Modulating Reward Learning Using Transcranial Magnetic Stimulation

Description

Our specific aim is to examine the effects of TMS on reward processing during goal-directed behavior. In these experiments the investigators will utilize a scalp-recorded brain oscillation called frontal midline theta that is believed to index the sensitivity of the cingulate cortex to reward feedback. Here the investigators will asked whether this electrophysiological signal can be modulated up or down using TMS while participants engage in decision making tasks, and if so, whether it would affect the encoding of rewards and subsequent choices during task performance.

Conditions

Behavior

Study Overview

Study Details

Study overview

Our specific aim is to examine the effects of TMS on reward processing during goal-directed behavior. In these experiments the investigators will utilize a scalp-recorded brain oscillation called frontal midline theta that is believed to index the sensitivity of the cingulate cortex to reward feedback. Here the investigators will asked whether this electrophysiological signal can be modulated up or down using TMS while participants engage in decision making tasks, and if so, whether it would affect the encoding of rewards and subsequent choices during task performance.

Modulating Reward Learning Using Transcranial Magnetic Stimulation

Modulating Reward Learning Using Transcranial Magnetic Stimulation

Condition
Behavior
Intervention / Treatment

-

Contacts and Locations

Newark

Rutgers University - Newark, Newark, New Jersey, United States, 07102

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Be between the ages of 18 and 55 years old.
  • * Be in stable mental and physical health.
  • * If female, test non-pregnant.
  • * Be willing to provide informed consent.
  • * Be able to comply with protocol requirements and likely to complete all study procedures.
  • * Contraindication to rTMS (history of neurological disorder or seizure, increased intracranial pressure, brain surgery, or head trauma with loss of consciousness for \> 15 minutes, implanted electronic device, metal in the head, or pregnancy).
  • * History of autoimmune, endocrine, viral, or vascular disorder affecting the brain.
  • * Life time history of mental disorders such as: Bipolar Affective disorder (BPAD), Schizophrenia, Post-traumatic Stress disorder (PTSD) or Dementia or Major Depression.
  • * uninterruptable central nervous system medication

Ages Eligible for Study

18 Years to 55 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Rutgers, The State University of New Jersey,

Study Record Dates

2025-04-30