I60-I69
Conditions
Interventions
Group 1: Intervention group:
Study participants receive therapy sessions with the robotic device VEMOTION for 3 weeks. In the first week, 3 to a maximum of 5 VEMOTION therapies take place. In the rema
Sponsors
Schön Klinik Bad Aibling Harthausen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Admission to stroke unit or another neurological ward at the Schön Klinik Bad Aibling 45 kg = patient weight = 180 kg 150 cm < patient height < 195 cm Diagnosis: stroke (ICB/ischaemic) = 6 weeks Cooperative patients (according to the assessment of a non-study participating neurologist)
Exclusion criteria
Exclusion criteria: Severe contractures/ severe spasticity in the lower limb Presence of contraindications against mobilisation (decision taken by the attending physician) Diagnosis: Subarachnoid haemorrhage, transient ischaemic attack Pressure ulcer near the point of contact with the robotic device, on the back or buttocks Unstable fractures in areas relevant to therapy Severe aphasia Admission or stay in the ICU
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Ability to walk measuring using the Functional Ambulation Category (FAC) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Acute stroke assessment using the National Institutes of Health Stroke Scale (NIHSS). - Activities of daily living using the Barthel Index (BI) - Dependence in activities of daily living using the modified Rankin Scale (mRS) - Trunk control using the Trunk Control Test (TCT) - Balance using the Berg Balance Scale (BBS) - Muscle strength in the hip and knee extensors using the Medical Research Council Scale (MRC) - Transcranial Magnetic Stimulation (TMS) - Patient satisfaction with mobilisation - Patient-specific VEMOTION data: force and kinematic movement data | — |
Countries
Germany
Contacts
Public ContactAndreas Huber
f/p Design GmbH
Outcome results
None listed