Measurement of the individual reactions to Adaptions of Lokomat Parameters
Not Applicable
Recruiting
- Conditions
- G80P10P11S06I63C71D33Q05Cerebral palsyIntracranial laceration and haemorrhage due to birth injury
- Registration Number
- DRKS00027251
- Lead Sponsor
- Kinderreha Schweiz - Universitätskinderspital Zürich
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
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
English:
- Inability to communicate pain and discomfort
- Inability to follow the study instructions
- Other factors that prevent the usage of the Lokomat
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method English:<br>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.<br>
- Secondary Outcome Measures
Name Time Method English:<br>physiologic recordings (sEMG, kinematic gait pattern, heart rate)<br>Deutsch: