I61 I63 I69.4 G82 R54
Conditions
Interventions
Group 1: People will wear XoSoft prototypes and will anwer questions to the basic functionality of the prototypes and the movement pattern during daily activities will be recorded. For each arm, 3 peo
Sponsors
Zürcher Hochschule für Angewandte Wissenschaften
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: body mass index: 20-28 kg/m2 Mini Mental State Examination score > 24 Signed informed consent unilateral impariment (for patients) for stroke patients: main diagnosis: chronic stroke (>6 months); FAC score 3-5 for incomplete spinal cord injury: main diagnosis_ incomplete spinal cord injury (>6 months); FAC score 3-5 for frailty: 2 positive criteria for frailty phenotype, FAC score 3-5
Exclusion criteria
Exclusion criteria: acute musculoskeletal, cardiopulmonary, neurological diseases amputations for patients: excessive spasticity, joint mobility restrictions in the lower limbs that interfere with daily locomotion, pain, inability to wear prototype lower limb exoskeleton
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is a written report on the basic functionality of the prototype lower limb exoskeleton. Basic functionality will be assessed using qualitative and quantitative questionnaires about functionality, usability, perceived exertion and local pressure that will be answered by the study participants. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are the differences in kinematics, kinetics and muscle actitivy of the lower extermities with and without the prototype | — |
Countries
Switzerland
Contacts
Public ContactCarole Pauli
Zürcher Hochschule für Angewandte Wissenschaften
Outcome results
None listed