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Animal and Microbial-based Dietary Protein Efficiency in Adults

The Effects of Animal- and Microbial-based Protein Sources on Whole-body Protein Metabolism in Healthy Adults

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07148908
Acronym
YPQ
Enrollment
13
Registered
2025-08-29
Start date
2025-07-01
Completion date
2025-12-31
Last updated
2025-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Protein Metabolism

Keywords

Protein quality, protein metabolism, stable isotopes, protein oxidation, indicator amino acid oxidation, protein synthesis

Brief summary

Given the relatively high carbon footprint and sustainability of animal-based proteins, there is a growing interest in determining the nutritional quality non-animal-based protein sources. The overall objective of this investigation is to examine the impact of different animal and microbial-based protein sources to support whole body protein synthesis in adults. To do this, investigators will employ a 'breath test' method developed in our laboratory as well as urine sampling. The results of this study will allow us to better understand the impact of dietary protein quality for maintaining health and body protein mass in adults.

Interventions

DIETARY_SUPPLEMENTYeast Protein Supplement

Each protein will be consumed at 0.9g/kg/d in n=8 hourly drinks

Each protein will be consumed at 0.9g/kg/d in n=8 hourly drinks

DIETARY_SUPPLEMENTCollagen Hydrolysate Supplement

Each protein will be consumed at 0.9g/kg/d in n=8 hourly drinks

Sponsors

Lesaffre International
CollaboratorINDUSTRY
Daniel Moore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Intervention model description

Single-blind randomized, counterbalanced design Thirteen healthy young (18-45 years of age, at least 6 females and 6 males) will be subjected to a non-invasive 13CO2 breath-test based on the indicator amino acid oxidation method and urine collections following hourly ingestion of protein test beverages (whey, yeast, and collagen randomized by trials).

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy, male and female, recreationally-active participants. * Healthy will be defined as screened by the PAR-Q+ (Appendix B) and The Physical Activity Readiness Questionnaire (Appendix C). * Participants will be aged 18-45 years old. * Participants are willing to abide by the compliance rules of this study. * Self-reported regular menstrual cycle (25-35d) within the last 3 months (female participants). * Use of monophasic combined oral contraceptives (COC) containing 21 active pills (e.g., Yaz, Marvelon, Cyclen, etc.; the brand of COC will be recorded) (female participants).

Exclusion criteria

* Inability to adhere to any of the compliance rules judged by principal investigator (e.g. dairy protein or yeast allergy). * Self-reported regular tobacco use. * Self-reported illicit drug use (e.g., growth hormone, testosterone, etc.). * Individuals who have participated in studies within the past year involving any of the stable isotopes in the study. * Use of multiphasic COCs due to the difficulty of controlling for hormonal fluctuations in such formulations (female participants). * Use of COCs containing \>21 active pills per cycle due to potential differences in their effect on metabolism (female participants). * Use of other forms of hormonal contraception (e.g., progestin-only pill, hormonal IUD, intravaginal ring) (female participants). * Not currently or previously (in the past 6 months) on a vegan diet

Design outcomes

Primary

MeasureTime frameDescription
1. Phenylalanine excretion (umol/kg/h)8 hoursWhole body phenylalanine excretion determined from the product of breath 13CO2 enrichment and carbon dioxide production rate (VCO2).
Phenylalanine oxidation (umol/kg/h)8 hoursWhole-body phenylalanine oxidation determined from the correction of phenylalanine excretion by the phenylalanine precursor enrichment determined from urine enrichment over the 8 hour measurement period.

Countries

Canada

Contacts

Primary ContactDaniel R. Moore, Ph.D.
drmoore@utoronto.ca416-946-4088

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026