Animal and Microbial-based Dietary Protein Efficiency in Adults
YPQ
The Effects of Animal- and Microbial-based Protein Sources on Whole-body Protein Metabolism in Healthy Adults
1 other identifier
interventional
13
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2025
CompletedFirst Submitted
Initial submission to the registry
August 22, 2025
CompletedFirst Posted
Study publicly available on registry
August 29, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedAugust 29, 2025
August 1, 2025
4 months
August 22, 2025
August 22, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
1. Phenylalanine excretion (umol/kg/h)
Whole body phenylalanine excretion determined from the product of breath 13CO2 enrichment and carbon dioxide production rate (VCO2).
8 hours
Phenylalanine oxidation (umol/kg/h)
Whole-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.
8 hours
Study Arms (3)
Yeast Protein Supplement
EXPERIMENTALParticipants will be consuming test beverage composed of yeast protein and their whole-body protein metabolism will be determined over the subsequent 8 hours.
Whey Protein Isolate Supplement
ACTIVE COMPARATORParticipants will be consuming test beverage composed of whey protein isolate and their whole-body protein metabolism will be determined over the subsequent 8 hours.
Collagen Hydrolysate Supplement
ACTIVE COMPARATORParticipants will be consuming test beverage composed of collagen protein and their whole-body protein metabolism will be determined over the subsequent 8 hours.
Interventions
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
Each protein will be consumed at 0.9g/kg/d in n=8 hourly drinks
Eligibility Criteria
You may qualify if:
- 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).
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Daniel Moorelead
- Lesaffre Internationalcollaborator
Study Sites (1)
Kinesiology & Physical Education
Toronto, Ontario, M5S 2C9, Canada
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
August 22, 2025
First Posted
August 29, 2025
Study Start
July 1, 2025
Primary Completion
October 31, 2025
Study Completion
December 31, 2025
Last Updated
August 29, 2025
Record last verified: 2025-08