brachial plexus injury
Conditions
Interventions
Part ?: Group 1 (Group of patients with brachial plexus injury):In part I, no intervention is performed, and simultaneous acquisition of electroencephalographic (EEG) and electromyographic (EMG) signa
Part I: Group 2 (Healthy control group):In part I, no intervention is performed, and simultaneous acquisition of electroencephalographic (EEG) and electromyographic (EMG) signals is conducted during v
Part II: Group 1 (Experimental group):Conventional rehabilitation treatment combined with the brain-muscle-machine Interface rehabilitation training system treatment.
Part II: Group 2 (Control group):Conventional rehabilitation treatment
Sponsors
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine
Eligibility
Sex/Gender
All
Age
12 Years to 70 Years
Inclusion criteria
Inclusion criteria: The inclusion criteria for healthy subjects: 1. Aged >=12 years and =12 years and <=70 years, regardless of gender. 4. Right-handed. 5. Detectable electromyographic signals in forearm muscles as confirmed by neurophysiological examination. 6. Capable of understanding, agreeing to participate in the study, and signing the informed consent form.
Exclusion criteria
Exclusion criteria: The exclusion criteria for healthy subjects: 1. Individuals who have participated in or are actively participating in another clinical research study within one month prior to enrollment. 2. Pregnant or lactating women. The exclusion criteria for patients with brachinal plexus injury: 1. Patients with central nervous system injuries. 2. Presence of contraindicated neuroregulation implants (e.g., ferromagnetic implants, pacemakers). 3. History of epilepsy, psychiatric disorders, or other severe cognitive or emotional dysfunctions. 4. Other conditions affecting limb movement, such as fractures, severe arthritis, amputation. 5. Malignant tumors (primary or metastatic) in the repaired nerve or surrounding tissues. 6. Severe cardiopulmonary insufficiency or serious primary diseases affecting the liver, kidneys, hematologic, or endocrine systems. 7. Pregnant or lactating women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Action Research Arm Test; | — |
Secondary
| Measure | Time frame |
|---|---|
| Disabilites of the arm,shoulder,and hand;Manual Muscle Test;Range of motion;Minimum Mental State Examination; The British Medical Research Council (BMRC) scale for sensory recovery;Numerical Rating Scale,NRS;Hamilton Anxiety Scale,HAMA;Hamilton Depression Scale;Electromyography,EMG;Electroencephalogram,EEG;Corticomuscular coherence,CMC; | — |
Countries
China
Contacts
Public ContactJiajia Wu
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai
Outcome results
None listed