RecruitingNot ApplicableNCT07104539

Strength Training Response of Muscle in GLP-1 Users


Sponsor

Virginia Polytechnic Institute and State University

Enrollment

30 participants

Start Date

Oct 8, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

GLP-1 medication is being prescribed for weight loss. However, GLP-1 medication may adversely affect muscle mass and muscle function. Moreover, any loss of muscle mass or muscle function with GLP-1 treatment may impair balance and increase fall risk. This is a particular concern among older adults already susceptible to the common muscle strength and muscle function loss with age, yet there is little evidence among this population. This study will address a gap in knowledge regarding the effects of GLP-1 treatment on muscle mass, muscle function, and balance/fall risk among adults age 50 and older.


Eligibility

Min Age: 50 Years

Inclusion Criteria4

  • Age, 50y+
  • Be taking GLP-1 medicine (Weygovy or Zepbound) for 1 month or less
  • Weight <300 lb
  • Pass a health and exercise readiness screening

Exclusion Criteria5

  • Age <50
  • Weight >300 lb
  • Osteoporosis
  • Active metabolic, neoplastic, or cardiovascular disease
  • Unable or unwilling to provide consent

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALStrength Training

Participants taking a GLP-1 will undergo a 14-week strength training regimen to determine changes in muscle mass. They will perform a series of resistance training exercises supervised by a personal trainer on 3 days per week.

OTHERWait first, then strength training

Participants will be waitlisted and receive the 14-week strength training intervention at the end of the waitlist period. During the waitlist period, participants will get no intervention and then be offered the strength training intervention after the first 14 weeks.


Locations(1)

Virginia Tech

Blacksburg, Virginia, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07104539


Related Trials