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Clinical Trial Summary

The purpose of this study is to study the effect mechanism of programmed flexor-extensor alternating electrical acupiont stimulation on upper limb functional reconstruction after stroke.


Clinical Trial Description

After being informed about the study and potential risks, all patients who meet the inclusion criteria, after signing the informed consent, will be randamized divided into two groups in a blind manner. The patients will undergo a 3-week treatment (6 days per week and 1 day for rest, a total of 18 days of treatment). Those in the control group are treated with conventional flexor-extensor alternating electrical acupiont stimulation, and in the treatment group, programmed stimulation will be adopted (30 minutes, once a day). Besides, data from healthy participants will be collected and processed for reference and control purposes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05333497
Study type Interventional
Source Heilongjiang University of Chinese Medicine
Contact
Status Completed
Phase N/A
Start date April 18, 2022
Completion date February 1, 2023

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