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The Effects of tDCS Combined with Occupation-Based Cognitive Training on Post-Stroke Cognitive Impairment: An fNIRS Evaluation Study

The Effects of tDCS Combined with Occupation-Based Cognitive Training on Post-Stroke Cognitive Impairment: An fNIRS Evaluation Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113365
Enrollment
Unknown
Registered
2025-11-27
Start date
2025-12-05
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Stroke

Interventions

Control group:ADL-Based Cognitive Training
Experimental Group:tDCS combined with ADL-based cognitive training

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meets the stroke diagnostic criteria according to the "Chinese Guidelines for the Diagnosis and Treatment of Cerebral Hemorrhage (2019 edition)" and the "Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke (2018 edition)," and confirmed by CT or MRI, indicating the presence of cerebral infarction or cerebral hemorrhage; cognitive dysfunction is screened using the Montreal Cognitive Assessment (MoCA), with a total score <=25 indicating cognitive impairment; a MoCA score between 10-25 suggests mild to moderate cognitive impairment. 2. First-ever stroke, aged between 18-75 years; 3. Disease duration less than 6 months; 4. Education level of elementary school or above; 5. Patient’s condition is stable, conscious, and demonstrates good compliance; 6. Both the patient and family members are aware of the content of this study and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with a history of cerebral aneurysm or traumatic brain injury; 2. Individuals with a personal or immediate family history of epilepsy; 3. Neurodegenerative diseases; 4. Mental disorders; 5. Presence of metal foreign bodies in the head or implanted cranial/chest medical devices; 6. Individuals with severe depression, anxiety, or diagnosed with other mental illnesses that prevent cooperation in completing the experiment; 7. Individuals with impaired consciousness or speech function, making communication difficult.

Design outcomes

Secondary

MeasureTime frame
Activities of Daily Living (ADL);

Primary

MeasureTime frame
Cognitive Function;

Countries

China

Contacts

Public ContactYu Yin

Hebei General Hospital

yinyu-99@163.com+86 177 9809 3116

Outcome results

None listed

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