Effect of Overground Gait Training Using a Torgue-Assisted Exoskeletal Wearable Device on Ambulatory Function in Subacute Stroke Patients
Subacute Stroke
About this trial
This is an interventional treatment trial for Subacute Stroke
Eligibility Criteria
Inclusion Criteria
- patients with significant difficulty in communication, such as severe cognitive impairment (MMSE <10) or speech-language impairment
- patients with ataxia
- patients with spasticity of the affected lower extremity of measured by Modified Ashworth scale (Modified Ashworth Scale (MAS) ≥ 2)
- patients with severe musculoskeletal disorder in the lower limbs
- patients with a contracture that limits the lower limb range of motion
- patents with apparent leg length discrepancy of 2 cm or more (Rt: cm / Lt: cm)
- patients with a lower limb fracture or open wound or unhealed ulcer
- patients to whom robot-assisted gait rehabilitation cannot be applied due to a severe cardiovascular or pulmonary disease
- patients with a history of osteoporotic fracture
- patients with a neurological disorder that may affect the ambulatory function (e.g. Parkinson disease, multiple sclerosis, etc.)
- patients determined to be ineligible by the investigator
Exclusion Criteria
- patients who express a desire to drop out of treatment
- patients who do not comply with the guidelines provided by the investigator
- patients who require a treatment outside the scope of the present clinical study
- patients who show a severe injury due to an accident such as a fall
- patients who participate in < 80% of training sessions
- patients who show a new major condition and consequently require absolute rest for recovery (e.g. another incidence of stroke, aggravation of stroke, myocardial infarction, any other neurological, internal, or musculoskeletal condition, etc.)
Sites / Locations
- Yonsei University Health System, Severance HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Robot-assisted Training Group
Control Group
- After the baseline test, the training is performed with 20 sessions in total (60 min / session); five sessions a week for four weeks. The robot-assisted training group is given 30 min conventional gait training and another 30 min (excluding robot attachment and detachment time) gait training using an exoskeletal wearable robot, while the control group is given 1 hr conventional gait training for the same time as the robot-assisted training group. In all participants in each group, no other robot-assisted rehabilitation such as Lokomat, Erigo, or Morning Walk could be performed.
- After the baseline test, the training is performed with 20 sessions in total (60 min / session); five sessions a week for four weeks.