Stroke
Conditions
Interventions
Bidirectional visual interaction:The task progress is completely driven by the visual intentions of the subjects
One-way visual feedback:The system automatically presented the target, and the subject actively moved to the target, which was an active rehabilitation mode
Static visual presentation:The task began by presenting static targets that subjects completed passively, representing traditional passive training
Confusion of visual intention:Subjects chose the target with gaze, but the system randomly triggered another target to test whether motor improvement was indeed the result of alignment of intention wi
Sponsors
The First Affiliated Hospital of Naval Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.40-70 years old, gender not limited, right-handed; 2.No upper limb motor dysfunction, active range of motion (elbow) was >= 80% of the normal range; 3.The ability to perform autonomous eye movements is basically normal. Visual acuity or corrected visual acuity >=0.8, no color blindness, color weakness or other serious ophthalmic diseases; 4.No neurological diseases such as stroke or Parkinson's disease, or severe cognitive impairment, and capable of understanding and cooperating in the execution of task instructions; 5.The subjects fully understood the treatment plan, signed the consent form, and took the initiative to cooperate with the plan and voluntarily participated in this study.
Exclusion criteria
Exclusion criteria: 1.There are severe functional disorders or organic diseases of the heart, lungs, liver, kidneys, etc; 2.Recent (within 3 months) history of head trauma, infection, or surgery; 3.Severe visual and hearing impairment, impairing cognitive assessment; 4.Inability to cooperate with eye-tracking or upper-limb training tasks (e.g., visual and hearing impairment, cognitive impairment, motion sickness, etc.); 5.Subjects who do not consent to the study or are unable to cooperate with the treatment regimen; 6.Is participating in another clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in Hemoglobin Content (?HbO2);Sports data;Eye movement data; | — |
Secondary
| Measure | Time frame |
|---|---|
| Activation duration;Activate synergy; | — |
Countries
China
Contacts
Public ContactFang Fanfu
The First Affiliated Hospital of Naval Medical University
Outcome results
None listed