Recruiting

Tirzepatide

Sponsor:

The University of Texas at Dallas

Code:

NCT07387796

Conditions

Drug Discontinuation

Substance Use Disorders

Eating Behavior Changes

Tirzepatide

Eligibility Criteria

Sex: All

Age: 18 - 70

Healthy Volunteers: Not accepted

Interventions

Discontinuation and Reinitiation of Tirzepatide

Study Details

Brief summary:

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.

Conditions

Drug Discontinuation

Substance Use Disorders

Eating Behavior Changes

Tirzepatide

Study ID

NCT07387796

Start date

Oct, 2026

Status verified date

Sep, 2026

Completion date

Feb, 2029

Anticipated

Primary completion date

Feb, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Aged 18-70 years.
  • Currently on tirzepatide.
  • Currently receiving care from University of Texas- Southwestern (UTSW) Weight Wellness Clinic.
  • Cognitively capable of understanding and signing informed consent.
  • Be proficient in English.

Exclusion Criteria:

  • History of major neurological or psychiatric disorders, including substance use disorders that might confound brain imaging results (e.g., stroke, epilepsy, multiple sclerosis, schizophrenia, major depression requiring hospitalization).
  • Diagnosis of Type 2 Diabetes.
  • Current diagnosis of an eating disorder.
  • Use of medications affecting weight other than tirzepatide.
  • Pregnancy or breastfeeding.
  • MR contraindications:
  • Heart pacemaker, heart valve replacement, or aortic clips
  • Metal fragments in the eyes, skin, or elsewhere in the body
  • Brain clips or pieces of metal used in aneurysm surgery or intercranial bypass
  • Venous umbrella
  • Pieces of metal in the body resulting from work as a sheet-metal worker or welder
  • Clips placed in an internal organ
  • Prosthetic devices, such as middle ear, eye, joint, or penile implants
  • Joint replacement
  • Hearing aid that cannot be removed
  • Neurostimulator
  • Insulin pump
  • Shunts or stents
  • Metal mesh or coil implants
  • Metal plate, pin, screws, or wires, or any other metal implants

Study Design

Enrollment

40 participants

Anticipated

Intervention Model

Single group

Primary purpose

Basic Science

Interventions and Outcome Measures

Arms

experimental: Tirzepatide Discontinuation and Re-Initiation Arm

Participants in this single-group arm will complete three study visits that occur while they are taking tirzepatide, during a 3-4 week pause from the medication, and after they restart tirzepatide for 6-8 weeks. All medication changes are supervised by a study physician. At each visit, participants will complete interviews, questionnaires, cognitive tasks, magnetic resonance imaging (MRI) brain scans, and provide stool samples. They will also complete two short check-in phone calls and an online BrainHealth Index assessment between visits.

Interventions

Discontinuation and Reinitiation of Tirzepatide

Participants will temporarily pause their tirzepatide medication for 3-4 weeks and then restart it for 6-8 weeks under the supervision of a study physician. The medication change is done only for research purposes to study how stopping and restarting tirzepatide affects brain activity, appetite, mood, and other health measures. During this period, participants will complete MRI scans, behavioral assessments, questionnaires, and provide stool samples across three study visits.

Primary outcome measure

  • Change From On-Treatment to Discontinuation and Re-Initiation in Food Cue-Evoked BOLD Response in Reward and Salience Brain Regions [ Time Frame: Baseline (on tirzepatide), 3-4 weeks of discontinuation, and 6-8 weeks of re-initiation ]

Central Contacts and Locations

Central contacts

Samuel H Poelker-Wells, Master of Science

972-883-3375sxp230129@utdallas.edu

Aishwarya Veerkumar, Master of Public Health

972-883-3304Aishwarya.Veerkumar@UTDallas.edu

Locations

Center for BrainHealth

Recruiting

Dallas, Texas, United States, 75235

Contacts

Samuel M Poelker-Wells, Master of Science

972-883-3375sxp230129@utdallas.edu

Aishwarya Veerkumar, Master of Science

Aishwarya.Veerkumar@UTDallas.edu

More Information

Sponsor

The University of Texas at Dallas

Last update posted

Sep 2, 2026

Last verified

Sep, 2026

Keywords

  • Tirzepatide
  • Drug Discontinuation
  • Substance Use Disorders
  • Eating Behavior Changes

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by The University of Texas at Dallas on 2026-09-02.