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GLP-1 Users' diets under the microscope: what are they really eating?

NCT ID NCT07313384

First seen Jan 04, 2026

Summary

This study follows 50 adults who are about to start GLP-1 therapy for obesity or type 2 diabetes. Researchers will track how their eating habits change over 12 weeks using diet quality scores and body weight. The goal is to understand what dietary support people need while on these medications, since current guidance focuses mostly on cutting calories rather than ensuring good nutrition.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Prisma Health Weight Management Institute

    RECRUITING

    Greenville, South Carolina, 29607, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

    Contact

    Contact Email: •••••@•••••

    Contact

    Contact

  • University South Carolina

    ENROLLING_BY_INVITATION

    Columbia, South Carolina, 20208, United States

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

GLP-1 therapy (a class of medications for obesity or type 2 diabetes)

What this could lead to

If successful, this study could help develop better dietary guidelines and support programs for people taking GLP-1 medications.

What could go wrong

This is a small observational study (50 people) that does not test a new treatment. It only looks at eating habits, so it cannot prove whether any diet changes improve health outcomes.

Conditions

The condition(s) this trial relates to.

Obesity obesity disorder type 2 diabetes mellitus

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.