[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100530912":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":24,"locations":34,"responsibleParty":53,"collaborators":18,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":57,"sex":62,"minAge":63,"maxAge":64,"enrollmentInfo":65,"targetDuration":18,"studyType":68,"phases":69,"briefSummary":71,"conditions":72,"keywords":18,"overallStatus":37,"whyStopped":18,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":83},{"fullName":5,"class":6},"Centre Hospitalier Universitaire de Nice","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Stimulated group","EXPERIMENTAL","5 sessions per week for 6 weeks maximum of reeducation with Functional Proprioceptive Stimulation",[13],"Other: Functional Proprioceptive Stimulation",{"label":15,"type":16,"description":17,"interventionNames":18},"Simulated group","NO_INTERVENTION","5 sessions per week for 6 weeks maximum with the device of Functional Proprioceptive Stimulation settled but not activated",null,[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":18},"Functional Proprioceptive Stimulation","Orthoses with a system of 12 stimulators producing mechanical oscillations are attached to the joints of the upper limbs (wrist, elbow and shoulder) or lower limb joints (ankle, knee, hip). These stimulators, which are all synchronized, deliver mechanical oscillations (FPS) that give the illusion of complex movements, while the patient is bedridden, neither moving nor producing effort.",[9],[25,30],{"name":26,"role":27,"phone":28,"phoneExt":18,"email":29},"Guillaume SACCO, MD","CONTACT","04 92 03 47 51","sacco.g@chu-nice.fr",{"name":31,"role":27,"phone":32,"phoneExt":18,"email":33},"Justine LEMAIRE","+33492034778","lemaire.j@chu-nice.fr",[35],{"facility":36,"status":37,"city":38,"state":18,"zip":18,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"CHU de Nice","RECRUITING","Nice","France","FR",{"type":42,"coordinates":43},"Point",[44,45],7.26608,43.70313,{"lat":45,"lon":44},[48,50],{"name":49,"role":27,"phone":18,"phoneExt":18,"email":18},"Justine Lemaire",{"name":51,"role":52,"phone":18,"phoneExt":18,"email":18},"Guillaume SACCO","PRINCIPAL_INVESTIGATOR",{"type":54,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR","100530912","early-functional-proprioceptive-stimulation-post-stroke-100530912",false,"NCT06192953","Early Functional Proprioceptive Stimulation Post-stroke","StimProF","Inclusion Criteria:\n\n* Adult patient hospitalized at Cimiez University Hospital;\n* Ischemic or hemorrhagic cerebrovascular accident (CVA) of less than two weeks;\n* Hemiparesis requiring rehabilitation treatment;\n* Patient with a SFPASS score ≤ 6;\n* Patient affiliated to or beneficiary of a social security scheme;\n* Signature of informed consent\n\nExclusion criteria :\n\n* NIHSS \\> 20;\n* Muscle spasticity of the lower limbs requiring botulinum toxin injection\n* Inability to understand rehabilitation instructions;\n* Vulnerable people\n* Pregnant women, parturients and breastfeeding mothers, persons deprived of their liberty by a judicial or administrative decision, persons hospitalized without consent and persons admitted to a health or social establishment for purposes other than research,\n* Adults who are subject to a legal protection measure or who are unable to express their consent.","ALL","18 Years","100 Years",{"count":66,"type":67},32,"ESTIMATED","INTERVENTIONAL",[70],"NA","The main objective of our study is to evaluate the impact of the use of Functional Proprioceptive Stimulation (FPS) on the recovery of the postural and motor functional capacities of the patient in the subacute phase of a stroke.\n\nThe hypothesis is that the use of FPS has a positive impact on the recovery of the patient's functional abilities, as well as on the duration of treatment until the sit\u002Fstand transfers are completed.\n\nTo evaluate this potential effect,there will be a randomization with two groups : one will have 5 sessions a week for 6 weeks maximum of SPF and the other groupe will have the same sessions but with the device stettled but not activated.",[73],"Stroke (CVA) or TIA","2026-03-24",{"date":76,"type":77},"2026-03-27","ACTUAL",{"date":79,"type":77},"2024-05-06",{"date":81,"type":67},"2027-04-30",{"name":5,"class":6},1]