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Study on the mechanism and application of neurovascular coupling in stroke patients based on EEG-fNIRS multimodality

Study on the mechanism and application of neurovascular coupling in stroke patients based on EEG-fNIRS multimodality

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089065
Enrollment
Unknown
Registered
2024-08-30
Start date
2024-08-31
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

stroke

Interventions

Healthy group :Perform activities of daily living
stroke group:Perform activities of daily living

Sponsors

kunming medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Stroke group: ? The patient was diagnosed for the first time and met the diagnostic criteria of stroke in the Chinese Guidelines for the Prevention and Treatment of Cerebrovascular Diseases. Cerebral vascular lesions were confirmed by head CT or MRI examination. Hemiplegia. ? Gender is not limited, age 18-70 years old, right-handed, disease duration not more than 2 years. ? No serious cognitive impairment, able to understand the experimental instructions (MMSE>21 points); Sitting balance =2, Brunstorm stage =III. ? control group ? Unknown neurological and osteoarthritic diseases. ? Gender is not limited, age 18-70 years old; Right-handed. ? No history of major surgery in the past 2 years, no recent history of upper limb trauma.

Exclusion criteria

Exclusion criteria: ? Exclusion criteria: ? hemiplegic side limb fracture, serious infection, shoulder periarthritis and other upper limb bone and joint diseases and malformations, upper limb pain; ? Unstable condition, history of epilepsy; Corrected vision less than 5.0; Hearing and speech impairments affect communication. ? head skin infection or damage, skull insufficiency, intolerance of fNIRS, EEG; A history of mental illness or any antipsychotic medication not appropriate for this study. (2) No special population was included in this study, and the intervention process included upper limb robot and routine rehabilitation treatment, which were provided by occupational therapists with more than 3 years of treatment experience, and the intervention was non-invasive, and any discomfort or fatigue during the treatment could be terminated or suspended at any time.

Design outcomes

Primary

MeasureTime frame
fNIRS;EEG;FMA;

Countries

China

Contacts

Public Contactxu xuan

kunming medical university

1228458748@qq.com+86 183 1445 8950

Outcome results

None listed

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