Functional Electrical Stimulation (FES) and Reconstructive Tetraplegia Hand and Arm Surgery (FES)
Spinal Cord Injury Cervical
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About this trial
This is an interventional treatment trial for Spinal Cord Injury Cervical focused on measuring Functional Electrical Stimulation, Tetraplegia, Reconstructive Hand Surgery
Eligibility Criteria
Inclusion Criteria:
- traumatic or non-traumatic (> 6 month) spinal cord injury
- Age ≥ 18 years
- Level of lesion C4 - Th1
- American Spinal Cord Injury Association Impairment Scale (AIS) A/B/C/D
- Planned reconstructive hand or arm surgery at the Swiss Paraplegic Centre Nottwil
- Signed informed consent
Exclusion Criteria:
- Patients during primary rehabilitation
- Patients' inability to follow the study, e.g. mental-health problems, language problems, dementia etc.
- Pregnancy (anamnestic)
Sites / Locations
- Swiss Paraplegic CentreRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Functional Electrical Stimulation
Standard therapy
Before surgery, the donor muscle is stimulated via surface electrodes in a loaded position or against resistance 3 times a week for 30 minutes. After surgery, the patients receive the same standard therapy as the control group. The electrical stimulation is performed once a day in combination with standard therapy for 30 minutes against gravity or resistance or in a loaded position.
Postoperatively, 20 min passive and active movements of the hand or arm are applied manually by a therapist. Additionally, the patients actively perform the same exercises once a day for 20 min. The movements are based on a standardised post-surgical treatment protocol.