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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02919423
Other study ID # Pro00077293
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 2016
Est. completion date January 25, 2018

Study information

Verified date January 2019
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date January 25, 2018
Est. primary completion date January 25, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- generally healthy

- between the ages of 18-55

- right-handed

Exclusion Criteria:

- 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)

- current diagnosis of Axis I psychiatric disorders (e.g., depression, anxiety disorder, schizophrenia)

- meet DSM-5 criteria for current substance use disorder other than nicotine

- use of psychoactive medications that would result in a positive urine drug screen

- Current use of medications known to lower the seizure threshold

- positive breath alcohol concentration

- presence of conditions that would make MRI unsafe (e.g., metal implants, pacemakers)

- among women, a positive urine pregnancy test

- vision that cannot be corrected to 20/40

Study Design


Related Conditions & MeSH terms


Intervention

Device:
transcranial magnetic stimulation


Locations

Country Name City State
United States Duke University Durham North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Functional Connectivity Strength Measured With Functional Magnetic Resonance Imaging Difference in functional connectivity from the TMS target site to the right insula. The primary dependent variable was the resting-state functional connectivity strength between the TMS target site and the right insula. baseline and 1 week
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