I60 I61 I62 I63 I64
Conditions
Interventions
Group 1: At one point, passive training is conducted with the patients.
Group 2: At the other time, active training is carried out with the patients.
Sponsors
Lurija Institut Kliniken Schmieder Allensbach
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Ability to give informed consent to participate in the study 2. Sufficient understanding of the task 3. No or minor pain in the affected arm, measured by visual analog scale 4. First stroke (ischemia or hemorrhage), not longer than 6 months ago 5. Rehabilitation phase C or D 6. Paresis of the upper extremity with a strength level of 3 to 4
Exclusion criteria
Exclusion criteria: 1. Cognitive impairments that do not allow information about the study (e.g. Wernicke's aphasia, global aphasia, dementia) 2. Warticipants with a lack of compliance 3. Pain 4. Participants with electronic implants (e.g. pacemakers) 5. Epilepsy 6. Pregnancy 7. Intracranial metal particles (e.g. vascular clips)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Transcranial magnetic stimulation: single stimulus amplitudes, short- and longlatency intracortical inhibition, intracortical facilitation, cortical silent periode | — |
Secondary
| Measure | Time frame |
|---|---|
| Box-and-block test | — |
Countries
Germany
Contacts
Public ContactJoachim Liepert
Kliniken Schmieder Allensbach
Outcome results
None listed