I61 I63 I64
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: First ever Stroke (ICD: I61, I63, I64) NIHSS acute >0 Points Frühreha-Barthel-Index <30 points Clinical onset of symptoms in the last 72 hours
Exclusion criteria
Exclusion criteria: Subarachnoid hemorrhage (SAB), traumatic brain injury, hemorrhage into preformed cavities, other brain pathology significantly affecting prognosis (e.g., tumor, metastases). Other disease determining the prognosis (e.g., acute myocardial infarction, endocarditis, cancer, multiple sclerosis) Barthel index 30 points or above (thus not suitable for phase B) Planned surgical procedures in the next 3 months Cognitive impairment that makes informed consent impossible Death as a result of the disease up to T1 Lack of patient compliance Lack of informed consent from patient or relatives
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study is the motor function recovery after stroke, within the first 6 months of rehabilitation. For this purpose, a physical examination will be performed at three time points (T0, T1, T2). This includes the Fugl-Meyer Assessment and the following scales: Barthel-Index, NIHSS, mRS, FIM and FAM. T0 represents the time of study inclusion, here the patient is examined after consent on the stroke unit within the first 48 hours after stroke. T1 defines the time at the end of the early rehabilitation in the Department of Neurology, University Hospital Cologne. T2: represents the follow-up date after 6 months in the Polyclinic for Neurology, University Hospital Cologne. | — |
Secondary
| Measure | Time frame |
|---|---|
| Healtheconomic evaluation of rehabilitation after stroke, after 6 months | — |
Countries
Germany
Contacts
Klinik und Poliklinik für Neurologie, Uniklinik Köln