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Animal and Microbial-based Dietary Protein Efficiency in Adults (YPQ)

D

Daniel Moore

Status

Enrolling

Conditions

Protein Metabolism

Treatments

Dietary Supplement: Whey Protein Isolate Supplement
Dietary Supplement: Yeast Protein Supplement
Dietary Supplement: Collagen Hydrolysate Supplement

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT07148908
REB00048239

Details and patient eligibility

About

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.

Enrollment

13 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

13 participants in 3 patient groups

Yeast Protein Supplement
Experimental group
Description:
Participants will be consuming test beverage composed of yeast protein and their whole-body protein metabolism will be determined over the subsequent 8 hours.
Treatment:
Dietary Supplement: Yeast Protein Supplement
Whey Protein Isolate Supplement
Active Comparator group
Description:
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.
Treatment:
Dietary Supplement: Whey Protein Isolate Supplement
Collagen Hydrolysate Supplement
Active Comparator group
Description:
Participants will be consuming test beverage composed of collagen protein and their whole-body protein metabolism will be determined over the subsequent 8 hours.
Treatment:
Dietary Supplement: Collagen Hydrolysate Supplement

Trial contacts and locations

1

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Central trial contact

Daniel R. Moore, Ph.D.

Data sourced from clinicaltrials.gov

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