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Clinical Trials/NCT02362542
NCT02362542
Completed
Not Applicable

Effect of Transcranial Direct Current Stimulation (tDCS) on Appetite Control Related Brain Regions

Chungbuk National University1 site in 1 country15 target enrollmentFebruary 2015
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Chungbuk National University
Enrollment
15
Locations
1
Primary Endpoint
Regional brain activity measured by blood-oxygen-level dependent (BOLD) signal of functional MRI
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to investigate the effect of Transcranial Direct Current Stimulation (tDCS) on appetite control related brain regions.

Detailed Description

Transcranial direct current stimulation (tDCS) is emerging tool for brain modulation in a variety of clinical conditions. In addition, recent neuroimaging studies suggest that modifying the activity of brain circuits involved in eating behavior could provide therapeutic benefits in obesity. The investigators aim to assess whether modulation of the dorsolateral prefrontal cortex (DLFPC) using tDCS, modifies behavioral response and brain activity while watching visually presented food cues in obese subjects. Subjects will receive tDCS two times, one is active stimulation and the other is sham stimulation. Both stimulations will be separated at least one week and the order of sham and active tDCS will be counterbalanced across subjects. Subjects will perform functional MRI experiments with visual food cues. Questionnaire with behavior measures, body compositions, blood tests will be performed.

Registry
clinicaltrials.gov
Start Date
February 2015
End Date
October 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hyung Jin Choi

Clinical Assistant Professor

Chungbuk National University

Eligibility Criteria

Inclusion Criteria

  • BMI \> 28 kg/m2

Exclusion Criteria

  • history of brain trauma, epilepsy, or other neurological problems

Outcomes

Primary Outcomes

Regional brain activity measured by blood-oxygen-level dependent (BOLD) signal of functional MRI

Time Frame: Immediately after intervention

3T MR scanner with Echo Planar Imaging(EPI) capability(Magnetom, Siemens Medical System)

Secondary Outcomes

  • Behavior outcomes on the visual analog scale(Immediately after intervention)

Study Sites (1)

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