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Brain mechanism of multi-target high-frequency rTMS combined with pharmacological treatment to improve cognitive function in patients with AD

Brain mechanism of multi-target high-frequency rTMS combined with pharmacological treatment to improve cognitive function in patients with AD

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078341
Enrollment
Unknown
Registered
2023-12-05
Start date
2024-01-01
Completion date
Unknown
Last updated
2023-12-10

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

Conditions

Alzheimer

Interventions

Drug therapy group:The dose of Donepezil was increased to 10mg/d for 12 weeks. If the patient has insomnia, change to morning medication
Combined treatment group A:High frequency rTMS true stimulus (stimulus parameters are as follows: the stimulus frequency is 20Hz
The stimulation duration was 2s and the interval was 28s. Each target stimulated 15 sequences with 600 pulses, a total of 60 sequences with 2400 pulses, a total treatment time of 30 minutes) +5mg/d Do
Combined treatment group B:High frequency rTMS sham stimulus +5mg/d Donepezil

Sponsors

Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 89 Years

Inclusion criteria

Inclusion criteria: ? Meet the Diagnostic and Statistical Manual of Mental Disorders Revised IV and the Working Group standards of the National Academy of Neurology, Speech and Communication Disorders, and Stroke-Alzheimer's Disease and Related Disorders; ? All patients were Han and right-handed; ? Education level of 8 years or above; (4) Complete all clinical and cognitive behavioral scales required by the experiment; (5) Move freely without the help of others; ? No history of alcohol consumption or drug dependence; ? No epilepsy and family history; No MRI contraindications, such as claustrophobia and metal implants.

Exclusion criteria

Exclusion criteria: ? Have a history of severe trauma or mental illness; ? Patients with severe ischemic lesions; ? Patients with depression and/or anxiety; ? patients with arteriosclerosis or leukoporosis; ? Overweight, Body Mass Index (BMI) = 28.

Design outcomes

Secondary

MeasureTime frame
structural magnetic resonance imaging,sMRI;diffusion tensor imaging,DTI;

Primary

MeasureTime frame
Cognitive behavioral assessment;

Countries

China

Contacts

Public ContactDong Cui

Shandong First Medical University

cuidong_cd@126.com+86 13053806128

Outcome results

None listed

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