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The impact of intelligent device assisted cognitive training on cognitive impairment and psychological status after stroke: a randomized clinical study

The impact of intelligent device assisted cognitive training on cognitive impairment and psychological status after stroke: a randomized clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128070
Enrollment
Unknown
Registered
2026-07-14
Start date
2026-07-17
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Stroke

Interventions

Control group:The control group received routine cognitive function training and increased the intensity of attention and memory training. Treat for 5 days a week, once a day for 30 minutes each time,
experimental group:Adding smart devices to the control group to help with treatment.

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. All patients were diagnosed with cerebral hemorrhage or stroke; the course of the disease lasts from 10 days to 24 months; 2. Evidence of moderate to severe cognitive impairment (i.e., MMSE score <= 19 points); 3. No history of mental illness (such as delirium, mania, or other mental illnesses); 4. Good treatment compliance, able to cooperate with treatment for at least 30 minutes; 5. Age between 18 and 60 years old; 6. All patients have stable vital signs and clear consciousness; 7. Education level of primary school or above.

Exclusion criteria

Exclusion criteria: 1. The patient's condition is complex, with unstable vital signs or active epilepsy; 2. There are obvious visual or hearing impairments that prevent the use of computers; 3. Serious underlying diseases with functional failure of other organs, such as malignant tumors, liver and kidney failure, etc.; 4. Unable to understand simple verbal instructions; 5. Significant mental symptoms or serious behavioral changes; 6. The patient is physically weak and unable to cooperate with half an hour of treatment.

Design outcomes

Primary

MeasureTime frame
Cognitive function;

Countries

China

Contacts

Public ContactSun dengjuan

Lanzhou University Second Hospital

sundengjuancom@163.com+86 1815200135

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026