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NCT07480109 · ClinicalTrials.gov registry record · NA

Increased Dietary Protein Intake During GLP-1 Medication Use (in Middle-aged Women With Overweight/Obesity)

A NA study, sponsored by University of Texas at Austin.

Recruiting
Registry status
NA
Development phase
75
Enrollment target

NCT07480109: Recruiting NA study, sponsored by University of Texas at Austin.

NCT07480109 is a NA study that is actively recruiting participants, run by University of Texas at Austin. The registered enrollment target is 75 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07480109, a NA study, is actively recruiting participants, sponsored by University of Texas at Austin.

RECRUITING
Registry status
NA
Development phase
75 participants
Enrollment target

Study Summary

Middle-aged women with (overweight/)obesity who will begin or have begun GLP-1 medication use will be recruited to complete a 12-week diet intervention study. For 12-weeks, participants will continue to take their GLP-1 medication and may be provided with protein-rich foods to consume every day. Body composition, eating behavior, health, and well-being will be measured before and after the study.

Primary Outcome

Whole body total, fat, and fat free mass will be determined with Dual X-ray Absorptiometry (DXA). The DXA uses a linear X-ray fan beam with switched-pulse dual-energy and a multi-element detector array. The whole body scan takes \<1.8 sec with radiation exposure of 0.01mGy.

Interventions

  • BEHAVIORAL Protein Rich Foods

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2026-06-01
Est. Completion 2027-09-30
Phase NA
University of Texas at Austin

257 total trials

What NCT07480109 shows while recruiting

NCT07480109 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which Protein Rich Foods is the first listed.

NCT07480109 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07480109 about?

NCT07480109 is a clinical study titled "Increased Dietary Protein Intake During GLP-1 Medication Use (in Middle-aged Women With Overweight/Obesity)". Middle-aged women with (overweight/)obesity who will begin or have begun GLP-1 medication use will be recruited to complete a 12-week diet intervention study. For 12-weeks, participants will continue to take their GLP-1 medication and may be provided with protein-rich foods to consume every day. Bod...

What is the current status of trial NCT07480109?

This trial is currently recruiting. It is a NA study. The enrollment target is 75 participants. The study started on 2026-06-01. Estimated completion is 2027-09-30.

What interventions are being tested in trial NCT07480109?

The interventions under investigation include: Protein Rich Foods (BEHAVIORAL).

Who is sponsoring clinical trial NCT07480109?

This trial is sponsored by University of Texas at Austin, which has 257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07480109's enrollment target sits among peer trials

75 1069th of 2000 higher than 919 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07480109, the US trial registry maintained by the National Library of Medicine. NCT07480109 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.