About this trial
The purpose of this study is to determine how anabolic sensitivity, in response to the ingestion of a liquid protein meal, differs across the lifespan, between biological sexes, and with varying physical activity levels.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Healthy will be defined as screened by the PAR-Q+ (The Physical Activity Readiness Questionnaire for everyone)
Chronological age for Healthy Young (age: 18-35 years) or Older (age: 60-80 years) adults
Chronological age between 8 to 16 years, with maturity offset < -1 year from age of Peak Height Velocity (aPHV) for children and between -0.5 to +1.5 years from aPHV in adolescent participants
BMI between normal to overweight (18.5 - 29.9 kg/m2)
Disqualifiers
Regular use of nonsteroidal anti-inflammatory dugs (with the exception of daily low-dose aspirin)
use of anticoagulants
use of a walker, cane, or assistive walking device
infectious or gastrointestinal disease
Trial population
Convenience sample of individuals who qualify for the corresponding cohorts based on inclusion/exclusion criteria stated.
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Amino acid oxidation and net protein balance
Amino acid oxidation and net protein balance assessed by oral 1-13C Leucine tracer. Net protein balance is derived from the difference between amino acid intake (known) and total amino acid oxidation over the 6h post-prandial measurement period.
Sponsors and contacts
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