Actively Recruiting
Impact of Food Combinations on the Stimulation of Post-exercise Muscle Protein Synthesis in Healthy Adults
Led by University of Illinois at Urbana-Champaign · Updated on 2026-05-01
15
Participants Needed
2
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how different food combinations affect muscle protein synthesis after exercise in healthy, recreationally active young adults aged 19 to 40 years. This trial uses a semi-crossover randomized design to compare the effects of meals containing russet potato and lean ground beef, white bread and lean ground beef, or lean ground beef alone on muscle protein building and amino acid metabolism. The goal is to understand how these foods influence muscle health and protein metabolism following resistance exercise. Participants will perform a single session of resistance exercise involving leg press and leg extension. Immediately after exercise, they will consume one of three meals: a combination of baked russet potato with skins and lean ground beef, white bread with lean ground beef, or lean ground beef alone. Stable isotope tracers will be infused intravenously to track amino acid use and muscle protein synthesis. Muscle biopsies and blood samples will be collected to measure protein synthesis rates and anabolic signaling during the trials. Participants will undergo preliminary testing including body measurements, resting metabolic rate, diet recording, and strength testing before the infusion trials. During the trials, blood samples and muscle biopsies will be taken at multiple time points to assess protein metabolism. Daily physical activity will be monitored with accelerometers, and participants will follow dietary and exercise restrictions before each trial. The study will measure muscle protein fractional synthesis rate and whole body leucine kinetics as primary outcomes to evaluate the effects of these food combinations.
CONDITIONS
Brief Title
Diet Synergy in Muscle Protein Synthesis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 19-40 years
- Pre-menopausal
- Recreationally active
- Stable weight for the prior 6 months
You will not qualify if you...
- Age outside of 19-40 years
- Pregnancy
- Irregular menstrual cycles (around 21 or 35 day cycle)
- Previous participation in research using L-[1-13C] leucine and L-[ring-2H5] phenylalanine
- Participation in other ongoing research that conflicts with this study (e.g., diet or activity interventions)
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.
1 visit (in-person)
Duration - 1 day
Participants complete preliminary assessments including informed consent, body measurements, blood pressure, body composition scan, resting metabolic rate test, strength testing, and receive an accelerometer to wear prior to infusion trials.
1 visit (in-person)
Duration - Each trial lasts several hours with at least 7 days between trials
Participants complete two infusion trial sessions, each starting with fasting and dietary recording, followed by stable isotope infusions, multiple blood collections, muscle biopsies, resistance exercise, and ingestion of assigned food combinations to study muscle protein synthesis.
2 visits (in-person) separated by at least 7 days
Duration - 2 to 4 days after each infusion trial
Participants receive post-biopsy care instructions and are contacted the day after each trial to check on the healing process of biopsy sites.
2 follow-up contacts (remote or in-person)
Trial Site Locations
Total: 2 locations
1
Louise Freer Hall
Urbana, Illinois, United States, 61801
Not Yet Recruiting
2
Louise Freer Hall
Urbana, Illinois, United States, 61801
Actively Recruiting
Research Team
N
Nicholas A Burd (Full Professor), PhD
C
Calvin Chen, PhD Student
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
3
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