Stroke with unknown ischemia or hemorrhage
Conditions
Interventions
Conventional Intervention Group:A 4-week program of standard conventional rehabilitation therapy, administered 5 times per week, including therapeutic positioning, exercise therapy, occupational thera
Mirror therapy group:A 60 cm × 50 cm medical-grade shatterproof mirror was placed vertically on the tabletop. The patient was seated in a comfortable position with the non-paretic arm positioned in fr
Robot-assisted glove group:The Yisheng SY-HR06 pneumatic upper limb rehabilitation robotic glove was used. The patient selected an appropriately sized glove and utilized the "passive therapy" mode (in
Robot-assisted glove combined with mirror therapy group:In addition to conventional therapy, the interventions described above (mirror therapy and robotic glove training) were administered concurrentl
Sponsors
Wuhan Wuchang Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Age 18-80 years (inclusive). 2. Diagnosed with first-ever ischemic or hemorrhagic cerebral hemisphere stroke by CT or MRI. 3. Onset time between 1 and 6 months (subacute phase). 4. Presence of clear unilateral upper limb hemiplegia. 5. Right-handed before the stroke. 6. Mini-Mental State Examination (MMSE) score >=24, no severe aphasia or comprehension disorder, able to follow study instructions. 7. Voluntarily participate and sign the written informed consent form.
Exclusion criteria
Exclusion criteria: 1. History of other neurological diseases (such as Parkinson's disease, multiple sclerosis, etc.); 2. MRI shows cortical infarction in both cerebral hemispheres or lesions located in the cerebellum or brainstem; 3. Presence of contraindications for fNIRS detection (such as local scalp infection, melanoma, skull defect >3 cm); 4. Combined severe dysfunction of organs such as heart, lungs, liver, or kidneys (e.g., New York Heart Association [NYHA] cardiac function class III-IV); 5. Currently participating in other clinical trials that may affect upper limb function rehabilitation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl-Meyer Upper Extremity Motor Function (FMA-UE);Motor evoked potential (MEP); | — |
Secondary
| Measure | Time frame |
|---|---|
| change in Oxyhemoglobin Concentration;Practical Function of the Upper Limb;Modified Barthel Index;Hand Function Subdomain of the Stroke Impact Scale (SIS);Mini-Mental State;Visual Analog Scale Score;Functional Independence ;Changes in oxygenated hemoglobin concentration measured by functional near-infrared spectroscopy (fNIRS-?HbO);Electroencephalography (EEG) indicators; | — |
Countries
China
Contacts
Public ContactTangzhu Yang
Wuhan Wuchang Hospital
Outcome results
None listed