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Multicenter, Randomized, Controlled Clinical Trial of Cerebellar Intermittent Theta Burst Stimulation (iTBS) Transcranial Magnetic Stimulation for the Treatment of Mild-to-Moderate Alzheimer's Disease

Multicenter, Randomized, Controlled Clinical Trial of Cerebellar Intermittent Theta Burst Stimulation (iTBS) Transcranial Magnetic Stimulation for the Treatment of Mild-to-Moderate Alzheimer's Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127932
Enrollment
Unknown
Registered
2026-07-10
Start date
2026-07-10
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Alzheimer‘s disease

Interventions

Experimental group:Cerebellar intermittent theta burst stimulation (iTBS)
Control group: Sham stimulation

Sponsors

The First Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 50–80 years old; 2. MMSE score between 18–26, Clinical Dementia Rating (CDR) score of 0.5–1; Hamilton Depression Rating Scale (HAM-D) score =14; 3. Meet the NIA-AA criteria established by the U.S. National Institute on Aging; cerebrospinal fluid shows increased Aß and decreased tau protein. 4. Have been on a stable dose of a cholinesterase inhibitor (such as donepezil or galantamine) for at least 6 weeks, with no dose changes needed during the intervention and observation period; 5. Able to cooperate with treatment and related examinations; 6. Patient and family voluntarily sign the informed consent form

Exclusion criteria

Exclusion criteria: 1. Unable to cooperate to complete treatment and various tests 2. Having serious infections, epilepsy, cerebrovascular diseases, malignant tumors, or serious heart, liver, kidney dysfunction, mental disorders, alcoholism, drug dependence, or psychiatric illnesses 3. Having contraindications for transcranial magnetic stimulation and MRI, such as metal or implanted devices in the body, like pacemakers or deep brain stimulators 4. Participating in another clinical trial at the same time 5. Patient or family withdraws informed consent.

Design outcomes

Primary

MeasureTime frame
Change from Baseline in Clinical Dementia Rating Scale Sum of Boxes (CDR-SB);

Secondary

MeasureTime frame
Change from Baseline in Delayed Matching-to-Sample (DMS) task performance and simultaneous electroencephalography (EEG) features;Change from Baseline in Mini-Mental State Examination (MMSE) score;Change from Baseline in Alzheimer‘s Disease Assessment Scale-Cognitive Subscale (ADAS-Cog) score;Change from Baseline in Activities of Daily Living (ADL) scale score;Change from Baseline in Neuropsychiatric Inventory (NPI) total score;Changes on magnetic resonance imaging (MRI) before and after treatment;

Countries

China

Contacts

Public ContactWen Jiang

The First Affiliated Hospital of Air Force Medical University

jiangwen@fmmu.edu.cn+86 173 9298 5036

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026