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Effect of brain-muscle interface training equipment based on motor imagination on upper limb functional rehabilitation of stroke patients

Effect of brain-muscle interface training equipment based on motor imagination on upper limb functional rehabilitation of stroke patients

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056911
Enrollment
Unknown
Registered
2022-02-22
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Stoke

Interventions

The control group:Motomed upper limb equipment training
The experimental group:Brain-computer interface upper limb rehabilitation equipment training

Sponsors

The First Affiliated Hospital of Nanjing Medical University (Jiangsu Province Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. It conforms to the diagnostic criteria of cerebral apoplexy in Chinese Classification of Cerebrovascular Diseases in 2015; 2. First stroke, 1 month = course =6 months; 3. 18-80 years old; 4. The lesions were only in one cerebral hemisphere; 5. There was no significant cognitive impairment, and the score of simplified mental state examination was =21; 6. Improved Ashworth: upper limb muscle =1+; 7. The ability to perform motor imagination task was assessed by motor and visual imagination questionnaire; 8. Informed consent signed by the patient himself or his immediate family member.

Exclusion criteria

Exclusion criteria: 1. Patients with unstable stroke condition, or complicated with serious heart, lung, liver, kidney and other important organ diseases could not complete the experiment 2. patients with epilepsy or have been diagnosed as secondary epilepsy; 3. with severe visual impairment, hearing impairment, complete aphasia, unable to understand and complete the training; 4. Patients with obvious shoulder pain or other diseases, such as unstable fracture, infection or active bleeding of the upper limb or hand, that lead to failure to complete the training; 5. Unable to cooperate with patients with poor treatment compliance; 6. Patients diagnosed with transient ischemic attack (TIA) or reversible ischemic neurological dysfunction (RIND); 7. Participated in clinical trials of other drugs or medical devices in the same period.

Design outcomes

Primary

MeasureTime frame
The Fugl-Meyer Upper Extremity Scale;

Secondary

MeasureTime frame
Modified Barthel index;Simple upper limb function assessment;Surface emG assessmen;Functional near infrared spectroscopy;

Countries

China

Contacts

Public ContactYongqiang Li

The First Affiliated Hospital of Nanjing Medical University (Jiangsu Province Hospital)

liyongqiang_1980@163.com+86 13327829260

Outcome results

None listed

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