NCT07148908

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
13

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 22, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 29, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

August 29, 2025

Status Verified

August 1, 2025

Enrollment Period

4 months

First QC Date

August 22, 2025

Last Update Submit

August 22, 2025

Conditions

Keywords

Protein qualityprotein metabolismstable isotopesprotein oxidationindicator amino acid oxidationprotein synthesis

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

EXPERIMENTAL

Participants will be consuming test beverage composed of yeast protein and their whole-body protein metabolism will be determined over the subsequent 8 hours.

Dietary Supplement: Yeast Protein Supplement

Whey Protein Isolate Supplement

ACTIVE COMPARATOR

Participants will be consuming test beverage composed of whey protein isolate and their whole-body protein metabolism will be determined over the subsequent 8 hours.

Dietary Supplement: Whey Protein Isolate Supplement

Collagen Hydrolysate Supplement

ACTIVE COMPARATOR

Participants will be consuming test beverage composed of collagen protein and their whole-body protein metabolism will be determined over the subsequent 8 hours.

Dietary Supplement: Collagen Hydrolysate Supplement

Interventions

Yeast Protein SupplementDIETARY_SUPPLEMENT

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

Yeast Protein Supplement

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

Whey Protein Isolate Supplement

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

Collagen Hydrolysate Supplement

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Study Sites (1)

Kinesiology & Physical Education

Toronto, Ontario, M5S 2C9, Canada

RECRUITING

Central Study Contacts

Daniel R. Moore, Ph.D.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Model Details: 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).
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

Locations