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ERD/ERS-dynamic network research of enhanced EEG-BCI on modulating LI of symmetrical brain regions and promoting motor recovery

ERD/ERS-dynamic network research of enhanced EEG-BCI on modulating LI of symmetrical brain regions and promoting motor recovery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068400
Enrollment
Unknown
Registered
2023-02-17
Start date
2023-02-17
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

stroke

Interventions

Group A:EEG-BCI
Group B:sham EEG-BCI
Group C:enhanced EEG-BCI

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) First stroke; (2) Unilateral subcortical injury; (3) Stroke confirmed by computed tomography (CT) or MRI and the diagnosis was in line with the consensus on the Diagnosis of Various major cerebrovascular diseases in China 2019 formulated by the Cerebrovascular Group of the Chinese Society of Neurology; (4) more than 2 weeks and less than 6 months after onset; (5) There was upper limb and hand motor dysfunction, Fugl-Meyer scale motor function score wrist-hand part < 24 points; (6) 18 years old = age = 65 years old; (7) No cognitive impairment, mini-mental state examination (MMSE) = 25 points.

Exclusion criteria

Exclusion criteria: (1) Patients with severe heart, lung, liver, kidney and other important organ failure in the past, uncontrolled hypertension, arrhythmia, severe coronary heart disease, diabetes complications with poor control; (2) have a history of seizures or family history of epilepsy; (3) intracranial or external metal; (4) the body is equipped with medical equipment, such as cardiac pacemaker, drug pump, etc.; (5) Unable to complete the basic course of treatment, poor compliance; (6) pregnant women; (7) Participants who have recently participated in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Motor Assessment;

Secondary

MeasureTime frame
Modified Ashworth Assessment;modified Tardieu Scale,MTS;Action Research Arm Test,ARAT;Box and Blocks Test,BBT;Wolf motor function test,WMFT; Activity of daily living score (Modified Barthel index);EEG;

Countries

China

Contacts

Public ContactShugeng Chen

Huashan Hospital, Fudan University

tonychshug@126.com13501959548

Outcome results

None listed

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