Cortical rTMS as a Tool to Change Brain Reactivity to Alcohol Cues

NCT02939313 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 71

Last updated 2022-01-13

No results posted yet for this study

Summary

The goal of this investigation is to determine if, in heavy alcohol users, a single session of transcranial magnetic brain stimulation (TMS) over a brain region involved in craving (medial prefrontal cortex) and a brain region involved in cogntive control (dorsolateral prefrontal cortex) can lower an individual's craving and brain response to alcohol cues. This study involves a screening visit, followed by three visits which involve brain imaging (using functional MRI) and brain stimulation (using TMS). There is also an additional Magnetic resonance spectroscopy (MRS) exploratory Aim in which we will measure the concentration of glutamate in the prefrontal cortex before and after a session of TMS.

Conditions

  • Alcohol Dependance

Interventions

DEVICE

medial prefrontal cortex

a form of theta burst stimulation that noninvasively induces a depression in brain reactivity

DEVICE

dorsolateral prefrontal cortex

a form of transcranial magnetic stimulation that noninvasively induces an increase in brain reactivity

DEVICE

sham

sham stimulation

Sponsors & Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

    collaborator NIH
  • Medical University of South Carolina

    lead OTHER

Principal Investigators

  • James Prisciandaro, Ph.D. · Medical University of South Carolina

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
21 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2021-04-12
Completion
2021-04-12

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02939313 on ClinicalTrials.gov