Skip to main content
Clinical Trials/NCT05786521
NCT05786521CompletedPhase 4

The Effect of GLP1 Receptor Agonists on Physical Function, Body Composition, and Biomarkers of Aging in Older Overweight/Obese Adults With Insulin Resistance

The University of Texas Health Science Center at San Antonio1 site in 1 country20 target enrollmentStarted: April 1, 2023Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
Lean Body Mass Change

Study Overview

Brief Summary

Semaglutide is a medication approved by the US Food and Drug Administration (FDA) as an antihyperglycemic (a drug that reduces glucoses in those with diabetes) and for weight management. This new study will help find out what effects, semaglutide has on people who take the drug and the drug's effect on physical function, body composition, and aging.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
65 Years to 90 Years (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Older than 65
  • Have prediabetes or diabetes
  • BMI ≥ 27.0 kg/m2
  • Living independently (not in assisted living or nursing home)

Exclusion Criteria

  • Have heart disease
  • Have liver disease

Arms & Interventions

Semaglutide and lifestyle intervention

Experimental

Participants will meet with a dietician throughout the study to discuss lifestyle counseling based on recommendation in the diabetes prevention program. They will also be given semaglutide for 20 weeks.

Intervention: Semaglutide Injectable Product (Drug)

Semaglutide and lifestyle intervention

Experimental

Participants will meet with a dietician throughout the study to discuss lifestyle counseling based on recommendation in the diabetes prevention program. They will also be given semaglutide for 20 weeks.

Intervention: Lifestyle Counseling (Behavioral)

Lifestyle intervention

Active Comparator

Participants will meet with a dietician throughout the study to discuss lifestyle counseling based on recommendation in the diabetes prevention program

Intervention: Lifestyle Counseling (Behavioral)

Outcomes

Primary Outcomes

Lean Body Mass Change

Time Frame: Baseline to 20 weeks

Determine if there is any change in lean body mass

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tiffany Cortes

Assistant Professor

The University of Texas Health Science Center at San Antonio

Study Sites (1)

Loading locations...

Similar Trials

Effect of GLP1 Receptor Agonists on... | Clinical Trial