I60 I61 I62 I63 I64
Conditions
Interventions
Group 1: For the intervention group, an individualized training plan for the SRT device-based circuit is developed by a qualified occupational therapist. The sessions are carried out under the supervi
Sponsors
MEDIAN Kliniken Unternehmenszentrale
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Primary diagnosis: Stroke within a maximum of three months after the event - Neurological rehabilitation phase C or D, including work-related medical rehabilitation - Nine Hole Peg Test (NHPT) > 30 seconds; if NHPT > 50 seconds, at least one peg must have been placed within that time - Ability to perform finger opposition up to the fourth digit - Sufficient cognitive and communication abilities to actively participate in therapy (including understanding of instructions and the ability to maintain attention for approximately 30 minutes) - Adequate vision to perform the exercises (with correction if necessary) - Written informed consent to participate in the study
Exclusion criteria
Exclusion criteria: - Severe impairment of the upper extremities: Marked limitation of shoulder mobility (shoulder abduction = 30°), Severe pain in the upper extremity (visual analogue scale = 6), Fixed contractures in the hand or forearm, Severe spasticity of the upper extremity Pronounced edema of the hand - Neurological and cognitive impairments: Severe neglect, clinically relevant apraxia - Presence of relevant comorbidities that prevent participation in the device-based training program
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in sensorimotor impairment of the affected upper extremity between baseline and the end of the intervention phase (approximately 3–4 weeks). Assessment is performed using the Fugl-Meyer Assessment for the upper extremity (FMA-UE). The change in the FMA-UE score is calculated as the difference between the baseline value (baseline measurement prior to the start of the intervention) and the value after completion of the intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Activity-related arm and hand function: Box and Block Test, Nine Hole Peg Test Activities of daily living: Barthel Index Walking ability: Functional Ambulation Category (FAC), 10-Meter Walk Test (10MWT) Work ability: Assessment of work ability at discharge Acceptance and experience parameters: Self-developed questionnaire | — |
Countries
Germany
Contacts
Public ContactLisa Happe
MEDIAN Unternehmenszentrale
Outcome results
None listed