cerebral stroke
Conditions
Interventions
Test Group (BCI-FES):Experimental Group (BCI-FES) : The patients were given electrode caps. For the first patients, the imagination threshold and the tolerated intensity of functional electrical stimu
Control Group (FES):Control group (FES) : Functional electrical stimulation was performed based on the tolerance level of the patients. Electrode location: The muscle belly of the total extensor phala
Sponsors
China Rehabilitation Research Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) It conforms to the cerebral blood of the Neurology Branch of the Chinese Medical Association and the Neurology Branch of the Chinese Medical Association in 2019 The diagnostic criteria for stroke were jointly formulated by the epidemiology group. At the same time, it was confirmed as cerebral infarction or cerebral hemorrhage through imaging examinations such as head CT or MRI, and it was the first onset with a disease course of no more than one month; (2) Patients with left hemiplegia have moderate to severe functional disorders in the affected upper limb and hand (Brumnstrom stage 1 and 2). (3) Mini-Mental State Examination (MMSE) > 21 points; (4) Patients or their families are clear about and understand the content of this study, possible risks and related risk handling, and voluntarily participate while signing the informed consent form. (5) The exercise intention questionnaire assesses the subjects' ability to execute mental images.
Exclusion criteria
Exclusion criteria: (1) Present with dementia: Mini-Mental State Examination (MMSE) score: Illiteracy <=17 points, severe hearing impairment, visual impairment, aphasia, etc., making it difficult to complete the training; (2) Patients with unilateral neglect; (3) Muscle, bone, and other neurological diseases that affect upper limb movement function, such as upper limb fractures, severe arthritis, and joint replacement surgery on the affected side; (4) There is a clear medical history of other causes of cognitive impairment, such as Alzheimer's disease, Parkinson's disease, etc. (5) Those with skin damage, infection or allergy to the electrode sheet at the contact site; (6) Those with metal implants, metal pacemakers or incomplete skulls in the brain.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl-Meyer Upper Limb Motor Function Assessment Scale;Action ResearchArm Test, ARAT;modified Barthel index, MBI; | — |
Secondary
| Measure | Time frame |
|---|---|
| modified Ashworth scale;Functional near-infrared spectroscopy;Sensory evaluation; | — |
Countries
China
Contacts
Public ContactJingya Liu
China Rehabilitation Research Center
Outcome results
None listed