Clinical Study on the Effect of Corresponding Interactive Acupoint Selection on Hand Function During Ischemic Stroke
- Conditions
- Ischemic Stroke
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
1. The patients who have the history of stroke for the first time or have no sequelae meet the diagnostic criteria of ischemic stroke and have been confirmed by CT or MRI;
2. Those patients whose Brunnstrom classification of hemiplegic lateral hand function was II- IV;
3. Course of disease: 14 days to 3 months;
4. Patients aged 35-80 years, both male and female;
5. Patients with informed consent and signing informed consent.
1. Patients with other wrist and finger joint diseases;
2. The patients with mental disorder after stroke, such as those who are unable to answer questions or execute instructions due to coma or coma, or those who are seriously aphasia, have no speech or hearing comprehension ability;
3. Patients with severe cardiac insufficiency, severe liver and kidney dysfunction, hematopoietic system diseases and psychosis;
4. Pregnant or preparing pregnant women, lactating women.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Simplified Fugl-Meyer Motor Function Rating Scale (FMA) finger score;
- Secondary Outcome Measures
Name Time Method maximum grip strength of the affected hand;Improved Barthel Index;Measurement of hand joint mobility;