GLP-1 Analogue Effects on Food Cues, Stress, Motivation for Highly Palatable Foods, and Weight
Completed · Phase 1 · Has a placebo group
Conditions studied: Obesity
In brief
To examine response to a glucagon-like peptide-1 analogue vs. placebo in patients with obesity and assess impact on craving, hunger, stress, and weight outcomes.
Key facts
- Study ID
- NCT04779697
- Run by
- Yale University
- People needed
- 96
- Starts
- 2021-02-01
- Expected to finish
- 2024-11-19
- Last updated by the study team
- 2026-02-10
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- BMI ranging from 30-49.9 kg/m2
- No significant medical problems, including diabetes
- No history of HgbA1c <6.5%
- English speaking and able to read English and complete study evaluations
- Able to provide informed written and verbal consent
You may not qualify if…
- Any significant current medical conditions, including neurological, renal, thyroid, cardiovascular, liver, endocrine or immune conditions, including diagnosis of T2DM or T1DM by American Diabetes Association (ADA) criteria
- Meet current or past DSM-IVR criteria for alcohol dependence or any substance use disorders, including nicotine, or psychiatric disorders, including eating disorders, or use of any psychiatric medications, including anxiolytics, antidepressants, naltrexone or antabuse, anti-smoking medications
- Current active participation in a weight loss program or weight loss of >10% of total body weight during the prior 6 months
- Taking any other anti-obesity medication
- History of pancreatitis, medullary thyroid cancer, or MEN syndrome, or (6) women who are pregnant or lactating, or peri/postmenopausal
Where it is running
- The Yale Stress Center: Yale University — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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