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Exploring the mechanism of action of transcranial direct current stimulation in the treatment of stroke-related cognitive impairment based on intracortical inhibition techniques

Exploring the mechanism of action of transcranial direct current stimulation in the treatment of stroke-related cognitive impairment based on intracortical inhibition techniques

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077453
Enrollment
Unknown
Registered
2023-11-09
Start date
2023-11-15
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Stroke related cognitive impairment

Interventions

True tDCS Stimulation Group:Stimulation Localization: The anode was placed above the left dorsolateral prefrontal cortex (DLPFC), while the cathode was placed near the right DLPFC .
Sham tDCS Stimulation Group:Sham transcranial direct current stimulation

Sponsors

Department of rehabilitation medicine, Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) It meets the diagnostic criteria of "stroke" [20], and all cases need to be confirmed as cerebral infarction or cerebral hemorrhage through clinical diagnosis and cranial CT or MRI examinations; (2) The patients' ages ranged from 30 to 75 years old, they experienced their first stroke within the past 1-6 months, their condition was stable, and their vital signs were stable; (3)Cognitive impairment occurs after a stroke, and the objective cognitive function assessment indicates the presence of cognitive impairment. However, the severity of cognitive impairment is not sufficient to prevent the patient from cooperating with the assessment and treatment (MoCA (Beijing version) total score of 10-26 points); (4) According to the Edinburgh Handedness scale (mean laterality score of 75%) [21], all subjects were right-handed; (5) Patients whose healthy side can measure the resting motor threshold; (6) The subjects themselves or their immediate family members signed the informed consent and voluntarily participated.

Exclusion criteria

Exclusion criteria: (1) The physical condition is unstable, and the function is reduced; (2) Have been pregnant or have a pregnancy plan in the next 3 months; (3) There are visual and hearing impairments or other factors affecting cognitive examination. (4) With a history of major mental disorders, diagnosed with dementia, autism spectrum disorder, or any other neurological disease except mild to moderate cognitive impairment, and diagnosed with bipolar disorder with manic or depressive episodes in the past year.; (5) They are currently in a state of moderate to severe depression or anxiety, with Hamilton Anxiety Scale (HAMA) = 14 points or Hamilton Depression Scale (HAMD) = 17 points; (6) Use of active drugs of the central nervous system or prescription or over-the-counter drugs (including benzodiazepines, anti-dementia drugs, cholinesterase inhibitors, etc.), abuse of any drugs (including nicotine and alcohol), or research drugs (baclofen and diazepam) ; (7) There are or have been serious adverse reactions to tDCS treatment; (8) TDCS contraindications (including epilepsy, tumor, VP shunt tube, metal implant, skull defect or crack, severe lung disease, multiple organ failure, etc.).;

Design outcomes

Primary

MeasureTime frame
Montreal Cognitive Assessment;

Secondary

MeasureTime frame
Mini-mental State Examination;modified Barthel index;interval intracortical inhibition;functional near-infra-red spectroscopy;

Countries

China

Contacts

Public ContactZhang Qun

Department of rehabilitation medicine, Huashan Hospital, Fudan University

zqun_888@163.com+86 156 1832 0648

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 29, 2026