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Development and Multicenter Validation of a Personalized Transcranial Alternating Current Stimulation Protocol for Cognitive Impairment in Older Adults

Development and Multicenter Validation of a Personalized Transcranial Alternating Current Stimulation Protocol for Cognitive Impairment in Older Adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117984
Enrollment
Unknown
Registered
2026-01-30
Start date
2025-09-19
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

Alzheimers disease

Interventions

Gamma Transcranial Alternating Current Stimulation (tACS) Group:Transcranial Alternating Current Stimulation (tACS)

Sponsors

Xuanwu Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Inpatients or outpatients aged 50–90 years; 2.Patients diagnosed with amnestic mild cognitive impairment (aMCI) due to AD or mild dementia due to AD, based on the 2018 NIA-AA clinical diagnostic criteria established by the National Institute on Aging and the Alzheimer’s Association; 3.Neuropsychological assessment showing MMSE scores between 18 and 26, and a CDR score of 0.5 or 1; 4.Able to communicate fluently in Chinese (non-illiterate); 5.For those currently receiving cholinesterase inhibitor therapy (e.g., donepezil or rivastigmine), the treatment dose must be stable, defined as a fixed dosage administered continuously for at least six weeks, with no adjustment of the medication regimen during the study period; 6.Provision of written informed consent. 7. Positive amyloid PET, or decreased amyloid levels in cerebrospinal fluid, or elevated serum phosphorylated Tau217 protein.

Exclusion criteria

Exclusion criteria: 1. Sudden onset of illness; 2. Early focal neurological symptoms or extrapyramidal symptoms; 3. Presence of systemic diseases that may lead to cognitive impairment (such as liver or kidney dysfunction, endocrine disorders, and vitamin deficiencies), or neurological diseases such as brain trauma, epilepsy, encephalitis, and normal pressure hydrocephalus; 4. Meets DSM-IV criteria for depression and schizophrenia; 5. Ongoing medication that may affect baseline and follow-up study periods; 6. Patients with contraindications to MRI and neurophysiological examinations, such as those with cardiac pacemakers, defibrillators, implanted electronic systems, vascular clips, mechanical heart valves, or cochlear implants; 7. Cranial MRI showing ischemic lesions consistent with NINCDS-AIREN criteria.

Design outcomes

Primary

MeasureTime frame
Moca score;

Countries

China

Contacts

Public ContactYueyi Yu

Xuanwu Hospital, Capital Medical University

yuyueyi@xwhosp.org+86 10 8319 8193

Outcome results

None listed

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