Stroke
Conditions
Interventions
BCI Group:On the basis of the control group, BCI training was administered. The treatment utilized a brain-computer interface rehabilitation training system. First, an electroencephalogram (EEG) cap w
Control Group:On the basis of the control group, conventional treatments were administered, including medication therapy, desktop cognitive rehabilitation therapy, motor therapy, psychotherapy, physic
BCI-TMS Group:Based on the BCI group, high-frequency (10Hz) repetitive transcranial magnetic stimulation (rTMS) was administered to the M1 area of the unaffected hemisphere.The patient was seated in a
Sponsors
The Fifth Affiliated Hospital of Zhengzhou University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Meet the diagnostic criteria for stroke of the Fourth National Cerebrovascular Conference in 1995, and it is the first stroke (ischemic stroke or hemorrhagic stroke, diagnosed by head CT or MRI), and the onset time is less than 6 months; 2. Aged 18-80 years old; 3. Hemiplegia and walking dysfunction after stroke; 4. Sitting balance >= grade 2; 5. Acceptable cognitive function, MMSE>=21, able to execute 2-step instructions; 6. Be able and willing to participate in the study.
Exclusion criteria
Exclusion criteria: 1. Severe cognitive impairment, aphasia, or mental instability; 2. Ankle joint instability, or contracture, fracture, arthritis and other orthopedic diseases; 3. Diagnosis of peripheral neuropathy or peripheral vascular disease, with symptoms that prevent or limit walking or participation in the study; 4. Weight >100kg, height outside the range of 150-188cm; 5. Patients with severe heart and lung diseases who cannot tolerate the test; 6. Visual, hearing, and vestibular organ dysfunction; 7. Patients with severe ataxia symptoms; 8. Exposure to infectious diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional Near-Infrared Spectroscopy;Fugl-Meyer Assessment;Action Research Arm Test;Montreal Cognitive Assessment;Hamilton Depression Rating Scale ;Motor Evoked Potential and Central Motor Conduction Time;Electroencephalogram data; | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse Event Rate;Modified Barthel Index;Kinesthetic and Visual Imagery Questionnaire;Wechsler Memory Scale;Attention Assessment; | — |
Countries
China
Contacts
Public ContactDong Anqin
The Fifth Affiliated Hospital of Zhengzhou University
Outcome results
None listed