Stroke
Conditions
Interventions
Control Group:onventional Cognitive Training: 15 min/session, twice daily, 5 days/week for 4 weeks
Conventional Occupational Therapy: 30 min/session, once daily, 5 days/week for 4 weeks.
Experimental Group:Eye-Tracking Cognitive Rehabilitation: 15 min/session, once daily, 5 days/week for 4 weeks
Conventional Cognitive Training: once daily, 5 days/week for 4 weeks
Sponsors
China Rehabilitation Research Center
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Eligibility Criteria (1)Patients with first-ever right hemisphere lesions diagnosed with cerebrovascular disease in accordance with the diagnostic criteria established at the 4th National Academic Conference on Cerebrovascular Diseases, confirmed by CT or MRI; (2)1 to 6 months after stroke onset with stable medical condition; (3)Aged 18 to 70 years old; (4)Educational level of junior high school or above; (5)Ability to maintain independent sitting position for >=30 minutes; (6)Montreal Cognitive Assessment (MoCA) score of 18 to 26 points with attention subscore < 6 points; (7)Patients' self-reported difficulty in concentration or caregivers' observation of obvious inattention in daily life; (8)Intact visual field or normal visual field after correction; (9)Patients or their legal representatives voluntarily agree to participate in the study, comply with research procedures, and sign the informed consent form.
Exclusion criteria
Exclusion criteria: Exclusion Criteria (1)A prior history of neurological disease, brain injury, or psychiatric illness. (2)Severe complications, cardiopulmonary disease, uncontrolled hypertension, severe physical deformity, multiple organ damage or vital organ dysfunction, severe spasticity, etc. (3)Deterioration of condition, occurrence of new infarcts or hemorrhagic lesions; development of epilepsy or consciousness disturbance. (4)Drug abuse or chronic alcohol dependence. (5)Intracranial metal objects, intracranial tumors, intracranial infection, or any clinically significant/unstable medical disease. (6)Infection. (7)Contraindications for fNIRS measurement (e.g., skull defects or abnormalities). (8)Current use of medications that may affect cognitive function, such as antipsychotics or antidepressants. (9)Inability to cooperate with assessments or rehabilitation training. (10)Visual impairment and visual field defects; patients with hemispatial neglect. (11)Participation in other related research within the past 2 months.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| The span of attention was measured using the digit span test;Rapid Visual Digit Presentation Task;Stroop color-word test;Trail Making Test Part B;Paced Auditory Serial Addition Test;Montreal Cognitive Assessment;Activities of Daily Living;Detection of a Cognitive Rehabilitation Training System Based on Eye-Tracking Technology; | — |
Primary
| Measure | Time frame |
|---|---|
| Mini-Mental State Examination;Functional Near-Infrared Brain Imaging; | — |
Countries
China
Contacts
Public ContactJinqin Zhang
China Rehabilitation Research Center
Outcome results
None listed