[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100650989":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":26,"locations":35,"responsibleParty":53,"collaborators":20,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":20,"eligibilityCriteria":62,"healthyVolunteers":58,"sex":63,"minAge":64,"maxAge":65,"enrollmentInfo":66,"targetDuration":20,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":77,"overallStatus":79,"whyStopped":20,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"MultiCare Health System Research Institute","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Impact of Motus Nova Foot on Gait and Balance for Individuals with Hemiplegia","EXPERIMENTAL","Participants will complete a home-based intervention using the Motus Nova Foot device for approximately 8-10 weeks. The device provides robot-assisted ankle\u002Ffoot movement and interactive computer-guided therapeutic activities designed to improve ankle range of motion, strength, motor control, and gait mechanics. Participants are instructed to use the device 20-40 minutes per day, 4-5 days per week. Activities include 3-5 guided tasks targeting dorsiflexion, plantarflexion, and functional ankle control, with the device automatically recording usage and duration. Families receive an initial in-lab device fitting and training session, and research staff provide weekly check-ins (virtual or in-person) for troubleshooting and adherence support. After the intervention phase, participants complete an 8-10-week no-treatment carryover period with no device use to assess retention of gains.",[13],"Device: Motus Nova Foot",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","Motus Nova Foot","Motus Nova Foot device used in home therapy to improve gait for individuals with hemiplegia.",[9],null,[22],{"name":23,"affiliation":24,"role":25},"Brenna Brandsma, PT, DPT, PCS","MultiCare, Mary Bridge Children's Therapy Research & Movement Lab","PRINCIPAL_INVESTIGATOR",[27,31],{"name":23,"role":28,"phone":29,"phoneExt":20,"email":30},"CONTACT","12536975268","babrandsma@multicare.org",{"name":32,"role":28,"phone":33,"phoneExt":20,"email":34},"Sean Brown, PhD","253-697-5402","sean.brown@multicare.org",[36],{"facility":37,"status":20,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Mary Bridge Children's Therapy Research & Movement Lab","Puyallup","Washington","98372","United States","US",{"type":44,"coordinates":45},"Point",[46,47],-122.2929,47.18538,{"lat":47,"lon":46},[50,52],{"name":23,"role":28,"phone":51,"phoneExt":20,"email":30},"253-697-5268",{"name":32,"role":28,"phone":33,"phoneExt":20,"email":34},{"type":25,"investigatorFullName":54,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"Brenna Brandsma","Physical Therapist","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":67,"type":68},5,"ESTIMATED","INTERVENTIONAL",[71],"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.",[74,75,76],"Hemiplegia","Cerebral Palsy","Hemiplegic Cerebral Palsy",[17,78,75,74],"Gait Analysis","NOT_YET_RECRUITING","2026-08-04",{"date":82,"type":83},"2026-08-10","ACTUAL",{"date":85,"type":68},"2026-09",{"date":87,"type":68},"2027-12",{"name":5,"class":6},1]