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To explore the mechanism of computerized cognitive remediation therapy on post-stroke cognitive recovery

To explore the mechanism of computerized cognitive remediation therapy on post-stroke cognitive recovery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102047
Enrollment
Unknown
Registered
2025-05-07
Start date
2022-07-08
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Post Stroke Cognitive Impairment patients

Interventions

Experimental group:computerized cognitive remediation therapy
Control group:cognitive tasks of occupational therapy

Sponsors

Beijing Bo'ai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of stroke adopted by the Fourth National Conference on Cerebrovascular Diseases, and the diagnosis is confirmed by CT or MRI; 2. First onset, course of disease 2 weeks to 6 months; 3. The age of 20-80 years old, education level of primary school or above; 4. Clear mind, stable condition, certain oral expression and understanding ability, can cooperate with the completion of Loewenston Occupational Therapy Cognitive Assessment; 5. There are clear cognitive dysfunction: the MMSE scores of primary school education (schooling years 1-6 years) =20 points, middle school education (schooling years 6-12 years) =24 points, high school above (schooling years >12 years) score <27 points; 6. At least one limb can complete simple computer operations; 7. can keep sitting for 30 minutes;

Exclusion criteria

Exclusion criteria: 1. with other mental diseases and severe nervous system diseases; 2. Cognitive impairment before stroke or due to other causes; 3. Complicated with other serious heart, lung, renal insufficiency, serious liver function and malignant tumor; 4. Severe visual, hearing and language impairment, which interferes with cognitive assessments; 5. can not cooperate with assessment and rehabilitation training; 6. Patients or their family members refuse to sign informed consent;

Design outcomes

Primary

MeasureTime frame
Score of MMSE;Score of LOTCA;Modified Barthel Index;Score of rBANS;

Countries

China

Contacts

Public ContactRuxiu Yan

Beijing Bo'ai Hospital

18001355750@126.com+86 10 87569536

Outcome results

None listed

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