stroke
Conditions
Interventions
Intervention group:Mirror therapy based on active sensorimotor task
Control group:Conventional active sensorimotor tasks
Sponsors
Huashan Hospital Fudan University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18-80 years, right-handed, with normal vision or corrected vision; 2. The first and unilateral cerebral hemorrhage/cerebral infarction was confirmed by computed tomography (CT) or magnetic resonance imaging (MRI); 3. The diagnosis was in line with the standard of Diagnostic Essentials of Major Cerebrovascular Diseases in China 2019 formulated by the Cerebrovascular Disease Group of the Neurological Branch of the Chinese Medical Association; 4. The onset time was 1 week to 6 months, and the condition was stable; 5. No cognitive impairment, MoCA score >= 22, can cooperate with evaluation and treatment; 6. First accepted mirror image therapy; 7. Brunnstrom stage of upper limb and hand is between stage I and stage IV, and the major flexors of wrist and elbow are not accompanied with severe spasm, including the muscle tension of wrist flexors and biceps brachii <= 2 (modified Ashworth scale); 8. Patients can be kept in a sitting position for at least 60 minutes; 9. Volunteer to participate in this study, and sign the informed consent form by himself or his immediate family on behalf.
Exclusion criteria
Exclusion criteria: 1. The condition worsens, with new infarct or large area cerebral infarction; 2. Previous history of epilepsy, cerebral hemorrhage, severe heart, lung, liver, kidney and other important organ failure, uncontrolled hypertension, arrhythmia, severe coronary heart disease, and poor control of diabetes complications; 3. Other central nervous regulation technologies, such as brain computer interface technology, transcranial electrical stimulation technology, motor imagination therapy and other intervention tests are being conducted; 4. Those who are allergic to conductive paste, scrub paste and other test related equipment and components; 5. Contraindications of neuroelectrophysiological examination and magnetic resonance examination, such as claustrophobia, wearing a cardiac pacemaker, intracranial metal implants or skull defects, pregnancy, lactation, or childbearing women without reliable contraceptive measures; 6. Those who cannot complete the test and have poor compliance.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl - Meyer Upper Limb Motor Function Assessment Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Box and Block Test;Action Research Arm Test;Modified Barthel Index;Functional Independence Measure;Brunnstrom Stage;Grip Strength Test;Pinch Strength Test;Modified Ashworth Scale;Somatosensory Evoked Potentials;Electroencephalogram;Magnetic Resonance Imaging;Fugl-Meyer Upper Extremity Sensory Function Assessment Scale;2-Point Discrimination Test;Semmes Weinstein Monofilament; | — |
Countries
China
Contacts
Public ContactJie Jia
Huashan Hospital, Fudan University
Outcome results
None listed