* Objective assesment of the feasibility of integrating the Ekso Bionics - Ekso NR device into outpatient care * Objective assesment of quality of life, functionality and clinical symptomps of patients with stroke, cerebellar ataxia, spinal cord injury, and spastic paraparesis * Comparison of measured data and follow-up of changes in relation to themselves and each other * Analyzing the effects of the exoskeleton among the patients * Assessing the safety, possible side effects and tolerability of the EksoNR
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Functional Independence Measure (FIM)
Timeframe: 4 weeks
Barthel Index (BI)
Timeframe: 4 weeks