GLPwatch

Clinical and Neurobehavioral Changes With Weight Loss Drug Discontinuation and Reinitiation

NCT07387796 · Not yet recruiting

Last updated 2026-05-28

This trial tests how stopping and restarting the weight loss drug tirzepatide affects brain responses to food cues in adults with substance use disorders or eating behavior changes.

Status Not yet recruiting Approved but enrollment has not started.
Phase Not applicable Not a phased drug trial (e.g. a device or behavioral study).
Type Interventional (clinical trial)
Design open-label (no blinding) basic-science study
Participants 40 people Planned (estimated).
Who can join Ages 18–70 · all sexes
Timeline Started 2026-06 · est. completion 2029-02
Where 1 site · United States

What this study is testing ClinicalTrials.gov NCT07387796 ↗

Description as written by the study sponsor.

The goal of this clinical study with research procedures is to learn how stopping and restarting tirzepatide (a medication that helps regulate blood sugar and appetite) affects brain activity, behavior, and health in adults ages 18-70 who are currently taking tirzepatide. Specifically, the study aims to examine how a short pause in tirzepatide affects hunger, mood, sleep, and daily functioning; how stopping and restarting tirzepatide alters brain chemistry and brain responses to food-related images; and how these changes relate to health measures such as quality of life and emotional well-being. There is no comparison group; instead, researchers will assess changes within each participant across three time points: while taking tirzepatide, after stopping it for 3-4 weeks, and after restarting it for 6-8 weeks. Participants will attend three in-person visits lasting approximately 3-4 hours each, during which they will complete interviews, questionnaires, and cognitive tasks; provide a urine sample (pregnancy screening for females); undergo a brain scan using magnetic resonance imaging (MRI) and MR spectroscopy (MRS); and receive a kit to provide a small stool sample. Participants will also complete two brief check-in phone calls between visits and the online BrainHealth Index between sessions, which includes surveys and cognitive tasks. All changes to tirzepatide use will occur under the supervision of a study physician to support participant safety and comfort, and the total study duration is approximately 13 weeks.

Treatments tested

Main thing measuredChange From On-Treatment to Discontinuation and Re-Initiation in Food Cue-Evoked BOLD Response in Reward and Salience Brain Regions
SponsorThe University of Texas at Dallas
Conditions studiedDrug Discontinuation, Substance Use Disorders, Eating Behavior Changes, Tirzepatide
GLP-1 drugs tirzepatide

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07387796 ↗