Identify the Optimal TMS Pulse Protocol to Modulate Reward Activity

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-55
SponsorRutgers, The State University of New Jersey

About this trial

The primary goal will be to identify the optimal pulse protocol by systematically measuring the efficacy of various theta burst stimulation and repetitive rTMS protocols to increase and decrease the reward positivity in dependent smokers. The secondary objective will be to measure the protocols' effectiveness to increase decision-making capacity using the probabilistic selection task (PST). The third objective will be to specifically assess whether the TMS targets has a differential impact on state levels of craving relative to baseline (Tobacco Craving Questionnaire \[TCQ\]. The investigators plan to accomplish these three objectives using a randomized, controlled experiment involving 2 sessions.

Eligibility criteria

Qualifiers

Nicotine dependent individuals (according to the Alcohol, Smoking and Substance Involvement Screening Test nicotine dependence score).

Be between the ages of 18 and 55 years old.

Not received substance abuse treatment within the previous 30 days.

Be in stable mental and physical health.

Disqualifiers

Contraindication to MRI (e.g., presence of metal in the skull, orbits or intracranial cavity, claustrophobia).

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.

History or MRI evidence of neurological disorder that would lead to local or diffuse brain lesions or significant physical impairment.

Trial design

Treatments tested in this trial

  • Transcranial Magnetic Stimulation

Treatment groups

42 Participants
are divided into 2 treatment groups