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The synergistic efficacy of motor imagery-based brain-computer interface combined with modified constraint-induced movement therapy on upper extremity function in stroke patients

The synergistic efficacy of motor imagery-based brain-computer interface combined with modified constraint-induced movement therapy on upper extremity function in stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124103
Enrollment
Unknown
Registered
2026-05-07
Start date
2025-12-24
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Stroke

Interventions

Combined group:Brain-computer interface combined with modified constraint-induced movement therapy
Control group:modified constraint-induced movement therapy alone

Sponsors

Xuzhou Rehabilitation Hospital Affiliated to Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age between 18 and 75 years; 2.First-ever stroke; 3.Unilateral lesion with a disease duration of less than 6 months and stable vital signs; 4.Fulfillment of the training criteria for mCIMT in stroke patients: active wrist extension of the affected upper extremity exceeding 20°, active extension of the thumb and at least two additional fingers at the metacarpophalangeal and interphalangeal joints exceeding 10°, performed at least three times per minute ; and passive range of motion meeting the following requirements: shoulder flexion and abduction exceeding 90°, elbow extension exceeding 30°, and both forearm pronation and supination exceeding 45°; 5.Modified Ashworth Scale grade for flexor muscle tone in the upper limb <= II; 6.Mini-Mental State Examination score of 21 or higher, with intact consciousness and adequate cognitive function to cooperate with evaluation and treatment; 7.Absence of auditory or visual impairments.

Exclusion criteria

Exclusion criteria: 1.Presence of traumatic brain injury, progressive stroke, or subarachnoid hemorrhage with an unstable clinical condition; 2.Comorbid severe cardiac, hepatic, pulmonary, or renal insufficiency, malignancy, psychiatric trauma, or cognitive dysfunction; 3.Use of implanted electronic devices (such as cardiac pacemakers) or presence of metallic implants (such as stents); 4. Personal or family history of epilepsy; 5.Poor treatment compliance precluding completion of the trial; 6. Severe pain, sensory loss, hyperesthesia, or other sensory impairments affecting the hemiplegic limb.

Design outcomes

Secondary

MeasureTime frame
Wolf Motor Function Test;modified Barthel Index;

Primary

MeasureTime frame
Fugl-Meyer Assessment for Upper Extremity;

Countries

China

Contacts

Public ContactWenjie Zhou

Xuzhou Rehabilitation Hospital Affiliated to Xuzhou Medical University

1157499040@qq.com+86 187 5211 7782

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026