Glucose- en botmetabolisme bij gezonde mensen N/A
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Age >=20 and =18.5 and
Exclusion criteria
Exclusion criteria: • Blood donation during the study period • Currently smoking • Consumption of >21 alcoholic beverages per week • Use of illicit drugs • Regular use of protein supplements. • A self-reported reported lactose intolerance, allergy or sensitivity to dairy ingredients • Reported slimming or medically prescribed diet • Use of antibiotics in the past month • Medical condition that can interfere with the study outcome (i.e. cardiovascular disease, pulmonary disease, rheumatoid arthritis, orthopaedic disorders, renal disease, liver disease, diabetes mellitus, inflammatory disease, cognitive impairment, and thyroid or parathyroid disease) • Use of medications known to interfere with selected outcome measures (i.e. corticosteroids) • (Chronic) injuries of the locomotor system that can interfere with the intervention. • Current participation in another biomedical research study. • Trained individuals (i.e. performing sport activities for more than 6 hours per week). • Structural or competitively participating in exercise/ sports with a substantial high-impact component, such as soccer, volleyball, running, and lower body resistance training.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-prandial metabolic response as assessed by amino acids concentrations, and the bone formation marker procollagen type I N propeptide | — |
Secondary
| Measure | Time frame |
|---|---|
| Post-prandial metabolic response as assessed by glucose metabolism (glucose, insulin, GLP-1) and bone metabolism (calcium, PTH, CTX). Hunger and satiety will be assessed by means of a VAS scale. | — |
Countries
Netherlands