Condition: Neuromotor Impairments · Sponsor: IRCCS Fondazione Stella Maris
The goal of this clinical trial is to demonstrate the efficacy of multi domain robotic and technological rehabilitation on everyday life and satisfaction in children with neuromotor conditions. The main questions it aims to answer are: * Will we have significant changes using the COPM in children taking part in the sperimental group? * The children who will undergo the multidomain treatment will also experience functional improvements in individual areas? * Thy type of treatment will improve motivation, active participation and satisfaction in children? Researcher will compare the multidomain treatment to standard care proposed by the included clinical centers: single domain rehabilitation with one innovative device. Both groups will undergo also conventional multidomain therapy. This will be done to see if using a holistic approach, and including every need of the child in the rehabilitation plan, can lead to greater improvements in quality of life compared to the control group. Participant will: * Be evaluated 3 times with clinical outcome measures * Take part in a rehabilitation program, at least 20 x 2hours sessions treatment, organized in: * 4 weeks, 5 times per week * 7 weeks, 3 times per week
This description comes directly from the study's public registry record.
Giuseppina Sgandurra Prof.ssa Sgndurra · 050886284 · giuseppina.sgandurra@fsm.unipi.it
Always discuss trial participation with your own doctor first.
| IRCCS Giannina Gaslini | Genova, Genova, Italy | Not Yet Recruiting |
| IRCCS Eugenio Medea | Bosisio Parini, Lecco, Italy | Recruiting |
| Fondazione Don Gnocchi IRCCS centro "Santa Maria Nascente" | Milan, Milano, Italy | Not Yet Recruiting |
| IRCCS Istituto Neurologico Naz.le C.Mondino | Pavia, Pavia, Italy | Not Yet Recruiting |
| IRCCS Fondazione Stella Maris | Calambrone, Pisa, Italy | Not Yet Recruiting |
| Fondazione Don Gnocchi IRCCS centro "S.Maria al Mare" | Salerno, Salerno, Italy | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT06666829