Skip to content

The efficacy of motor imagery-induced brain-computer interface technology combined with mechanical soft glove on upper limb function and cognitive function in left cerebral hemisphere injury

The efficacy of motor imagery-induced brain-computer interface technology combined with mechanical soft glove on upper limb function and cognitive function in left cerebral hemisphere injury

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092276
Enrollment
Unknown
Registered
2024-11-13
Start date
2024-11-20
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Left hemisphere damage

Interventions

hand routine rehabilitation group:The routine hand rehabilitation group was trained twice a day for 10 minutes and 30 minutes, 5 times a week, including joint range of motion training, muscle strength
Soft gloves group:On the basis of routine hand rehabilitation training once a day for 10 minutes, 5 times a week, the soft glove group conducted passive mechanical soft glove training for 10 minutes a
Brain computer interface Group:The brain-computer interface group was trained with the bionic software hand rehabilitation training system based on high-performance EEG-BCI five times a week and 10 mi

Sponsors

China Rehabilitation Research Center Beijing Boai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) age: 18-70 years old; (2) The patients were diagnosed as the recovery stage of stroke (left cerebral injury) by CT or MRI, and it was the first attack, and the course of disease was =MMSE=25).

Exclusion criteria

Exclusion criteria: (1) severe cognitive impairment or inability to pay attention to and understand screen information; (2) severe upper limb pain or spasticity, unable to perform normal hand training; (3) adherence is poor, cannot cooperate to complete the experiment; (4) has serious cardiovascular or respiratory system diseases; (5) unable to adhere to the study; (6) unwilling to participate in the study and sign informed consent.

Design outcomes

Primary

MeasureTime frame
Fugl Meyer assessment scale upper extremity;

Secondary

MeasureTime frame
Action Research Arm Test;modified Ashworth scale;Muscle tension function;Modified Barthel index;Montreal Cognitive Assessment Scale;Brain activation;Blood perfusion of the hands;

Countries

China

Contacts

Public ContactHuang Fubiao

China Rehabilitation Research Center

huangfubiao123@126.com+86 158 1031 1072

Outcome results

None listed

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