Cerebral palsy / spina bifida / cranial nerve disease / spinal cord disease
Conditions
Interventions
rehabilitation
Sponsors
University of Tsukuba Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. A patient who can consent to a document by himself or his / her family. A substitute person is necessary. 2. Patient capable of wearing HAL. 3. During the study period, patients who can continue hospitalization or outpatient visits according to the study schedule.
Exclusion criteria
Exclusion criteria: 1. Patients who have difficulty in voluntary limb activity according to instructions due to consciousness disturbance or severe dementia. 2. Patients who are severely deformed in the skeletal system such as osteoarthritis, degenerative spondylosis, scoliosis, and are difficult to train including joint movement. Patient who is difficult to wear HAL. 3. Patients who have complications such as bleeding tendency or osteoporosis which are problems in training. 4. Patients who can not affix HAL biomedical electrodes due to skin diseases. 5. Patients who participated in other research within 12 weeks of this clinical study. 6. Clinical trial Patients who are judged to be inappropriate for participation in this study by a physician or shared medical doctor.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse event Malfunction of HAL and accessory equipment Feasibility of rehabilitation | — |
Countries
Japan
Contacts
Public ContactHiroshi KAMADA
University of Tsukuba Hospital Department of Orthopaedics surgery
Outcome results
None listed