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Clinical Trial Summary

The aim of this mixed methods, single-group, single-center study will be to examine the feasibility of a food response training (FRT). This study will be conducted in patients with obesity recruited from NYU Langone Health. Measurements will occur at screening, baseline, and 3 months, for a subgroup of participants for we will collect saliva samples for genetic analysis at baseline assessment (ancillary study).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05203718
Study type Interventional
Source NYU Langone Health
Contact Sandra Wittleder, PhD
Phone 212-263-4149
Email Sandra.wittleder@nyulangone.org
Status Recruiting
Phase N/A
Start date November 9, 2022
Completion date October 2024

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