I63 I61
Conditions
Interventions
Group 1: Intervention: combined training of 20 minutes cognitive training with NEUROvitalis HOME + 45 minutes of Motor therapy (physical/ occupational therapy)
Group 2: Control: combined training of 2
Sponsors
Klinik und Poliklinik für Neurologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: first ever stroke; maximum 7 days since stroke onset; no additional, relevant neurological or psychiatric disease; able to follow therapeutic instructions; able to understand and give informed consent
Exclusion criteria
Exclusion criteria: severe aphasia; severe vigilance reduction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cognition: General cognition and subfunctions (DemTect), processing speed, cognitive flexibility and exekutiv functionen (Trail Making Test A and B, TMTB/A), attention (Test of Attentional Performance, TAP-M, subtest alertness), reaction control (Test of Attentional Performance, TAP-M, subtest Inhibition) Motor function: bed mobility (Trunk Control Test), Balance (Berg Balance Scale), Hand function (Fist Closure Frequency) Functioning: ADL function (Functional Independence Measure), neurological status (National Institute of Health Stroke Scale) Timepoints: baseline (1 day prior to start of training) post training (1 day after end of training) | — |
Secondary
| Measure | Time frame |
|---|---|
| Age, gender, education, Vision, Hearing, time since onset of stroke, type of stroke, hemisphere and Region aphasia, neglect, mood, Level of activity before stroke, orientation | — |
Countries
Germany
Contacts
Public ContactMareike Gooßes
Uniklinik Köln, Medizinische Psychologie
Outcome results
None listed