n* Continue to take all prescribed medication (e.g., oral or via pump baclofen) without any dosing changes\n* Be able to tolerate functional tasks for 60 minutes with periodic rests without excessive fatigue\n* Have minimal strength in the muscles that bend and straighten my elbow, as determined by study staff\n* Have full range of motion in my elbow when it is moved by the study therapist\n\nExclusion Criteria:\n\n* Be younger than 18 years old or older than 80\n* Have excessive pain in my arm, wrist, or hand that limits providing rehabilitation\n* Have excessive spasticity in my elbow or wrist, as determined by study staff\n* Be participating in any experimental rehabilitation or drug studies\n* Have history of nervous system disorder other than SCI\n* Have difficulty following multiple step directions\n* Have severe cognitive or psychiatric problems might be contraindications to start training.\n* Have skin issues or severe sensory deficits that would prevent wearing the Myo-Pro device safely\n* Be pregnant\n* Have other conditions or circumstances that, in the opinion of the investigators, would affect the safety or effectiveness of the training in which I would participate","18 Years","80 Years",{"count":51,"type":20},60,"INTERVENTIONAL",[54],"NA","To evaluate the usefulness of an upper extremity assistive device, called (MyoPro) in improving upper extremity activities in people with incomplete spinal cord injury. The Department of Defense is supporting this study.",[57,58,25],"SCI - Spinal Cord Injury","Upper Extremity Dysfunction","2025-11-19",{"date":61,"type":33},"2025-11-24",{"date":63,"type":33},"2023-10-15",{"date":65,"type":20},"2028-10-01",{"name":67,"class":68},"Kessler Foundation","OTHER",1,{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":16,"minAge":76,"maxAge":77,"enrollmentInfo":78,"targetDuration":4,"studyType":52,"phases":80,"briefSummary":81,"conditions":82,"keywords":85,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":69},"100594948","effects-of-biofeedback-guided-training-on-muscle-strength-and-postural-alignment-in-upper-cross-syndrome-100594948","NCT07026084","Effects of Biofeedback-Guided Training on Muscle Strength and Postural Alignment in Upper Cross Syndrome.","Inclusion Criteria:\n\n* • Adults aged 25-45 years with both genders.\n\n  * Individuals meeting the following diagnostic criteria for upper cross syndrome will be included:\n  * Reduced strength of deep cervical flexors = unable to maintain pressure beyond 22-24 mm Hg (assessed via cranio-cervical flexion test).\n  * Limited cervical range of motion (Flexion: \\\u003C 80 degrees, Extension: \\\u003C 70 degrees, Rotation: \\\u003C 90 degrees on both sides, Lateral Flexion: \\\u003C 20 degrees)\n  * Postural deviations: forward head posture (CVA \\\u003C50 degrees), increased thoracic kyphosis (via flexi curve \\>45 degrees).\n  * Neck pain with a duration of over 3 months\n\nExclusion Criteria:\n\n* • History of recent neck surgery or injury.\n\n  * Patients with neurological disorders affecting muscle tone.\n  * Involvement in other physical therapy programs focused on UCS.\n  * Diagnosed musculoskeletal condition that could impact muscle performance.","25 Years","45 Years",{"count":79,"type":20},56,[54],"This randomized controlled trial investigates the effects of biofeedback-guided training versus conventional therapy on muscle strength and postural alignment in patients with Upper Cross Syndrome. The study includes adults aged 25-45 years meeting diagnostic criteria for UCS, such as weak deep cervical flexors, restricted cervical ROM, forward head posture, increased thoracic kyphosis, and chronic neck pain \\>3 months. Participants are divided into two groups: Group A biofeedback training and Group B conventional therapy, receiving 12 sessions over 4 weeks ,3sessions\u002Fweek. Assessments are conducted at baseline, post-1st session, and weekly intervals using standardized measures.The study aims to compare the efficacy of biofeedback-guided training in improving strength and posture in UCS patients.",[25,83,84],"Muscle Weakness","Postural Kyphosis",[86,87,88,89,90],"upper cross syndrome","forward head posture","young adults","bio feedback guided training","postural alignment","2025-08-18",{"date":93,"type":33},"2025-08-22",{"date":95,"type":33},"2025-08-11",{"date":97,"type":20},"2026-01-01",{"name":99,"class":68},"Riphah International University"]