Overview
After the selected patients are determined, the researchers of this study need to have full communication with the patients. The location is the rehabilitation ward of our hospital and the time is
Before joining the group. During this process, the patient should be informed of the purpose, procedures and processes of the trial. The informed consent form should be signed by the patient himself/herself. Such as the patient
Illiterate, the informed consent process was witnessed by an independent witness and signed. The subject pressed their fingerprint at the signature. In the study process fully
Listen to and respond to the questions and opinions of the subjects or their representatives.
Eligibility
Inclusion Criteria:
- It meets the diagnostic criteria of the "Guidelines for the Prevention and Treatment of Cerebrovascular Diseases in China", and is diagnosed as cerebral infarction or cerebral hemorrhage by CT or MRI.
- The first stroke occurred;
- The muscle strength of the flexor and extensor muscles of the affected finger is ≤ grade 1.
- Right-handed player
- Muscle tone improvement: Asworth level 2 or below;
- The disease course is within 6 months and the condition is stable.
- Age: 18 to 75 years old, with normal vision and hearing or corrected to normal.
Exclusion Criteria:
- Those with an MMSE score less than 20, severe memory, communication and speech command comprehension disorders, and those who cannot cooperate with examinations and treatments;
- Those with a history of epilepsy;
- Those with a history of stroke, traumatic brain injury or brain tumor in the past;
- Those with peripheral nervous system injuries other than stroke as diagnosed by imaging;
- Those with visual spatial impairments such as visual field defects and unilateral neglect;
- Skull defect or metal bone plates
- For those who are not suitable for functional near-infrared examination;
- Those with a history of intracranial surgery.
- Patients with lesion areas in the cerebellum or brainstem.
