Status:

RECRUITING

TMS for Cognitive Decline in Aging and Preclinical AD

Lead Sponsor:

Massachusetts General Hospital

Conditions:

Prodromal Alzheimer's Disease

Preclinical Alzheimer's Disease

Eligibility:

All Genders

40-99 years

Phase:

NA

Brief Summary

In this research study we want to learn more about the effects of non-invasive brain stimulation on motivation, memory, and brain-network function in cognitively unimpaired older adults and individual...

Eligibility Criteria

Inclusion

  • Between the ages of 40-99
  • Native English speakers
  • Willing and able to consent to the protocol and undergo imaging and neuropsychological testing at the specified time points
  • Cognitively normal older adults and individuals with preclinical Alzheimer's disease will be included.

Exclusion

  • History of head trauma involving loss of consciousness or alteration in consciousness
  • Another major neurologic or psychiatric condition
  • Known presence of a structural brain lesion (e.g. tumor, cortical infarct)
  • Any contraindication to MRI, such as presence of pacemakers, aneurysm clips, artificial heart valves, ear implants, metal fragments, or foreign objects in the eyes, skin, or body
  • Longstanding premorbid history (i.e. longer than 10 years) of alcohol or substance abuse with continuous abuse up to and including the time that the symptoms leading to clinical presentation developed
  • Any significant systemic illness or unstable medical condition which could lead to difficulty complying with the study protocol.
  • Unwilling to return for follow-up, undergo neuropsychological testing, TMS, and MR imaging
  • History of unprovoked seizures (i.e., seizures that occur in the absence of a clear provocation such as hyponatremia, hypoglycemia, etc.).
  • Subjects who have a first degree relative (e.g., father, mother or sibling) with a seizure disorder.
  • Subjects currently taking, or plan to take, medications which are highly epileptogenic. These include: clozapine, high doses of bupropion (i.e., greater than 400mg daily), diphenhydramine, cyclosporine, isoniazid, imipenem, chloroquine, tramadol and theophylline.

Key Trial Info

Start Date :

April 7 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

August 31 2029

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT06956300

Start Date

April 7 2025

End Date

August 31 2029

Last Update

July 14 2025

Active Locations (1)

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1

Massachusetts General Hospital

Boston, Massachusetts, United States, 02129