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Development and clinical application of a bionic soft body hand rehabilitation training system based on high performance EEG-BCI control

Development and clinical application of a bionic soft body hand rehabilitation training system based on high performance EEG-BCI control

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092509
Enrollment
Unknown
Registered
2024-11-18
Start date
2024-11-20
Completion date
Unknown
Last updated
2024-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral stroke

Interventions

hand routine rehabilitation group:Routine hand rehabilitation
Hand rehabilitation training system group:Passive mechanical soft glove training
Brain computer interface Group:Bionic software hand rehabilitation training system based on high-performance EEG-BCI

Sponsors

China Rehabilitation Research Center Beijing Boai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1: Patients with a first diagnosis of Right hemisphere damage (RHD) confirmed by CT or MRI 2: Onset was within 3 months 3: They are between 18 and 65 years old 4: Mini mental status examination (MMSE) score >17 5: The Brunstrom stage of the upper limbs and hands was stage I 6: The right hand is handedness 7: All participants signed informed consent prior to the study

Exclusion criteria

Exclusion criteria: 1: Hearing impairment, inability to communicate; Extreme restlessness or moderate to severe cognitive impairment inability to cooperate or inability to pay attention to and understand screen information 2: Medications affecting the central nervous system or other neuromodulation treatments are being used 3: Visual impairment, unilateral neglect, and inability to see the computer screen 4: Serious complications, heart and lung disease, uncontrolled hypertension, severe physical deformities, multiple organ damage or dysfunction of vital organs, severe spasms, etc 5: For patients with craniocerebral trauma and wound recovery period after craniocerebral surgery, electrodes cannot be placed or infected patients may be caused by brain electrode placement; Skull defect or skull repair with metal material; The inner body contains metal such as cardiac pacemakers 6: Patients with unhealed upper limb or hand fractures have left and right apraxia, joint contracture, and severely limited range of motion of the wrist and hand joints 7: Unwilling to sign informed consent

Design outcomes

Primary

MeasureTime frame
Fugl Meyer assessment scale (upper limb wrist hand part);

Secondary

MeasureTime frame
Fugl Meyer assessment scale (upper extremity);Sensory evaluation;modified Ashworth scale;Loewenstein Occupational Therapy Cognitive Assessment;Modified Barthel index;Brain activation;

Countries

China

Contacts

Public ContactFubiao Huang

China Rehabilitation Research Center

huangfubiao123@126.com+86 135 2271 8130

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026