[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"MultiCare Health System Research Institute\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":76},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"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":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100650989","motus-nova-foot-device-for-patients-with-hemiplegia-100650989",false,"NCT07754773","Motus Nova Foot Device for Patients With Hemiplegia","Evaluating Gait After Use of The Motus Nova Foot Device for Patients With Hemiplegia","Inclusion Criteria:\n\n* Age 12-20 years.\n* Diagnosis consistent with hemiplegia and gait\u002Fbalance impairments involving ankle\u002Ffoot control (e.g., reduced heel strike).\n* Able to ambulate and safely participate in laboratory walking and balance testing.\n* Able to follow instructions and use the Motus Nova Foot system at home with family support as needed.\n* Willingness to refrain from standard clinic-based PT during the study period.\n\nExclusion Criteria:\n\n* Skin integrity issues or hypersensitivity preventing safe use of straps\u002Fpads.\n* Medical\u002Forthopedic conditions making walking or balance testing unsafe (e.g., unstable seizures, recent surgery, acute injury).\n* Inability to safely use the device as determined during fitting\u002Ftraining.\n* Planned participation in standard clinic-based PT during the study period.\n* Electrical stimulation device to lower extremity within 6 months of study start, or planned use of electrical stimulation to lower extremity during study period.\n* Heart conditions that prevent physical activity.\n* Pregnancy.","ALL","12 Years","20 Years",{"count":20,"type":21},5,"ESTIMATED","INTERVENTIONAL",[24],"NA","Individuals with hemiplegia commonly demonstrate gait deviations such as difficulties with heel strike at initial contact, foot drop in swing, asymmetrical limb loading, muscle activation, and balance impairments. This study evaluates whether a therapeutic device (Motus Nova Foot; FDA approved) used in the home setting can increase heel strike, decrease limp, improve foot clearance in swing phase, improve quality of active muscle contraction of the affected limb, and improve balance. The Motus Nova Foot moves the ankle\u002Ffoot and uses guided computer\u002Fvideo activities to encourage active participation while automatically recording device use and duration.",[27,28,29],"Hemiplegia","Cerebral Palsy","Hemiplegic Cerebral Palsy",[31,32,28,27],"Motus Nova Foot","Gait Analysis","NOT_YET_RECRUITING","2026-08-04",{"date":36,"type":37},"2026-08-10","ACTUAL",{"date":39,"type":21},"2026-09",{"date":41,"type":21},"2027-12",{"name":43,"class":44},"MultiCare Health System Research Institute","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":16,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":45},"100535288","pediatric-normative-markerless-movement-analysis-100535288","NCT06249880","Pediatric Normative Markerless Movement Analysis","Pediatric Normative Markerless Movement Analysis Data Collection Project","Inclusion Criteria:\n\n* Age: 3-25 years of age (with 3 and 25 year olds considered for inclusion).\n* Ambulate independently and without the use of assistive devices or orthoses.\n* Willing and interested in participating.\n\nExclusion Criteria:\n\n* Neuromuscular disorders such as cerebral palsy, muscular dystrophy, myotonic dystrophy, spinal muscular atrophy, peripheral neuropathy, or other generalized muscle and\u002For nerve issues.\n* Evidence of developmental delays, muscle weakness, decreased muscle tone, joint stiffness, muscle or bone deformity.\n* Currently using or has a history of using assistive technology devices, bracing\u002Forthoses, manual or powered mobility equipment.\n* History of premature birth.\n* Currently or has a history of taking medication or pharmaceutical treatment related to musculoskeletal side-effects\u002Fscenario\u002Fdiagnosis.",true,"3 Years","25 Years",{"count":57,"type":21},40,"OBSERVATIONAL","The objective of this project is to collect baseline data from a normative population of 20 children that gender and age matches the population of patients expected to be treated by Mary Bridge Children's Research \\& Movement Lab.",[61,62],"Pediatric ALL","Adolescent",[64,65,66],"Motion Analysis","Kinetics","Kinematics","RECRUITING","2026-03-05",{"date":70,"type":37},"2026-03-09",{"date":72,"type":37},"2024-03-01",{"date":74,"type":21},"2028-12",{"name":43,"class":44},""]