[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100569288":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":34,"centralContacts":39,"locations":45,"responsibleParty":66,"collaborators":43,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":43,"eligibilityCriteria":74,"healthyVolunteers":70,"sex":75,"minAge":76,"maxAge":43,"enrollmentInfo":77,"targetDuration":43,"studyType":80,"phases":81,"briefSummary":83,"conditions":84,"keywords":86,"overallStatus":48,"whyStopped":43,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":109},{"fullName":5,"class":6},"IRCCS Eugenio Medea","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Platform Group","EXPERIMENTAL","Balance training including both conventional rehabilitation (24 sessions) and training over a stabilometric platform (20 sessions).",[13,14],"Behavioral: Balance training over stabilometric platform","Behavioral: Balance training by means of conventional rehabilitation",{"label":16,"type":17,"description":18,"interventionNames":19},"Conventional Group","ACTIVE_COMPARATOR","Balance training including only conventional rehabilitation (44 sessions).",[14],[21,28],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","Balance training over stabilometric platform","The treatment using the stabilometric platform (a total of 20 sessions) generally includes an initial phase (approximately 5 minutes) of training and warm-up in \"monitor\" mode, during which the patient becomes familiar with the equipment. The patient then moves on to \"training library\" mode, which includes the following subcategories: (1) Stabilometric tracings in both static and dynamic phases (10 minutes); (2) Dexterity exercises in both static and dynamic phases (10 minutes); (3) Imbalance exercises in both static and dynamic phases (10 minutes).\n\nThe goal during this phase is to increase the patient's stability limits and provoke balance reactions through load shifts in all directions. The session concludes with 10 minutes of TecnoBody Exergames, which help to automate the functions learned within a more complex activity.",[9],[27],"PROKIN - PK252",{"type":22,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"Balance training by means of conventional rehabilitation","Conventional rehabilitation to improve balance includes an initial phase of tissue mobilization, particularly of the foot structures (approximately 5 minutes per foot), in order to prepare them for the subsequent activation phase. This is followed by a phase focused on activating the anti-gravity muscles and aligning the trunk within the chosen setting (10 minutes). The treatment continues with balance training, both static and dynamic, load transfers, and dual-task exercises using external references (15 minutes). The session concludes with functional exercises relevant to the patient's daily life context (10 minutes).",[16,9],[33],"balance training",[35],{"name":36,"affiliation":37,"role":38},"Gabriella Paparella, Medical Degree","Scientific Institute, IRCCS E. Medea, Department of Conegliano, Treviso, Italy.","PRINCIPAL_INVESTIGATOR",[40],{"name":36,"role":41,"phone":42,"phoneExt":43,"email":44},"CONTACT","00390438906330",null,"gabriella.paparella@lanostrafamiglia.it",[46],{"facility":47,"status":48,"city":49,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":60},"Scientific Institute, IRCCS E. Medea, Department of Pieve di Soligo, Treviso, Italy","RECRUITING","Pieve di Soligo","Veneto","31053","Italy","IT",{"type":55,"coordinates":56},"Point",[57,58],12.17128,45.89836,{"lat":58,"lon":57},[61,62,63],{"name":36,"role":41,"phone":42,"phoneExt":43,"email":44},{"name":36,"role":38,"phone":43,"phoneExt":43,"email":43},{"name":64,"role":65,"phone":43,"phoneExt":43,"email":43},"Leonardo Boccuni, Doctor of Philosophy","SUB_INVESTIGATOR",{"type":67,"investigatorFullName":43,"investigatorTitle":43,"investigatorAffiliation":43,"oldNameTitle":43,"oldOrganization":43},"SPONSOR","100569288","efficacy-of-stabilometric-platform-to-improve-standing-balance-in-patients-with-friedreichs-ataxia-100569288",false,"NCT06692296","Efficacy of Stabilometric Platform to Improve Standing Balance in Patients With Friedreich's Ataxia","Studio Pilota Sull'Efficacia Della Pedana Stabilometrica Nel Trattamento Del Paziente Con Atassia di Friedreich","Inclusion Criteria:\n\n* Age ≥ 14 years;\n* Weight \\\u003C 150 kg;\n* Genetic diagnosis of Friedreich's Ataxia;\n* Subscores of SARA (Scale for the Assessment and Rating of Ataxia) as follows: (1) from 1 to 6 for the item 'Gait (walking ability)'; (2) from 1 to 3 for the item 'Stance (ability to maintain a stable posture)'; (3) ability to walk ≥10 metres with or without walking aids; (4) ability to stand unsupported; Stadiation of the Friedreich Ataxia Rating Scale between 2 and 4.\n\nExclusion Criteria:\n\n* Age \\\u003C 14 years;\n* Diagnosis of acquired ataxia;\n* Subscores for items on the SARA scale of: (1) 0 or 7 for gait; (2) 0 or 4-6 for stance;\n* Inability to walk;\n* Ability to walk \\\u003C 10 meters;\n* Standing position possible only with support;\n* Other associated neurological conditions;\n* Current major psychiatric disorder (psychosis and major depression).","ALL","14 Years",{"count":78,"type":79},24,"ESTIMATED","INTERVENTIONAL",[82],"NA","The primary objective is to evaluate the potential effectiveness of an individualized intensive rehabilitation intervention using the \"Prokin 252\" stabilometric platform in the treatment of adolescent and adult patients with Friedreich's Ataxia. The secondary objective is to assess the retention of the rehabilitation treatment effects over time.\n\nEnrolled patients will be randomized and assigned to one of two treatment groups for four weeks. Three assessments will be conducted for each patient: one before treatment (T0), one at the end of treatment (T1), and a follow-up assessment 90 days after T1 via telemedicine (T2).\n\nThis study is:\n\n* Exploratory: The study aims to explore the usefulness of the stabilometric platform in a rehabilitative setting in combination with conventional therapy;\n* Not \"first-in-human\";\n* Longitudinal: The study will investigate changes over time in motor and functional ability scales, as well as stabilometric platform parameters, within the same cohort;\n* Randomized, controlled, open-label;\n* Monocentric: The study will be conducted only at the \"La Nostra Famiglia\" Association in Conegliano and Pieve di Soligo - IRCCS Eugenio Medea in Conegliano - UOC Neuromotor Rehabilitation in Pieve di Soligo, Via Monte Grappa, 96, 31053 Pieve di Soligo TV;\n* Prospective;\n* Post-market.",[85],"Friedreich Ataxia",[87,85,88,89,90,91,92,93,94,95,96,97,98,99],"randomized controlled trial","balance","rehabilitation","training","stabilometric platform","ataxia","therapeutic exercise","standing balance","Scale for the assessment and rating of ataxia","six minute walking test","functional reach test","timed up and go","Friedreich ataxia rating scale","2025-04-29",{"date":102,"type":103},"2025-05-02","ACTUAL",{"date":105,"type":103},"2025-02-03",{"date":107,"type":79},"2027-12",{"name":5,"class":6},1]