Spasticity
Conditions
Interventions
A Group:conventional rehabilitation and Pestle needle
B Group:conventional rehabilitation and extracorporeal shock wave therapy
C Group:conventional rehabilitation,Pestle needle
control Group:conventional rehabilitation
Sponsors
Department of Rehabilitation Medicine,Shanghai Xuhui Central Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: (1) Voluntary participation, the subject can fully understand and cooperate and be willing to sign the consent form. If the subject is unable to sign the consent form due to hemiplegia, the legal guardian signs the informed consent form; (2) The first occurrence of stroke or previous lacunar infarction without sequelae; (3) Conform to the diagnosis of stroke in Diagnostic Points of Various Cerebrovascular Diseases adopted by the Fourth National Conference on Cerebrovascular Diseases in 1995, and showed a single infarction or hemorrhage on the side by CT or MRI. kitchen; (4) Unilateral hemiplegia, the MAS score of the hemiplegia was >1.5, and the muscle tension of the healthy limb was normal; (5) The recovery stages of arm motor function in stroke patients: Brunnstrom stage is III or IV. (6) The onset time of stroke was from 2 weeks to 12 mouths, Aged 18 to 80 years old, male or female, left or right, subjects with stable condition, clear consciousness, can tolerate sitting for 30 minutes and standing for 5 minutes;
Exclusion criteria
Exclusion criteria: 1. Patients who have Parkinson's disease and other high muscle tone; 2. Patients who have serious cognitive, verbal, visual, hearing or mental disorders and other effects of examination and treatment; 3. Patients who had a lacunar infarction and have sequelae; 4. Patients who have joint with disease (such as joint surgery or rheumatoid arthritis,etc.); 5.There are contraindications for electromyography or transcranial magnetic stimulation (such as epidermal damage, fever, etc.);and unable to tolerate the electromyography examination; 6.Participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| modified Ashworth scale;triple spasticity scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| F;H reflex; | — |
Countries
China
Contacts
Public ContactLijun Zhen
Department of Rehabilitation Medicine,Shanghai Xuhui Central Hospital
Outcome results
None listed