[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-anterior-instability\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-anterior-instability":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"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":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":46,"locationsCount":5},"100603175","evaluating-upper-limb-movement-precision-with-aureha-in-people-with-one-sided-motor-impairment-100603175",false,"NCT07133100","Evaluating Upper Limb Movement Precision With AuReha in People With One-Sided Motor Impairment","Intrasubject Evaluation of Upper Limb Movement Precision Using the AuReha System in Individuals With Unilateral Motor Impairment","Inclusion Criteria:\n\n* patients with a healthy contralateral limb\n* patients affected by orthopedic shoulder conditions such as posterior instability, anterior instability, anterior Latarjet instability, adhesive capsulitis, or prostheses\n* age ≥18 years\n* patients who consent to participate in the study by signing the informed consent form\n\nExclusion Criteria:\n\n* Pregnant and\u002For breastfeeding women (verified through self-declaration)\n* Epilepsy\n* Allergy or hypersensitivity to materials used in the medical device, specifically: polypropylene and lycra (fabric), nylon (integrated zipper), viscose and elastane (zipper integration fabric)\n* Chronic headache under treatment","ALL","18 Years",{"count":19,"type":20},52,"ESTIMATED","INTERVENTIONAL",[23],"NA","The clinical investigation is designed as a controlled, two-arm, intra-patient, non-randomized interventional study aimed at assessing the capabilities of the AuReha system in detecting upper limb movement precision in patients with unilateral proprioceptive impairment. The comparison will be conducted within the same subject, between the healthy limb and the impaired limb, through the execution of proprioceptive exercises in an open kinetic chain. The biomechanical parameters collected will include movement precision, trunk stability, compensatory movements, and joint range of motion. In addition to the quantitative analysis, qualitative data will also be collected regarding usability, wearability, and user experience of the system through questionnaires administered to both patients and healthcare professionals.\n\nThe study will be conducted at the Shoulder Team Outpatient Clinic in Forlì, enrolling approximately 52 patients.",[26,27,28,29,30],"Shoulder Posterior Instability","Shoulder Anterior Instability","Shoulder Anterior Latarjet Instability","Adhesive Capsulitis, Shoulder","Prostheses",[32,33,34,35,36,37],"wearable medical device","upper limb rehabilitation","inertial measurement sensors","monitoring system","supporting system","shoulder rehabilitation","NOT_YET_RECRUITING","2025-09-30",{"date":41,"type":42},"2025-10-01","ACTUAL",{"date":44,"type":20},"2025-10",{"date":44,"type":20},{"name":47,"class":48},"DigitalRehab","INDUSTRY"]