Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
16 participants
INTERVENTIONAL
2023-07-15
2024-04-09
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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Low-Fat Pork
This condition will consist of consuming 90.2 g of low-fat (4.90% crude fat) ground pork.
95.1% Lean Pork
This intervention will contain 120 kcals, 4.4 g fat, and 20 g protein from low-fat ground pork.
High-Fat Pork
This condition will consist of consuming 109.6 g of high-fat (18.84% crude fat) ground pork.
81.16% Lean Pork
This intervention will contain 266 kcals, 20.6 g fat, and 20 g protein from high-fat ground pork.
Carbohydrate Control
This condition will consist of a carbohydrate beverage.
Carbohydrate Beverage
This intervention will contain 266 kcals and 73.3 g carbohydrate from a carbohydrate beverage.
Interventions
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95.1% Lean Pork
This intervention will contain 120 kcals, 4.4 g fat, and 20 g protein from low-fat ground pork.
81.16% Lean Pork
This intervention will contain 266 kcals, 20.6 g fat, and 20 g protein from high-fat ground pork.
Carbohydrate Beverage
This intervention will contain 266 kcals and 73.3 g carbohydrate from a carbohydrate beverage.
Eligibility Criteria
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Inclusion Criteria
* Pre-menopausal
* Recreationally active
* Weight stable for prior 6 months
Exclusion Criteria
* Pregnancy
* Irregular menstrual cycles
* Participation in previous research using \[13C6\]phenylalanine
* Participation in other ongoing research that interferes with this study (e.g., conflicting diet, activity interventions, etc.)
* Any hospitalization or surgery for a metabolic, cardiovascular, or neuromusculoskeletal complication within the past year
* Allergy or hypersensitivity to local anesthetics, latex, or adhesives (bandages, medical tape, etc.)
* Excess scarring after injury
* History of excess bleeding after cut
* Chronic or frequent dizziness/fainting, and arm or leg weakness/numbness
* Arthritis
* Tumors
* Mental Illness
* Hepatorenal, cardiovascular musculoskeletal, autoimmune, or neurological disease or disorder
* Predisposition to hypertrophic scarring or keloid formation
* Physical activity limitations
* Consumption of ergogenic-levels of dietary supplements that may affect muscle mass (e.g., creatine, HMB), insulin-like substances, or anabolic/catabolic pro-hormones (e.g., DHEA) within 6 weeks prior to participation
* Consumption of thyroid, androgenic, or other medications known to affect endocrine function
* Consumption of medications known to affect protein metabolism (e.g., prescription-strength corticosteroids, non-steroidal anti-inflammatories, or acne medication)
* Unwillingness to comply with study procedures
* Weight unstable (variation \>5% of bodyweight in last 6-12 months)
* Current or previous tobacco use with last 6 months
* Obesity (body mass index; BMI \> 30 kg/m\^2)
* Score of less than 14 or greater than 24 on Godin-Shephard Leisure-Time Physical Activity Questionnaire
* Phenylketonuria
* Anyone hospitalized previously for COVID-19 without a cardiovascular workup screening for cardiovascular issues post-infection
* Anyone recovering from COVID-19 infection within the preceding 10 days
20 Years
50 Years
ALL
Yes
Sponsors
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University of Illinois at Urbana-Champaign
OTHER
Responsible Party
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Principal Investigators
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Nicholas A Burd, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Illinois at Urbana-Champaign
Locations
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Louise Freer Hall (University of Illinois Urbana-Champaign)
Urbana, Illinois, United States
Countries
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References
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Zupancic Z, Askow AT, Barnes TM, Deutz MT, Ulanov AV, Dilger RN, Dilger AC, Willard JW, Mackenzie RW, Harseim JE, Hernandez-Saavedra D, Burd NA. Ingestion of a lipid-rich meat matrix blunts the postexercise increase of myofibrillar protein synthesis rates in healthy adults: a randomized controlled trial. Am J Clin Nutr. 2025 Sep 7:S0002-9165(25)00517-9. doi: 10.1016/j.ajcnut.2025.09.001. Online ahead of print.
Other Identifiers
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23257
Identifier Type: -
Identifier Source: org_study_id
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