stroke
Conditions
Interventions
Experimental group:True stimulation of the affected side of the M1 area - true stimulation of the cervical nerve root
Control group1:True stimulation of ipsilateral M1 area - sham stimulation of cervical nerve root
Control group2:Ipsilateral M1 area sham stimulation - cervical nerve root stimulation
Control group3:Ipsilateral M1 area sham stimulation - cervical nerve root sham stimulation
Sponsors
Tangdu Hospital, Air Force Military Medical University
Eligibility
Sex/Gender
All
Age
30 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. The initial onset, in line with the diagnostic criteria for stroke, unilateral lesions, confirmed by CT or MRI as hemorrhagic or ischemic lesions in the basal ganglia region; 2. Course of disease 2 weeks to 6 months, male or female, aged 30 to 80 years; 3. Be conscious and have stable vital signs at the time of enrollment; 4. There is upper limb dysfunction and Brunnstrom stage I to III of the upper limb on the affected side; 5. Willingness to take active rehabilitation and can cooperate with treatment instructions; 6. The patient and (or) authorized family members of the patient understand and sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Severe cognitive impairment or mental illness; 2. There is a metal foreign body in the skull; 3. Those with a history of epilepsy or a family history of epilepsy; 4. Those with pacemakers, stents and cochlear implants; 5. Those who cannot tolerate treatment; 6. Those with severe liver and kidney disease; 7. Those who cannot cooperate with the follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl-Meyer score;Wolf motor function test; | — |
Secondary
| Measure | Time frame |
|---|---|
| Brunnstrom evaluation of motor function in hemiplegia;Modified Barthel Index; | — |
Countries
China
Contacts
Public ContactLiu Rui
Tangdu Hospital, Air Force Military Medical University
Outcome results
None listed