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Clinical research on the effect of cognitve assessments and training all-in-one machine to post-stroke cognitve impairment

Clinical research on the effect of cognitve assessments and training all-in-one machine

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034027
Enrollment
Unknown
Registered
2020-06-21
Start date
2020-07-04
Completion date
Unknown
Last updated
2020-07-20

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

Interventional Group:computerized cognitve training+conventional rehabitation training
Control group:computerized cognitve training in the same difficulty level+conventional rehabitation training

Sponsors

Affiliated Rehabilitation Hospital of Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria of stroke and are confirmed by CT or MRI; 2. For the first stroke patients, the course of disease is within 1 year, and the patients whose course of disease is less than or equal to 3 months should be included first, with clear consciousness and stable vital signs; 3. The patients who complain about their memory or cognitive function decline, or have cognitive dysfunction after confirmation, the score of MOCA scale is less than 25 points, the cognitive impairment occurs after stroke, and the cognitive impairment caused by other reasons is excluded; 4. Patients aged 40-80 years; 5. Patients with education level at or above primary school; 6. Patients who can complete simple computer operation on at least one limb; 7. Patients who can keep sitting position for 30 minutes; 8. Patients who voluntarily participate in the research project (those who are willing to sign the informed consent) can understand, receive rehabilitation guidance and implement it, and their families can assist in rehabilitation exercise.

Exclusion criteria

Exclusion criteria: 1. Patients with hypertension and uncontrolled blood pressure (systolic blood pressure (HP) is greater than 160mmhg or diastolic blood pressure (LP) is greater than 100mmhg); 2. Neurologists exclude patients with dementia and mental diseases according to the diagnostic criteria of the 10th edition of the international classification of diseases (ICD-10) of the World Health Organization and the fourth edition of the diagnostic and Statistical Manual of mental diseases (DSM-IV) of the American Psychiatric Association; 3. Patients with mental disorder, serious heart disease, malignant tumor, liver, renal failure, gastrointestinal bleeding, etc; 4. Patients with history of alcohol and drug abuse have taken drugs that affect cognitive function; 5. Patients with Hamilton Depression Scale score > 10; 6. Patients with visual / auditory impairment or writing / reading impairment affecting training and evaluation; 7. Patients who are participating in clinical trials of other subjects.

Design outcomes

Primary

MeasureTime frame
Montreal Cognitve Assessment;Alzheimer's Disease Assessment Scale-cognitive subscale;

Secondary

MeasureTime frame
Oxford Cognitive Screening Scale (Putonghua);Shape Trail Test-B;Modified Barthel Index;Instrumental Activities of Daily Living scale;

Countries

China

Contacts

Public ContactCai Sufang

Affiliated Rehabilitation Hospital of Fujian University of Traditional Chinese Medicine

178870666@qq.com+86 158599019854

Outcome results

None listed

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