Skip to main content
Clinical Trials/NCT02362633
NCT02362633
Completed
Not Applicable

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

Chungbuk National University1 site in 1 country27 target enrollmentFebruary 2015
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Chungbuk National University
Enrollment
27
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 long-term 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 long-term modulation of the dorsolateral prefrontal cortex (DLFPC) using tDCS, modifies behavioral response and brain activity while watching visually presented food cues and taste cues in obese subjects. Subjects will be randomly divided into sham and real tDCS arms. Subjects will receive sham or real tDCS ten times. Subjects will be investigated before and after sham or real tDCS interventions. Subjects will perform functional MRI experiments with visual and taste 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
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hyung Jin Choi

Clinical Assistant Professor

Chungbuk National University

Eligibility Criteria

Inclusion Criteria

  • BMI \> 26 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: Day 14 (After ten interventions)

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

Secondary Outcomes

  • Behavior outcomes on the visual analog scale(Day 14 (After ten interventions))

Study Sites (1)

Loading locations...

Similar Trials