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To explore the effect of cognitive rehabilitation training system based on eye tracking technology on unilateral neglect in stroke patients

To explore the effect of cognitive rehabilitation training system based on eye tracking technology on unilateral neglect in stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075767
Enrollment
Unknown
Registered
2023-09-14
Start date
2023-10-09
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

cerebral stroke

Interventions

Patient control group:Routine occupational therapy ?Routine unilateral neglect therapy
Patient intervention group:Routine occupational therapy ?Routine unilateral neglect therapy?Eye tracking technology cognitive therapy

Sponsors

China Rehabilitation Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) All patients meeting the diagnostic criteria; (2) in the subacute stage of stroke (1-6 months after onset); (3) No sensory aphasia and understanding disorders, the right hand can hold a pen; (4) The Mini mental State Examination (MMSE) score is greater than or equal to 10, or it can cooperate with rehabilitation treatment; (5) Right-handed, age 18-65 years old, junior high school or above; (6) The visual field is complete or normal after correction; (7) The patient's condition was stable and he was able to complete the test in a seated position; (8) The patient is willing to actively cooperate with the doctor's treatment and voluntarily sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with other psychiatric diseases, neurological diseases: such as disability, agnosia, visual impairment and visual field loss :(2) deterioration of the condition, new infarction, bleeding lesions :(3) epilepsy or consciousness disorders; (4) Recent use of tricyclic antidepressants, sedatives or various therapeutic pumps; (5) Pregnant women and children :(6) visual impairment and visual field loss; (7) can not cooperate with examination and rehabilitation training; (8) The patient or his family member refuses to sign the informed consent;

Design outcomes

Primary

MeasureTime frame
Line cancellation test;Star cancellation test;Straight-line bisection test;Letter cancellation test;Graphic copying test;Catherine Bergego Scale;Cognitive rehabilitation training system test based on eye tracking technology;—

Secondary

MeasureTime frame
Apple cancellation test;Modified Barthel Index;—

Countries

China

Contacts

Public ContactWenshuai Wang

China Rehabilitation Research Center

693035831@qq.com+86 152 6759 9465

Outcome results

None listed

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