Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT06050603

MRI Guided Closed-loop TMS-EEG

Led by Sunnybrook Health Sciences Centre · Updated on 2024-08-13

160

Participants Needed

1

Research Sites

203 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this interventional study is to develop an individualized approach using transcranial magnetic stimulation (TMS) in a high-precision manner. This approach will use TMS to modulate brain activity at multiple locations simultaneously. Functional magnetic resonance imaging (fMRI) and electroencephalograph (EEG) will record the responses and guide the stimulation. Specifically, the placement and orientation of TMS coils will be tailored to stimulate the targeted functional brain areas informed by fMRI. To maximize the interventional effect, stimulation pulses will be delivered based on EEG oscillations.

CONDITIONS

Official Title

MRI Guided Closed-loop TMS-EEG

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • For healthy participants: aged 18 to 65 years
  • Healthy with no history of neurological impairment
  • Normal or corrected-to-normal vision
  • For participants with amnestic mild cognitive impairment (aMCI): aged 50 to 80 years
  • Cognitive symptoms including a self- or informant-reported complaint, preserved independence, and no dementia
  • Objective cognitive impairment shown by Mini-Mental State Exam score 24-27, Montreal Cognitive Assessment score 18-26, or Clinical Dementia Rating Scale score of 0.5
  • Normal or corrected-to-normal vision
Not Eligible

You will not qualify if you...

  • Women who are pregnant or breastfeeding
  • History of seizures (except childhood febrile seizures), epilepsy in self or first-degree relatives, stroke, brain tumor, brain surgery, head injury, or known brain lesions
  • Presence of metal in the eye or skull area, brain stimulators, surgical metal, clips in the brain, cochlear implants, or metal fragments in the eye
  • Non-MRI compatible metal implants such as cardiac pacemakers or aneurysm clips
  • Claustrophobia or inability to lie comfortably supine for up to 1 hour
  • Participation in any other non-invasive brain stimulation study within the last two weeks
  • Abnormal neurological examination findings

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

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada, M4N 3M5

Actively Recruiting

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Research Team

F

Fa-Hsuan Lin, PhD

CONTACT

H

Hsin-Ju Lee, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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