Actively Recruiting
Exercise Impact on Dietary Protein Efficiency in Older Adults With Type 2 Diabetes
Led by University of Illinois at Urbana-Champaign · Updated on 2026-04-29
30
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
U
University of Illinois at Urbana-Champaign
Lead Sponsor
A
American Diabetes Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying older adults aged over 65, including those with type 2 diabetes (T2D) and controls, to understand how a 12-week progressive exercise program affects dietary protein efficiency. The study involves detailed pre- and post-testing to measure body composition, glucose tolerance, cardiovascular fitness, muscle performance, protein metabolism using stable isotope amino acid tests, and gut microbiota response. The goal is to see how exercise changes protein use and gut microbiome factors in people with and without diabetes. Participants will engage in moderate to vigorous aerobic and strength training two to three times weekly for 12 weeks. Strength training includes warm-ups on a stationary bike and exercises on leg and upper body machines, with intensity increasing based on individual comfort. Endurance training is performed on a stationary bike with heart rate and perceived exertion guiding progression over four 3-week phases, gradually increasing duration and effort. The study includes two groups: one with diagnosed T2D and one non-diabetic control group, both completing the same exercise and testing schedule. During the study, participants will complete questionnaires and undergo multiple assessments including submaximal aerobic tests, muscle strength and power tests, dietary protein metabolism trials involving blood, urine, and breath samples, and gut microbiome testing with blood draws and fecal sample collection. Psychological well-being is also evaluated during exercise sessions. Researchers will monitor changes from enrollment through the 12-week intervention to assess how exercise impacts protein efficiency and gut microbiota metabolites.
CONDITIONS
Brief Title
Exercise and Protein Efficiency in T2D
Who Can Participate
Eligibility Criteria
You may qualify if you...
- At least 65 years old
- Body mass index between 25 and 40 kg/m²
- Female participants must have a waist to hip ratio greater than 0.8
- Male participants must have a waist to hip ratio greater than 1.0
- Free from structured exercise during the previous 6 months
- Weight stable for the previous 6 months
- For the T2D group: diagnosed by a physician with HbA1c greater than 6.5%
- For the control group: normal blood sugar with HbA1c not exceeding 5.6% and fasting blood glucose at or below 99 mg/dL
You will not qualify if you...
- Uncontrolled diabetes (HbA1c over 10% or insulin prescription)
- Diagnosis of diabetic neuropathy or failing neuropathy screening
- Current use of statins
- Peripheral edema
- Use of dietary supplements affecting muscle mass or hormones within 6 weeks prior to participation
- Untreated hypothyroidism or epilepsy
- Use of medications affecting blood vessel function
- Possibility of pregnancy
- Any neurological, cardiovascular, or musculoskeletal disease preventing exercise testing
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Participants complete eligibility questionnaires electronically before enrollment.
Duration - Several days prior and including 2 separate testing days
Participants undergo baseline assessments including cardiorespiratory fitness, muscle performance, blood collection, and fecal sample collection after controlled diet and overnight fasting.
2 in-person visits for physical testing and blood sampling
Duration - 12 weeks
Participants engage in moderate to vigorous strength and endurance training 2-3 times per week with progressive intensity based on individual comfort.
Supervised exercise sessions 2-3 times per week
Duration - Several days after 12-week training
Participants repeat the preliminary testing procedures including blood and fecal sample collection and psychological evaluations to assess changes after the exercise intervention.
2 in-person visits for post-intervention testing
Trial Site Locations
Total: 1 location
1
Freer Hall - University of Illinois
Urbana, Illinois, United States, 61801
Actively Recruiting
Research Team
N
Nicholas Burd (Professor), PhD
G
Gena Irwin (Research Assistant), M.S
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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