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Study identifier: NCT05700058 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Assessing the Dose-response of Muscle Protein Synthesis to "Super-whey" in Older Adults

Condition: Sarcopenia  ·  Sponsor: University of Nottingham

PhaseNA
Planned participants30
Who can joinMale, 65 Years to 85 Years
Healthy volunteersYes

About this study

Skeletal muscle accounts for approximately 45-55% of total body mass in healthy adults and plays a pivotal role in whole-body metabolic health, locomotion and physical independence. Undesirable loss of skeletal muscle mass (atrophy) is, however, a common feature of many diseases and scenarios including ageing, bed rest/immobilisation, cancer and physical inactivity. Despite the exact mechanisms causing muscle atrophy being not yet fully understood, "anabolic resistance" (reduced muscle building in response to protein feeding and exercise) is thought to be key, especially for age-related skeletal muscle losses (known as sarcopenia). As such, the search for optimal strategies (e.g., exercise and/ or nutritional interventions) to combat this anabolic blunting remains a hot-topic in scientific research. Leucine, an essential and branched chain amino acid (EAA/BCAA), is thought to be the most potent AA for stimulating muscle protein synthesis (MPS; the muscle building process). Although, as a stand-alone supplement, leucine is unlikely to provoke a robust and prolonged state of MPS, low doses of leucine-enriched mixed-EAAs can elicit similar increases in MPS as compared to a large dose of whey protein. As reduced appetite and increased satiety (feeling fuller) are common with advancing age, supplementation of a low-dose protein (i.e., leucine-enriched) that can adequately stimulate MPS may contribute to muscle health maintenance in older adults and reduce satiation following a me…

This description comes directly from the study's public registry record.

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Locations (1)

Centre of Ageing, Metabolism and PhysiologyDerby, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT05700058