Actively Recruiting
Muscle Response to Different Amounts of Dietary Protein During Leg Immobilization
Led by United States Army Research Institute of Environmental Medicine · Updated on 2025-09-11
28
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Individuals who sustain musculoskeletal injuries (MSKI) can experience a rapid loss of muscle mass due to declines in muscle loading and activation that occur post-injury (i.e., disuse atrophy). Loss of muscle under these conditions is attributed to a persistent negative net muscle protein balance (muscle protein synthesis \[MPS\] \< muscle protein breakdown) that results, in part, from declines in postprandial MPS (i.e., anabolic resistance). Nutritional interventions that enhance postprandial MPS may be used to overcome disuse-induced anabolic resistance and preserve muscle mass to accelerate recovery and improve recovery outcomes. While supplemental protein has been explored as a potential countermeasure to disuse-induce anabolic resistance, the observed efficacy of such interventions has been mixed. Equivocal findings across studies may be attributed, in part, to an insufficient understanding of what constitutes an effective protein-based intervention. Importantly, no study to date has determined an optimal protein dose for overcoming disuse-induce anabolic resistance, or if there is a threshold for maximally stimulating postprandial MPS under disuse conditions. Therefore, the objective of this work is to determine rates of MPS at rest and in response to standard (20 g) or high (40 g) doses of whey protein during knee immobilization (DISUSE) compared with standard activity (ACTIVE)
CONDITIONS
Official 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 final testing
- Willing to consume only caffeine products provided by study staff during the study
- Supervisor approval for federal civilian employees and non-SRV active-duty military personnel stationed at NSSC
- Biological females must have normal menstrual cycles between 26 and 32 days in length with 5 cycles in the past 6 months or be on continuous hormonal contraception (IUD or oral contraceptives without placebo)
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 disorders
- Use of medications affecting 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 issues
- Blood donation within 8 weeks before the study
- Pregnant, trying to become pregnant, or breastfeeding
- Unwilling or unable to consume study diets or foods due to preferences or allergies
- Unwilling or unable to follow physical activity restrictions during immobilization and final testing
- Unwilling or unable to keep the knee brace on and use crutches during immobilization
AI-Screening
AI-Powered Screening
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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
CONTACT
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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