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Efficacy and Mechanisms of Neuromodulation-Enhanced Cognitive Training Strategy in Patients with Amnestic Mild Cognitive Impairment

Efficacy and Mechanisms of Neuromodulation-Enhanced Cognitive Training Strategy in Patients with Amnestic Mild Cognitive Impairment

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112732
Enrollment
Unknown
Registered
2025-11-19
Start date
2025-11-27
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

amnestic mild cognitive impairment

Interventions

treatment group: paired-associative stimulation combined with cognitive training
control group:single-target stimulation combined with cognitive training

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. meet the diagnostic criteria for amnestic mild cognitive impairment (aMCI) and have never taken cognitive improvement medication; 2. be >=50 and <=80 years of age, of either sex, and right-handed; 3. complaints of memory loss with objective evidence (long-delayed recall scores on the Auditory Word Learning Test are at least 1.0 standard deviation below the mean of the age-matched population); 4. have a primary school education or higher; 5. understand, agree to participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Concurrent tumours, severe cardiac, hepatic, renal, or haematological disorders, or infectious diseases; 2. History of cerebrovascular disease, Parkinson's syndrome, or dementia of any aetiology; 3. History of anxiety, depression, schizophrenia, or other psychiatric disorders; 4. Severe visual or auditory impairment; 5. Presence of MRI contraindications (e.g., cardiac pacemakers, cardiac stents, artificial heart valves, surgical fixation plates following fracture surgery).

Design outcomes

Primary

MeasureTime frame
Auditory Verbal Learning Test Fifth Trial ;

Secondary

MeasureTime frame
Neuropsychological evaluations;Magnetic Resonance Imaging;

Countries

China

Contacts

Public ContactLu Juan-Juan

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese

1577510729@qq.com+86 176 2183 2760

Outcome results

None listed

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