Shoulder-hand syndrome after stroke
Conditions
Interventions
Control group:Traditional rehabilitation therapy (active/passive movement training, acupuncture and moxibustion, ultrashort wave therapy)
Experimental group:Kinesio taping technique+Traditional rehabilitation therapy (active/passive movement training, acupuncture and moxibustion, ultrashort wave therapy)
Sponsors
Jiuquan Hospital of Shanghai First People's Hospital (Jiuquan People's Hospital)
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Shoulder-hand syndrome after stroke (hemorrhage or ischemia); 2. The course of disease within 1-3 months after stroke; 3. Age range: 18-80 years old; 4. Informed consent: patients or legal guardians signed informed consent to participate in the study voluntarily. 5. Be able to cooperate with the completion of relevant evaluation and treatment;
Exclusion criteria
Exclusion criteria: 1.Combined severe diseases: Combined with severe heart, liver and kidney dysfunction; Combined with malignant tumors or other serious systemic diseases; Combined with severe mental illness or cognitive dysfunction (MMSE<20 points); 2. Special groups: Pregnant or lactating women; Patients with an expected survival period of less than 6 months; 3. Past medical history: There is a history of diseases around the shoulder joint (such as periarthritis of the shoulder, rotator cuff injury, etc.); There is a history of fractures or surgeries on the same side of the upper limb in the past. There was previous peripheral neuropathy or brachial plexus nerve injury; 4. Therapeutic factors: Currently participating in other clinical trials; There are contraindications to the proposed treatment method; Has received surgical treatment for shoulder-hand syndrome; 5. Poor compliance: Inability to cooperate in completing the assessment and treatment plan; 6. Other factors: History of drug or alcohol abuse; patients expected to have difficulty in follow-up or may be lost to follow-up. Other circumstances that the researchers consider unsuitable for participation in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS for shoulder pain;ROM of the shoulder;Fugl-Meyer Assessment, FMA (Upper Limb); | — |
Secondary
| Measure | Time frame |
|---|---|
| The degree of hand swelling;VAS for hand pain;ROM of hand joints;Activities of Daily Living, ADL(Barthel index); | — |
Countries
China
Contacts
Public ContactYunan Lei
Jiuquan Hospital of Shanghai First People's Hospital (Jiuquan People's Hospital)
Outcome results
None listed