Actively Recruiting

Age: 35Years - 60Years
FEMALE
Healthy Volunteers
NCT07422987

GLP-1RA Effects on Lean Mass and Bone Health in Midlife Women

Led by University of Kansas Medical Center · Updated on 2026-02-20

50

Participants Needed

1

Research Sites

71 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is designed with the interest to learn on the effects of estrogen levels and how it affects body compositions and muscle function in midlife women who are taking a GLP-1RA for weight loss.

CONDITIONS

Official Title

GLP-1RA Effects on Lean Mass and Bone Health in Midlife Women

Who Can Participate

Age: 35Years - 60Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female gender
  • Age between 35 and 60 years
  • Body mass index (BMI) of 30 or higher, or BMI of 27 or higher with at least one cardiometabolic risk factor (dyslipidemia, hypertension, obstructive sleep apnea, metabolic syndrome, fatty liver, polycystic ovary syndrome)
  • Newly prescribed a GLP-1 receptor agonist medication
  • English speaking
  • Stable body weight for the past 6 months
Not Eligible

You will not qualify if you...

  • Pregnant women
  • Under 35 years or over 60 years old
  • Born male
  • Unable to provide informed consent
  • Cannot read or speak English
  • Diagnosis of type 2 diabetes
  • Discontinued GLP-1 receptor agonist medication less than 6 months ago
  • Contraindications to GLP-1 receptor agonist use, including personal or family history of medullary thyroid carcinoma, multiple endocrine neoplasia type 2, pancreatitis, pregnancy, drug hypersensitivity, or active suicidal thoughts
  • Currently taking aromatase inhibitors or selective estrogen receptor modulators (SERMs)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The University of Kansas Medical Center

Kansas City, Kansas, United States, 66160

Actively Recruiting

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Research Team

J

Johanna Finkle, MD

CONTACT

H

Holly Hull, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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