Children and young adults with neurologic gait disorders G80 P10 P11 S06 I63 C71 D33 Q05
Conditions
Interventions
Group 1: Participating patients will undergo a minimum of one and a maximum of two therapy sessions during which physiological recordings will be collected for therapy goal dependent alterations of Lo
Sponsors
Kinderreha Schweiz - Universitätskinderspital Zürich
Eligibility
Sex/Gender
All
Age
5 Years to 25 Years
Inclusion criteria
Inclusion criteria: English: - Informed consent signed by the subject and/or the legal representative - 5-25 years - Healthy or a record of neurological gait disorder
Exclusion criteria
Exclusion criteria: English: - Inability to communicate pain and discomfort - Inability to follow the study instructions - Other factors that prevent the usage of the Lokomat
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| English: Primary Outcome are the therapist chosen Lokomat training parameter for 2 different intensity levels. They will be collected with the device during the therapy. The goal is to cluster them and relate the clusters to clinical patient characteristics and physiologic reactions during the therapy. | — |
Secondary
| Measure | Time frame |
|---|---|
| English: physiologic recordings (sEMG, kinematic gait pattern, heart rate) Deutsch: | — |
Countries
Switzerland
Contacts
Public ContactRob Labruyère
Kinderreha Schweiz - Universitätskinderspital Zürich
Outcome results
None listed