Actively Recruiting
The Effects of Varying Protein Intakes on Muscle Protein Synthesis During Injury-Mediated Muscle Disuse
Led by United States Army Research Institute of Environmental Medicine · Updated on 2025-09-11
28
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how different amounts of dietary protein affect muscle protein synthesis in healthy, active adults who experience muscle disuse due to injury. The study focuses on overcoming muscle loss caused by reduced muscle use, which leads to a negative balance between muscle protein breakdown and synthesis. This work aims to identify the optimal protein dose to stimulate muscle rebuilding during periods of immobilization to improve recovery from musculoskeletal injuries. Participants will undergo a randomized, double-blind study where one leg is immobilized using a knee brace fixed at about 60 degrees of flexion for five days, while the other leg remains active as a control. During immobilization, diets will be standardized. After this phase, participants will consume either 20 grams or 40 grams of whey protein as a beverage to evaluate muscle protein synthesis responses in both legs. Throughout the study, participants will undergo stable isotope infusions, blood draws, and muscle biopsies to measure muscle protein synthesis rates. Researchers will assess how muscle responds to the protein doses after immobilization, using advanced methods like 2H5-Phenylalanine stable isotope techniques. The trial will help develop nutritional strategies to preserve muscle mass and support recovery after injury. The study includes careful monitoring of diet, physical activity, and safety, with participation lasting at least the immobilization and protein feeding phases.
CONDITIONS
Brief Title
Muscle Response to Different Amounts of Dietary Protein During Leg Immobilization
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men and women aged 18 to 39 years (17 to 39 years if military personnel)
- Body mass index (BMI) between 18.5 and 32 kg/m2
- Regularly participate in aerobic and/or resistance exercise at least 2 days per week
- Willing to avoid alcohol, smoking, nicotine products, and dietary supplements 24 hours before and during immobilization and testing
- Willing to only consume caffeine products provided by study staff during the study
- Supervisor approval for federal civilian employees and certain military personnel
- Biological females must have normal menstrual cycles or be on continuous hormonal contraception
You will not qualify if you...
- Musculoskeletal injuries that prevent safe use of crutches
- Personal or family history of thrombosis, deep vein thrombosis (DVT), or pulmonary embolism (PE)
- Metabolic, cardiovascular, gastrointestinal, neuromuscular disorders, lower-limb amputation, or muscle/bone wasting conditions
- Taking medications that affect macronutrient use (e.g., statins, corticosteroids, weight loss drugs)
- Abnormal blood clotting as determined by medical oversight
- Allergy to lidocaine or similar local anesthetics
- Current alcoholism, anabolic steroid use, or substance abuse
- Blood donation within 8 weeks before the study
- Pregnant, trying to become pregnant, or breastfeeding
- Unable or unwilling to follow study diets or physical restrictions
- Unable or unwilling to wear the knee brace and use crutches during immobilization
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 - 5 days
Participants undergo 5 days of unilateral leg immobilization using a rigid knee brace and ambulate with crutches while consuming standardized diets.
Daily visits or check-ins during immobilization
Duration - 1 day
Participants receive either 20 g or 40 g of whey protein and undergo stable isotope infusions, serial blood draws, and muscle biopsies to assess muscle protein synthesis.
1 visit (in-person) involving infusions, blood draws, and biopsies
Trial Site Locations
Total: 1 location
1
US Army Research Institute of Environmental Medicine
Natick, Massachusetts, United States, 01760
Actively Recruiting
Research Team
E
Emily E Howard, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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