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ACTIVE NOT RECRUITING
NCT06861439
PHASE4

GLP-1s to Enhance Lasting Optimal Weight

Sponsor: Wake Forest University Health Sciences

View on ClinicalTrials.gov

Summary

The goal of this study is to examine how tirzepatide affects body composition, bone health, and physical performance in older adults over a nine-month period. Participants will take tirzepatide weekly, have clinic visits every 4 weeks, meet study doctor and registered dietitian every 4 weeks in person or video conference, attend group intervention sessions twice a month via video conference, weigh daily with a study-provided smart scale, keep a record of all foods and beverages consumed, and use a study-provided activity tracker to keep track of daily step counts.

Official title: Effects of Tirzepatide on Fat-Free Mass, Bone and Physical Function in Older Adults - a Pilot Study

Key Details

Gender

All

Age Range

65 Years - Any

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2025-07-07

Completion Date

2026-12-31

Last Updated

2025-10-28

Healthy Volunteers

No

Conditions

Interventions

DRUG

Tirzepatide

Tirzepatide will be initiated at a dose of 2.5 mg weekly and increased as tolerated to 5 mg weekly at four weeks for the remainder of the 9-month intervention period. Participants who are unable to tolerate the 5 mg dose will be decreased to the 2.5 mg dose.

Locations (1)

Wake Forest University Health Sciences

Winston-Salem, North Carolina, United States