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Study of the Effect of Transcutaneous Auricular Vagus Nerve Stimulation-Cognitive Rehabilitation Training Synchronized Collaborative Model on Post-Stroke Cognitive Impairment

Study of the Effect of Transcutaneous Auricular Vagus Nerve Stimulation-Cognitive Rehabilitation Training Synchronized Collaborative Model on Post-Stroke Cognitive Impairment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000055
Enrollment
Unknown
Registered
2026-01-13
Start date
2025-12-01
Completion date
Unknown
Last updated
2026-02-02

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

Routine Cognitive Rehabilitation Therapy Group:Cognitive training is conducted for individuals with varying degrees of cognitive impairment, targeting specific cognitive domains such as attention, mem
taVNS-train Synchronized Therapy Group:Concurrent with routine rehabilitation training, taVNS intervention is implemented. Based on the patients degree of cognitive impairment, targeted methods are se

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: The diagnostic criteria are based on the 2017 Expert Consensus on the Management of Post-stroke Cognitive Impairment and the "Chinese Guidelines for the Prevention and Treatment of Cerebrovascular Diseases (2021 Edition)": 1. Patients diagnosed with cerebral infarction via MRI or CT, or intracerebral hemorrhage, or lacunar infarction; 2. Presence of PSCI (diagnostic criteria refer to the 2017 Expert Consensus on the Management of Post-stroke Cognitive Impairment), with MMSE scores =17 for illiterate individuals, =20 for primary school graduates, and =24 for those with middle school education or above; or MoCA scores <26; 3. Age between 20 and 85 years; 4. Right-handed; 5. Educational level of primary school or above; 6. Last episode within 24 months; 7. Voluntarily participating in this research project and signing the informed consent form.

Exclusion criteria

Exclusion criteria: a. Mood or mental disorders, visual and auditory impairments, severe heart, liver, or kidney diseases, or infectious diseases, Parkinson's disease, epilepsy, or a first-degree relative with a history of idiopathic epilepsy, and those using epileptogenic drugs; b. Skull defects, individuals with pacemakers, or those with metal implants in the body who are unsuitable for MRI; c. Those with pre-existing damage to the musculoskeletal system.

Design outcomes

Primary

MeasureTime frame
Mini-mental State Examination;

Secondary

MeasureTime frame
Montreal Cognitive Assessment Scale;MRI Data;

Countries

China

Contacts

Public ContactZhao Jingjun

Peking University People's Hospital?

tongchengzjj@163.com18813081710

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026