[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sensorimotor-impairment-affecting-the-upper-limb\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sensorimotor-impairment-affecting-the-upper-limb":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,59],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":46,"whyStopped":4,"lastUpdateSubmitDate":47,"lastUpdatePostDateStruct":48,"startDateStruct":51,"completionDateStruct":53,"leadSponsor":55,"locationsCount":58},"100590052","effectiveness-of-active-exploration-of-simulated-textures-for-sensorimotor-recovery-100590052",false,"NCT06962397","Effectiveness of Active Exploration of Simulated Textures for Sensorimotor Recovery","Research on the Effectiveness of the Method of Active Examination of Artificially Simulated Textures Generated by Programmable Transcutaneous Electrical Stimulation as a Method of Restoring Sensorimotor Function of the Upper Limbs","Inclusion Criteria:\n\n* Episode of stroke confirmed by neuroimaging\n* More than one month post-stroke\n* Montreal Cognitive Assessment (MoCA) score ≥ 20\n* Barthel Index score ≥ 3\n* Ability to understand and follow instructions\n* Informed consent for participation and data collection\n* Age 18-80 years\n\nExclusion Criteria:\n\n* Presence of depressive symptoms (HADS-Depression \\> 11)\n* Upper limb paresis score below 35 on the Fugl-Meyer scale\n* Sensory impairment score below 3 or above 10 on the Fugl-Meyer scale","ALL","18 Years","80 Years",{"count":20,"type":21},20,"ESTIMATED","INTERVENTIONAL",[24],"NA","Parallel-group, single-blinded controlled clinical trial. The study includes people aged 18-80 years, more than one month after stroke, with confirmed diagnosis, MoCA ≥ 20, and Barthel Index ≥ 3.\n\nThe control group receives standard rehabilitation. The experimental group also receives active sensory training with programmable electrical stimulation to simulate virtual textures.\n\nSensory function was assessed before and after the training using standard tests, including Fugl-Meyer, ARAT, 9HPT, and monofilament testing.",[27,28,29,30,31],"Stroke","Sensorimotor Impairment Affecting the Upper Limb","Sensory Deficit","Rehabilitation","Tactile Disorders",[27,33,34,35,36,37,38,39,40,41,42,43,44,45],"Sensorimotor rehabilitation","Tactile stimulation","Upper limb recovery","Electrical stimulation","Virtual textures","Sensory training","Neurorehabilitation","Post-stroke therapy","Active touch paradigm","Functional electrical stimulation","Proprioception","Touch sensitivity","Stroke rehabilitation technology","RECRUITING","2025-05-19",{"date":49,"type":50},"2025-05-22","ACTUAL",{"date":52,"type":50},"2024-10-08",{"date":54,"type":21},"2026-01",{"name":56,"class":57},"Federal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health","OTHER",1,{"id":60,"slug":61,"hasResults":11,"nctId":62,"briefTitle":63,"officialTitle":63,"acronym":64,"eligibilityCriteria":65,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":66,"targetDuration":4,"studyType":22,"phases":68,"briefSummary":69,"conditions":70,"keywords":4,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":58},"100584746","reliability-of-sensor-derived-measurements-of-the-sensorized-fugl-meyer-fma-in-subjects-with-stroke-outcomes-100584746","NCT06893367","Reliability of Sensor-Derived Measurements of the SENSorized Fugl-Meyer (FMA) in Subjects with Stroke Outcomes","FMA-SENS","Inclusion Criteria:\n\n* age 18 years or older;\n* stroke outcomes with the presence of sensorimotor impairment in the upper limb;\n* willingness to participate in the project, with informed consent signed by the person himself or, when necessary, by the support administrator\u002Flegal guardian.\n\nExclusion Criteria:\n\n* Severe concomitant pathologies that modify the subject's motor framework;\n* severe visual and\u002For hearing impairments that cannot be corrected;\n* severe neuropsychological impairments (aphasia, apraxia, other cognitive deficits ) such as to prevent cooperation in administering the scale;\n* presence of signs of clinical instability, defined by a score greater than zero on the SIC scale (Clinical Instability Scale).",{"count":67,"type":21},50,[24],"This study will be conducted at a single research center, the main objective of the study will be to evaluate the efficacy, safety, and accuracy of a medical device that has not yet been commercialized; therefore, it is still under development or testing and is not yet available for private use and is not for profit (nonprofit).\n\nFifty participants will be recruited from subjects afferent to the outpatient and inpatient neuro-motor rehabilitation clinics of IRCCS Fondazione Don Carlo Gnocchi in Florence, Italy, and afferent to the outpatient and inpatient rehabilitation clinics of Elias University Emergency Hospital in Bucharest, Romania.\n\nIn detail, it is deemed necessary to collect clinical and instrumental data. The study will be conducted by an interdisciplinary team composed of healthcare professionals and engineers afferent to the Department of Industrial Engineering.\n\nShould you decide to participate in the study, a visit to verify the inclusion and exclusion criteria will be primarily conducted. Once the admission criteria have been verified, participants will undergo a series of assessments.\n\nThe first, involves the administration of some specific sections of the Fugl-Meyer scale (FMA), focusing on the upper extremities. Specifically, the following will be examined: section A for general upper limb function, section B assessing wrist mobility, and finally section D for limb coordination and speed.\n\nDuring this phase, both upper limbs will be assessed, in addition, the first examiner will carefully place sensors on the participants and assign scores to the tests performed, according to the criteria established by the FMA scale.\n\nNext, a second assessment (T1) will be conducted, in which a second examiner will be responsible for placing the sensors and recording data only on the most affected side.\n\nAt a third time, called \"T2\" and again with at least 15 minutes interval from T1, the first examiner will repeat the same assessments performed in \"T1.\" While performing these assessments, a RealSense camera will be used.",[27,28,71],"18 Years and Over","NOT_YET_RECRUITING","2025-03-18",{"date":75,"type":50},"2025-03-25",{"date":77,"type":21},"2025-05",{"date":79,"type":21},"2026-05",{"name":81,"class":57},"Fondazione Don Carlo Gnocchi Onlus"]