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Development and clinical application of MI-BCI- soft hand rehabilitation robot for spinal cord injury

Development and clinical application of MI-BCI- soft hand rehabilitation robot for spinal cord injury

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091581
Enrollment
Unknown
Registered
2024-10-30
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

spinal cord injury

Interventions

control group:Routine occupational therapy training: The control group received 30min/ time, 2 times/day and 5 times/week of routine operational treatment training, including joint motion training, mu
Soft exoskeleton group:Passive soft exoskeleton training: On the basis of routine hand rehabilitation training once a day and 5 times a week, the soft exoskeleton group received passive soft exoskelet
Brain computer interface Group:Training of MI-BCI- Soft hand rehabilitation robot for spinal cord injury: The brain computer interface group received 30min/ week training of MI-BCI- soft hand rehabili

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)The patient was diagnosed with C5-C7 spinal cord injury by imaging 2)ASIA is graded B, C and D 3)They are between 18 and 65 years old 4)Modified Ashworth scale grade of hand =2 5) Able to remain seated for =30 minutes 6)Have certain motor imagination ability 7)All participants signed informed consent prior to the study

Exclusion criteria

Exclusion criteria: 1)Having a disease that affects hand motor function and recovery process 2)A metal implant, a metal pacemaker, or an incomplete skull 3)MMSE score < 21 points, have serious cognitive impairment 4)Hearing impairment, unable to communicate, unable to cooperate with the experiment 5)There are contraindications for BCI/soft exoskeleton /fNIRS 6)Also participate in other clinical research trials

Design outcomes

Primary

MeasureTime frame
Action Research Arm Test;

Secondary

MeasureTime frame
Active Range of Motion;grip strength;Modified Ashworth Scale;spinal cord independence measure III;Brain function;

Countries

China

Contacts

Public ContactJingya Liu

China Rehabilitation Research Center

jealousy313@163.com+86 158 0153 0159

Outcome results

None listed

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