ClinicalTrials.Veeva

Menu

TMS Modulation of Insula-related Brain Networks (TMS_INS)

Duke University logo

Duke University

Status

Completed

Conditions

Healthy Subjects

Treatments

Device: repeated transcranial magnetic stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT02689323
Pro00069059

Details and patient eligibility

About

The purpose of this study is to investigate the modulatory effects of repetitive transcranial magnetic stimulation (rTMS) on functional connectivity with the insula. Functional connectivity (FC) measures the interaction between brain regions, and recent neuroimaging studies have used FC to investigate how addiction affects FC among pertinent brain regions. rTMS, which can excite cortical neurons, has shown promise as a method to manipulate brain connectivity and could be used therapeutically to treat addiction. However, investigators first need more information on brain FC and how it relates to behavior, in order to guide rTMS target selection.

Enrollment

12 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. generally healthy
  2. between the ages of 18-55
  3. right-handed

Exclusion criteria

  1. significant health problems (e.g., current and uncontrolled liver, lung, or heart problems) or presence of medical illness likely to alter brain morphology (including history of seizure, history of epilepsy in self or first degree relatives, stroke, brain surgery, head injury, and known structural brain lesion)
  2. current diagnosis of Axis I psychiatric disorders (e.g., depression, anxiety disorder, schizophrenia)
  3. meet DSM-5 criteria for current substance use disorder other than nicotine
  4. use of psychoactive medications that would result in a positive urine drug screen
  5. Current use of medications known to lower the seizure threshold
  6. positive breath alcohol concentration
  7. presence of conditions that would make MRI unsafe (e.g., metal implants, pacemakers)
  8. among women, a positive urine pregnancy test
  9. vision that cannot be corrected to 20/40

Trial design

Primary purpose

Device Feasibility

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

12 participants in 1 patient group

Open label
Experimental group
Description:
Participants will undergo 5 sessions of active rTMS
Treatment:
Device: repeated transcranial magnetic stimulation

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems