Observational Study of Anti-Obesity Medications
This study is looking at the real-world effects of anti-obesity medications like semaglutide and tirzepatide in adults managing their weight. Researchers want to understand how these medications change your body composition (like lean muscle and fat), muscle strength, and what you eat. They will also look at how your lifestyle, such as exercise, affects these changes. You could join if you are 18 or older and starting treatment with semaglutide or tirzepatide through Vineyard Virtual Health Clinic. To be eligible for these medications, you must have a Body Mass Index (BMI) of 30 or higher, or a BMI of 27 or higher with at least one related health condition. This is an observational study, meaning researchers will watch and collect information without giving you a specific intervention.
- Study design
- This is an observational study aiming to enroll 100 participants. It is not a randomized trial, meaning participants are not assigned to different treatment groups by chance.
- What's involved
- You would undergo periodic body composition and muscular performance tests. You would also complete online surveys about your nutrition and physical activity.
- Compensation
- Not stated in the trial record.
- Follow-up
- Follow-up assessments are conducted approximately 6 months and 17 months after your initial assessment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Study of Patients Being Treated With Anti-obesity Medication
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Change in Total Lean Soft TissueFrom baseline assessment to last available time point (follow-up assessments conducted ~6 months and ~17 months after baseline).
Change in total lean soft tissue assessed by dual-energy X-ray absorptiometry.
- Change in Appendicular Lean Soft TissueFrom baseline assessment to last available time point (follow-up assessments conducted ~6 months and ~17 months after baseline).
Change in appendicular lean soft tissue assessed by dual-energy X-ray absorptiometry.
- Change in Total Fat MassFrom baseline assessment to last available time point (follow-up assessments conducted ~6 months and ~17 months after baseline).
Change in total fat mass assessed by dual-energy X-ray absorptiometry.
- Change in Handgrip StrengthFrom baseline assessment to last available time point (follow-up assessments conducted ~3, ~6, and ~17 months after baseline).
Change in maximal handgrip strength as determined by a handgrip dynamometer.