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Effects of self-regulated learning and computer-assisted cognitive training on cognitive function and activities of daily living in patients with cognitive dysfunction after stroke

Effects of self-regulated learning and computer-assisted cognitive training on cognitive function and activities of daily living in patients with cognitive dysfunction after stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013042
Enrollment
Unknown
Registered
2017-10-19
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-10-23

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

Conditions

Post-stroke Cognitive Impairment

Interventions

Self-regulated learning group:computer-assisted cognitive training and basic activities of daily living training and self-regulated learning
Demonstration study group:computer-assisted cognitive training and basic activities of daily living training and demonstration study
Traditional training group:Traditional cognitive training and basic activities of daily living training and demonstration study

Sponsors

Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Diagnostic criteria for stroke in the 2010 guidelines for the prevention and treatment of cerebrovascular diseases in China,and confirmed by computed tomography or magnetic resonance imaging; 2. First ever stroke and within one year poststroke; 3. Aged between 45 and 80 years old, education level is primary school or above; 4. Cognitive impairment was identified by the Fuzhou version of the Montreal cognitive assessment scale, and the score is between 10 and 26 points; 5. Cognitive impairment occurs after stroke and excludes other causes; 6. The patient is conscious and the vital signs are stable; 7. Can simply perform computer operations; 8. The patients self or their legal guardian have informed consent and have signed the informed consent

Exclusion criteria

Exclusion criteria: 1. Patients who have serious visual or hearing impairment, mental disorders that effect Cognitive examination; 2. Patients who have severe unilateral spatial neglect; 3. Prior to the onset of obvious mental decline, dementia; 4. The Hamilton depression scale scored >7 points and had depressive symptoms; 5. Combined with serious heart disease, liver, renal failure, malignant tumors, gastrointestinal bleeding and other diseases; 6. Patients who are included in other clinical trials that would affect the evaluation results of this study.

Design outcomes

Primary

MeasureTime frame
Cognitive function;activity of daily living;Daily life manipulation;

Secondary

MeasureTime frame
attention;memory;execution;

Countries

China

Contacts

Public ContactJing Tao

Fujian University of Traditional Chinese Medicine

taojing01@163.com+86 13305029119

Outcome results

None listed

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