A controlled study of computerized training for aphasia after stroke

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000033527

Enrollment

Unknown

Registered

2020-06-04

Start date

2020-06-10

Completion date

Unknown

Last updated

2020-06-08

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

Conditions

Aphasia after stroke

Interventions

1:traditional language training

2:traditional language training and computerized language training

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients with age 17, primary school level (education years 20, middle school or above (education years > 6) > 24); 7. Patients with consistent caregivers (> 3 days / week).

Exclusion criteria

Exclusion criteria: 1. Patients with other pathological brain diseases, such as vascular malformation, tumor, abscess, encephalitis or other common non ischemic brain diseases (such as multiple sclerosis), found on CT or MRI; 2. Patients with severe liver or kidney dysfunction (ALT value > 2 times the upper limit of normal value or ast value > 2 times the upper limit of normal value; creatinine > 1.5 times the upper limit of normal value); 3. Patients with severe heart failure; 4. Patients with confirmed or proposed acute coronary syndrome; 5. Patients with high-risk arrhythmias, such as: second or third degree atrioventricular block in sick sinus syndrome, tachycardia related syncope and atrial fibrillation caused by not installing pacemaker; 6. Other planned surgical operations or treatments may require termination of clinical observation; 7. Patients with severe non cardiovascular and cerebrovascular diseases whose expected survival time is less than 1 year; 8. Patients who are unable to understand and / or obey the research procedures and / or follow-up due to mental disorders and emotional disorders; 9. Patients with severe anxiety and depression (HAMD > 24, HAMA >= 29); 10. Patients with aphasia, blindness and deafness who are unable to complete neuropsychological assessment and other patients who are not considered suitable for the study.

Design outcomes

Primary

Measure	Time frame
Western Aphasia Battery;Aphasia Battery of Chinese;Video EEG plus flash stimulation;DTI;	—

Countries

China

Contacts

Public ContactChuanqiang Qu

Shandong Provincial Hospital

drquchuanqiang@sina.com+86 13583138679

Outcome results

None listed

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