Actively Recruiting

Age: 18Years - 50Years
All Genders
Healthy Volunteers
ID01617408

TMS Investigations of the Human Visual System

Led by National Institute of Mental Health (NIMH) · Updated on 2026-05-01

665

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how the brain processes visual information, focusing on two systems: one that recognizes what objects are and another that locates where objects are. The study aims to understand how these brain pathways contribute to recognizing different types of objects, using advanced brain imaging and stimulation techniques. This research involves healthy adults aged 18 to 50 who speak English. The study uses a series of experiments combining behavioral visual tasks with magnetic resonance imaging (MRI) and brain stimulation methods called transcranial magnetic stimulation (TMS) and transcranial electrical stimulation (tES). Participants may undergo fMRI scans to identify brain regions involved in vision before receiving either TMS or tES during or before performing visual recognition tasks. These tasks involve viewing images of faces, bodies, tools, and scenes, sometimes shown briefly, and responding via keyboard or button presses. The stimulation can enhance or disrupt brain activity to study its effect on task performance. Participants will attend multiple visits over up to three years, including screening exams and baseline brain scans. During visits, they will perform visual tasks alone or combined with brain imaging and stimulation. Researchers will measure task accuracy, reaction times, and brain activity changes related to the stimulation. Safety monitoring and detailed assessments will be conducted throughout the study to understand how brain pathways support visual recognition.

CONDITIONS

Brief Title

Brain Stimulation and Vision Testing

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy
  • Ages 18 to 50 years (inclusive)
  • Able to read and write in English to understand all study instructions
Not Eligible

You will not qualify if you...

  • Presence of ferromagnetic metal in the head or eyes, such as aneurysm clips or cochlear implants
  • Abnormal structural MRI findings
  • Implanted cardiac pacemaker or auto-defibrillator
  • Use of an insulin pump
  • Irremovable body piercings
  • Pregnancy
  • Visual impairments preventing task performance
  • Lack of consent capacity
  • Inability to understand study instructions
  • History of neurological problems including epilepsy, seizures, or recurrent migraines
  • Use of medications that lower seizure threshold
  • Significant psychiatric illness or history of psychiatric illness
  • Employees or family members of the National Institute of Mental Health (NIMH)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Single session

Participants undergo fMRI experiments to localize brain regions for targeted stimulation by viewing object categories or visual patterns.

1 visit (in-person)

Online Behavioral Stimulation Experiments

Duration - Varies per experiment

Participants perform visual behavioral tasks while receiving transcranial magnetic stimulation (TMS) or transcranial electrical stimulation (tES) to assess the direct effects of neural disruption or enhancement.

Multiple visits depending on task schedules

Offline Stimulation and Imaging Experiments

Duration - Sessions last up to 60 minutes of stimulation plus scanning time

Participants receive offline thetaburst stimulation (TBS) or tES prior to tasks and may undergo fMRI scanning before and after stimulation to measure neural and behavioral effects.

1 to 2 visits including fMRI sessions

Trial Site Locations

Total: 1 location

1

National Institutes of Health Clinical Center

Bethesda, Maryland, United States, 20892

Actively Recruiting

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Research Team

N

NIMH LBC Volunteer

C

Christopher I Baker, Ph.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Theta-burst TMS of lateral occipital cortex reduces BOLD responses across category-selective areas in ventral temporal cortex.

Iris I A Groen, Edward H Silson, David Pitcher...

https://pubmed.ncbi.nlm.nih.gov/33497776