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NCT06669182Recruiting

Advantage of Cerebellar Transcranial Magnetic Stimulation in Alzheimer's Diseases (ACT-AD)

Effects of Cerebellar Transcranial Magnetic Stimulation on Patients With Alzheimer's Disease:A Multicenter Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 24 Nov 2025

Brief summary (registry, in English)

Alzheimer's Disease (AD) is the primary cause of dementia, with its prominent feature being cognitive decline. The cerebellum plays a crucial role in cognitive processing, making it a potential target for therapeutic intervention. This study will be conducted to evaluate the efficacy and safety of cerebellar Intermittent theta-burst stimulation (CRB-iTBS) in participants with mild Alzheimer's disease on the change from baseline in the Clinical Dementia Rating-Sum of Boxes (CDR-SB) at 3 months of treatment in the Core Study. This project aims to provide a valid treatment to improve the cognitive function and quality of life for those with Alzheimer's disease.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
31 Oct 2024
Start date
7 Jan 2025
Primary completion date
10 Mar 2026
Lead sponsor
Xijing Hospital
NCT number
NCT06669182

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 7 Jan 2025 to the primary completion date, 10 Mar 2026
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participate in AD related clinical trials within 6 months prior to research registration

Other illness

  • Neurodegenerative disorders other than AD.
  • History of seizure (with the exception of febrile seizures in childhood)
  • Any of the following psychotic disorders (DSM IV-TR criteria):
    • Major depressive disorder (current)
    • Schizophrenia
    • Other psychotic disorders, bipolar disorder, or substance related disorders (within the past 5 years)
  • Cerebrovascular disease, severe infection, malignant tumor, or severe dysfunction of organs such as heart, liver, and kidney.

Other

  • Significant intracranial focal or vascular pathology seen on brain MRI scan
  • GDS score ≥ 8 points in baseline assessment
  • Pregnant or lactating women
  • Contraindications for TMS or MRI, metal or implanted devices in the body (such as pacemakers, deep brain stimulators).

Who the study is looking for

  • Age: 50-85 years old
  • Meet the core clinical criteria of NIA-AA for possible Alzheimer's disease dementia, and PET or cerebrospinal fluid markers show elevated p-tau and decreased A β (1-42)
  • MMSE score ranges from 18-26 points; CDR score 0.5-1 points
  • The patient has received treatment with acetylcholinesterase inhibitors (AChEI), NMDA receptor antagonists, or mannequine therapy, and the current dosing regimen has remained stable for the 12 weeks prior to baseline assessment
  • At least one adult caregiver
  • The patient or legal guardian voluntarily signs the informed consent form

Age in the registry: 50 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tangdu Hospital of Air Force Military Medical University
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Xi'anChinaRecruiting
Xijing Hospital of Air Force Military Medical University
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Xi'anChinaRecruiting
The First Affiliated Hospital of Xi'an Medical University
Coordinator of this site? Confirm its status
Xi'anChinaRecruiting
The Third Hospital of Xi'an
Coordinator of this site? Confirm its status
Xi'anChinaRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.