Timing (AM v PM) of Acute Resistance Exercise on Glycemic Control in Older Adults: The Acute T-Rex Study

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The primary aim of this study is to evaluate if a single bout of AM vs PM resistance exercise has different effects on insulin sensitivity and sleep. A randomized cross-over trial be used to compare resistance exercise at two different times of the day. Each condition will take place in a laboratory setting. Each condition will consist of exercise, overnight sleep, and oral glucose tolerance tests the following day. The AM exercise will occur \ 1.5 hours after habitual wake, and PM exercise will occur \ 11 hours after habitual wake. After a 2-6 week washout, participants will complete the other condition. The hypothesis is that PM exercise will be more beneficial than AM exercise in improving insulin sensitivity. This study could identify if there is a better time of day to perform resistance exercise to decrease risk of developing Type 2 Diabetes Mellitus.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 74
Healthy Volunteers: f
View:

• Men and women, all ethnicities, aged 50-74 years

• BMI ≥25 kg/m² and \<45 kg/m²

• Weight stable (less than 5% change in the past 6 months)

• Generally healthy individuals

• Not meeting recommended activity guidelines for aerobic or resistance exercise

Locations
United States
Utah
University of Utah HPER E Buildling
RECRUITING
Salt Lake City
Contact Information
Primary
Tanya M Halliday, PhD
tanya.halliday@utah.edu
801-213-1364
Backup
Study Email Study Email
trexstudy@utah.edu
8014487897
Time Frame
Start Date: 2023-11-15
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 20
Treatments
Experimental: AM Resistance Exercise
Resistance Exercise intervention taking place in the AM
Experimental: PM Resistance Exercise
Resistance Exercise intervention taking place in the PM
Related Therapeutic Areas
Sponsors
Leads: University of Utah

This content was sourced from clinicaltrials.gov

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