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Modulation of Cognitive Control Signals in Prefrontal Cortex by Rhythmic Transcranial Magnetic Stimulation

Sponsored by University of North Carolina, Chapel Hill

About this trial

Last updated 5 years ago

Study ID

18-1789

Status

Completed

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18-75 Years
18 to 35 Years
All
All

Trial Timing

Ended 6 years ago

What is this trial about?

Purpose: In this study, the investigators will provide causal evidence for the role of alpha and theta oscillations in cognitive control. Participants: Participants must be healthy, between the ages of 18 and 35, right handed, able to provide informed consent, willing to comply with all study procedures, and be available for the duration of the study, speak and understand English. Procedures: Alpha and theta brain oscillations will be measured and then entrained using frequency specific rhythmic TMS during a retrospective cued cognitive control task.

What are the participation requirements?

Yes

Inclusion Criteria

- Healthy

- Between the ages of 18 and 35

- Right handed

- Able to provide informed consent

- Willing to comply with all study procedures

- Available for the duration of the study

- Speak and understand English.

No

Exclusion Criteria

- Attention Deficit Hyperactivity Disorder (currently under treatment)

- Neurological disorders and conditions, including, but not limited to: History of epilepsy Seizures (except childhood febrile seizures) -Dementia

- History of stroke

- Parkinson's disease

- Multiple sclerosis

- Cerebral aneurysm

- Brain tumors

- Medical or neurological illness or treatment for a medical disorder that could interfere with study participation (e.g., unstable cardiac disease, HIV/AIDS, malignancy, liver or renal impairment)

- Prior brain surgery -Any brain devices/implants, including cochlear implants and aneurysm clips -Cardiac pacemaker -Any other implanted electronic device -History of current traumatic brain injury -(For females) Pregnancy or breast feeding -Anything that, in the opinion of the investigator, would place the participant at increased risk or preclude the participant's full compliance with or completion of the study