Actively Recruiting

Phase Not Applicable
Age: 50Years - 85Years
All Genders
NCT07036328

Transcranial Magnetic Stimulation to Slow Down Cognitive Decline in Alzheimer's Disease

Led by Willem de Haan · Updated on 2026-05-12

55

Participants Needed

1

Research Sites

168 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

New amyloid-targeting drugs for Alzheimer's disease (AD) offer minimal or unclear efficacy and often cause adverse events, highlighting the need for new therapies. In recent years, repetitive transcranial magnetic stimulation (rTMS) has shown increasing success. A recent randomized, double-blind, sham-controlled, phase 2 demonstrated promising results from a 24-week rTMS treatment protocol targeting the precuneus. This brain region is considered a main hub of the human brain connectome and a prominent area of AD pathology. The results showed stable cognitive performance and increased brain activity in the treatment group, whereas the sham group worsened. A replication study is planned to further investigate the working mechanism of precuneus-rTMS in AD and to improve understanding of its therapeutic potential.

CONDITIONS

Official Title

Transcranial Magnetic Stimulation to Slow Down Cognitive Decline in Alzheimer's Disease

Who Can Participate

Age: 50Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Biomarker-supported Alzheimer's disease with abnormal CSF p-tau/Ab242 ratio above 0.023 or positive amyloid PET scan
  • Age between 50 and 85 years
  • Clinical Dementia Rating (CDR) score of 0.5 or 1
  • Mini-Mental State Examination (MMSE) score between 18 and 27
  • Presence of a caregiver
Not Eligible

You will not qualify if you...

  • History of neurodegenerative diseases other than Alzheimer's disease, stroke, or epilepsy
  • Severe psychiatric problems that interfere with study participation and may cause cognitive impairment, as assessed by an expert neurologist or psychiatrist
  • Extensive cerebrovascular damage on MRI classified as Fazekas level 2 or 3; patients with level 3 are excluded, and those with level 2 are evaluated by an expert neurologist
  • Presence of metal in the head or cranial/thoracic implants, including cochlear implants
  • Unstable dosing of cholinesterase inhibitors in the last 2 months
  • Extreme claustrophobia or metallic objects preventing MRI and MEG examinations
  • Previous treatment with repetitive transcranial magnetic stimulation (rTMS)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Amsterdam UMC

Amsterdam, Netherlands

Actively Recruiting

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Research Team

W

Willem De Haan, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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