Deep Repetitive Transcranial Magnetic Stimulation (rTMS) of the Precuneus for Alzheimer Disease (AD)

Recruiting now · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Alzheimer&Amp;Amp;#39;s Disease, Alzheimer Disease, Dementia Alzheimer Type, Mild Alzheimer&Amp;Amp;#39;s Disease, Moderate Alzheimer&Amp;Amp;#39;s Disease, Alzheimer&Amp;#39;s Disease (AD), Alzheimer&Amp;#39;s Dementia

In brief

The goal of this clinical trial is to learn if using deep repetitive transcranial magnetic stimulation (rTMS) targeting the precuneus is feasible, tolerable, and potentially efficacious for memory in Probable Alzheimer's Dementia. Previous work studying rTMS in Alzheimer's is mixed, but recent work studying rTMS of the precuneus is encouraging for both its short-term and long-term effects. The main questions this study aims to answer are: * Is deep rTMS of the precuneus feasible and tolerable in Alzheimer's? * Are there signs of positive brain changes in response to deep rTMS? * Is deep rTMS potentially efficacious for memory in Alzheimer's? Researchers will compare active stimulation to placebo stimulation while obtaining memory testing and measurements of the brain (imaging, scalp electrode measurements, bloodwork) to see if active treatment works to treat mild-to-moderate probable Alzheimer's Dementia. Participants will: * Engage with memory testing, brain scans, and bloodwork during a comprehensive assessment * Visit the clinic 3 times for 12 consolidated rTMS sessions, followed by 4 once weekly maintenance sessions * Be offered a full open-label active treatment course after completing their treatment course if they are initially in the placebo group

Key facts

Study ID: NCT06597942
Run by: University of California, Los Angeles
People needed: 54
Starts: 2024-10-17
Expected to finish: 2026-10-01
Last updated by the study team: 2026-01-21

Who can join

Age: 60 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Age 60-100 at the start of the study
Established diagnosis of Alzheimer's Clinical Syndrome (which is also met through a diagnosis of Alzheimer's Dementia)
Agreement to participate in study and able to complete informed consent process
Have a caregiver/study partner who can accompany them to all study visits
Have a known alternate surrogate decision-maker (in case needed) who can accompany them to the informed consent visit (this person may be the study partner mentioned above)
Screening MMSE score of 18-26
Screening GDS score \&lt;6
Either 1) treated with memory-enhancing medication (cholinesterase inhibitor) for at least 2 months, 2) failed trial with no plan to re-trial, or 3) no trial planned during the course of the study for other reasons
No change in use of psychotropic medication for the treatment of depression, anxiety, ADHD, or psychosis for 2 weeks prior to the study

You may not qualify if…

Participant and/or their surrogate are unwilling or unable to provide informed consent
Currently pregnant or potentially pregnant
Diagnosis of a dementia or cognitive disorder due to a cause other than Alzheimer's Disease
Diagnosis of severe Dementia (CDR \> 2.0) at the start of the study
History of substance use disorder currently not in sustained remission
Substance misuse within the past 6 months (excluding nicotine or caffeine)
History of stroke, traumatic brain injury with loss of consciousness, or other major neurologic disorder (e.g., epilepsy, Huntington's disease, Parkinson's disease)
History of seizure disorder or family history of seizure disorder in a first-degree relative
Poorly-controlled hypertension, cardiovascular disease, or cerebrovascular disease
History of any other major active medical, neurologic, or psychiatric illness affecting cognition (associated with cognitive impairment) or a participant's ability to safely and meaningfully participate in the study
Non-fluent in English (not native or functionally-native)
Contraindication to TMS or MRI including claustrophobia, MRI-incompatible or unknown metal in body (including facial tattoos with uknown or metallic inks), surgery within 60 days, certain implants (excluding dental fillings), or previous abnormal MRI results.
Has previous history of TMS treatment in the past (not TMS naïve)
Currently enrolled in a memory-enhancement study
Alteration in cognitive-enhancement medication dose within the past 2 months or active plans for dose alteration during the course of the study (previously unplanned changes that occur during the study will be examined on a case-by-case basis)
History of treatment with lecanemab, aducanumab, donanemab, or other monoclonal antibody treatment for Alzheimer's Disease (due to lack of knowledge surrounding the impacts of these treatments)
Currently or within the past 2 weeks taking any of the following classes of medication:
Anticholinergic (e.g., tolterodine, benztropine)
Sedating antihistamines (e.g., diphenhydramine)
any drug that has significant anticholinergic or antihistaminic side effects (e.g., tricyclic antidepressant medications, mirtazapine).
Benzodiazepines. While not a strict rule out, this will be decided on a case-by-case basis
Antiepileptic agents. While not a strict rule out, this will be decided on a case-by-case basis
Antipsychotic agents. While not a strict rule out, this will be decided on a case-by-case basis

Where it is running

UCLA TMS Clinical and Research Service — Los Angeles, California, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.