[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"spastic-paresis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:spastic-paresis":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100628879","goat-gait-observation-of-achilles-tendon-100628879",false,"NCT07467382","GOAT (Gait Observation of Achilles Tendon)","Characterization of Mechanical Properties of Achilles Tendon During Gait in Spastic Paresis Syndrome","GOAT","Inclusion Criteria:\n\nStudy population:\n\n• Cognitive abilities compatible with the experiment: no language or judgement disorders preventing understanding of the research or expression of consent. An aphasia severity score greater than or equal to 3 on the Boston Diagnostic Aphasia Examination (BDAE) scale will be required for inclusion.\n\nPost-stroke population:\n\n* Adult male or female\n* Patient who has had a stroke \\> 7 days ago\n* Patient hospitalised (in conventional hospitalisation or day hospital) in the neurological physical and medical rehabilitation department of Nantes University Hospital\n* Patients with voluntary motor function rated between 2 and 4 on the MRC (Medical Research Council) scale at the GM level\n* Patients classified as 3 to 8 on the New Functional Ambulation Classification\n* Indication to perform a quantified gait analysis as part of clinical management\n\nPost-spinal cord injury population:\n\n* Adult men or women\n* Patients with incomplete spinal cord injury graded ASIA AIS C or D from C2 to L5\n* Patients hospitalised (in conventional hospitalisation or day hospital) in the neurological physical and occupational therapy department of Nantes University Hospital\n* Patients with voluntary motor function rated between 2 and 4 on the MRC (Medical Research Council) scale at GM level\n* Patients rated 13-20 on the WISCI-II scale\n* Indication for a quantified gait analysis as part of clinical care\n\nHealthy population:\n\n• Adult men or women with no nervous system disorders.\n\nExclusion Criteria:\n\nPost-stroke and post-spinal cord injury population:\n\n* Minors;\n* History of calf surgery, surgery to reduce triceps surae spasticity, or intramuscular injection (e.g. botulinum toxin) in the plantar flexors \\\u003C 6 months;\n* Patients with a progressive condition that contraindicates exertion (syrinx, cardiovascular instability);\n* Peripheral pathology of the lower limb in question.\n\nHealthy population:\n\n* History of calf surgery;\n* History of muscle injury, fracture or sprain of the lower limb \\\u003C 3 months;\n* History of neurological condition.",true,"ALL","18 Years",{"count":21,"type":22},60,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to evaluate the mechanical properties of the Achilles tendon (stiffness, length, volume) and the force production capacities of the gastrocnemius medialis muscle in patients with spastic paresis (post-stroke or incomplete spinal cord injury) compared to healthy subjects, during gait.",[26,27,28],"Spastic Paresis","Stroke","Spinal Cord Injury",[30,31,32,33],"Achilles tendon","Gait analysis","Ultrasound","Muscle-tendon interaction","NOT_YET_RECRUITING","2026-05-22",{"date":37,"type":38},"2026-05-27","ACTUAL",{"date":40,"type":22},"2026-06-01",{"date":42,"type":22},"2027-12-01",{"name":44,"class":45},"Nantes University Hospital","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":18,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":58,"briefSummary":60,"conditions":61,"keywords":66,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":5},"100579773","comparing-digitally-and-traditionally-made-ankle-foot-orthoses-100579773","NCT06828653","Comparing Digitally and Traditionally Made Ankle Foot Orthoses","Feasibility RCT Evaluating Digitally and Traditionally Produced Ankle Foot Orthoses for Individuals With Impaired Lower Limb Function","Inclusion Criteria:\n\n* Participants must be aged 8 years or older.\n* Participants should have either flaccid or spastic paresis resulting from conditions such as cerebral palsy, stroke, spinal cord injury, spina bifida, or traumatic peripheral nerve injury, leading to lower limb mobility impairments.\n* Participants must require a custom articulating, rigid, or energy storage and return (ESR) AFO to improve physical function for one or both sides (unilateral or bilateral).\n* Participants must be able to ambulate independently, though the use of gait aids is permitted.\n* Participants must be capable of completing questionnaires with no more than orienting guidance.\n* Participants must meet the requirements to have their AFO funded by the Assistive Devices Program (ADP).\n\nExclusion Criteria:\n\n* Clients for whom the primary goal of the AFO includes wound management.\n* Those whose AFO is not worn for ambulation.\n* Clients with insensate feet or a history of ulcerations.\n* First-time AFO users.","8 Years",{"count":56,"type":22},50,"INTERVENTIONAL",[59],"NA","The research is being done to compare two methods of creating AFOs: 1. The traditional method, which involves manually creating a mold from a plaster cast of the client's limb. This is time-consuming and labor-intensive; and 2. The newer method uses digital technology, such as 3D scanning and printing, to design and produce the AFOs, potentially making the process faster and less costly. We want to know whether AFOs made using digital technology can provide the same clinical benefits as those made traditionally.",[62,26,63,27,28,64,65],"Flaccid Paresis","Cerebral Palsy","Spina Bifida","Traumatic Peripheral Nerve Injury",[67,68,69,70,71,72,73],"Ankle foot orthosis","ankle foot orthoses","digital ankle foot orthoses","digital technology","3D scanning","3D printing","randomized control trial","RECRUITING","2025-11-18",{"date":77,"type":38},"2025-11-20",{"date":79,"type":38},"2025-09-05",{"date":81,"type":22},"2027-03-31",{"name":83,"class":45},"Holland Bloorview Kids Rehabilitation Hospital"]