stroke
Conditions
Interventions
control group:Only routine rTMS treatment was given.
Stroke patients experimental group I:rTMS Stimulates Specific and Precise Localization of Brain Region 1
Stroke patients experimental group II:rTMS Stimulates Specific and Precise Localization of Brain Region 2
Stroke patients experimental group III:rTMS Stimulates Specific and Precise Localization of Brain Region 3
Sponsors
Department of Rehabilitation Medicine, Jiaxing Second Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Age range from 25 to 70 years; 2. First stroke; 3. Unilateral stroke; 4. Confirmed as swallowing disorder through swallowing imaging examination; 5. The rating of the Simplified Mental State Examination Scale is>=24 points; 6. Able to tolerate daily treatment doses; 7. Normal vision; 8. No contraindication of rTMS treatment (intracranial metal implant, implanted cardiac pacemaker, clear epilepsy history or epilepsy family history); 9. The course of the disease is 3-6 months.
Exclusion criteria
Exclusion criteria: 1. Non first-time stroke; 2. There are other diseases that affect the swallowing function of patients (such as neuromuscular junction, cranial neuropathy, muscle disease, digestive system disease, respiratory system disease, organic lesions in the oropharynx, esophageal disease, etc.); 3. Implantation of electronic devices and metal substances in the body (such as pacemakers, orthopedic internal fixation, etc.); 4. Mental and psychological disorders; 5. Unilateral spatial neglect exists; 6. Abnormal visual acuity test in ophthalmology; 7. Failure to cooperate with treatment; 8. Coma; 9. Severe cognitive impairment; 10. Severe aphasia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional Magnetic Resonance Imaging;Transcranial magnetic stimulation data;Behavioral data assessed by rehabilitation assessment scale; | — |
Countries
China
Contacts
Public ContactMing Zeng
Jiaxing Second Hospital
Outcome results
None listed