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Clinical Trial Summary

Randomized controlled trial of an exposure-based behavioral treatment (CBT) in adults with functional dyspepsia who meet criteria for avoidant/restrictive food intake disorder (ARFID) with weight loss.


Clinical Trial Description

The purpose of this study is to conduct a randomized controlled trial (RCT) of a cognitive-behavioral treatment (CBT) compared to usual care as the control with adults with functional dyspepsia who also meet criteria for avoidant/restrictive food intake disorder (ARFID). Participants randomized into the CBT group will receive eight 1-hour sessions delivered weekly via the MGH-approved secure video platform Enterprise Zoom while the usual care group will be allowed to continue with treatment they are already receiving at the time of randomization. Participants in the usual care group will be offered CBT after study participation. We will determine the feasibility and acceptability of the CBT and explore changes in clinical outcomes and preliminary mechanisms. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05587127
Study type Interventional
Source Massachusetts General Hospital
Contact Blythe Peterson, BS
Phone 617-643-7884
Email GIbehavioralresearch@mgh.harvard.edu
Status Recruiting
Phase N/A
Start date November 30, 2022
Completion date August 2026

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