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Clinical Trial Summary

The purpose of this research is to conduct a randomized controlled trial (RCT) assessing the impact of CBT on neural responses to binge eating stimuli.


Clinical Trial Description

Females with a BMI>/=25 kg/m2 and BED will be randomized to either a 16-week, one-on-one CBT intervention (n=20) or a waitlist control (WL; n=20). Both groups will have blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) scans at baseline and after the 16-week intervention. During the scans, participants will complete the following tasks: 1) food-specific stop signal task (SST), and 2) script-driven imagery of binge foods. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03604172
Study type Interventional
Source University of Pennsylvania
Contact
Status Completed
Phase N/A
Start date August 8, 2018
Completion date November 22, 2021

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