Status:

COMPLETED

Protein Requirements in Resistance Trained Females

Lead Sponsor:

University of Toronto

Conditions:

Healthy

Eligibility:

FEMALE

18-35 years

Phase:

NA

Brief Summary

In this study, the investigators will use the minimally invasive indicator amino acid oxidation (IAAO) technique to determine protein requirements in weight-trained males. It is hypothesized that the ...

Detailed Description

Provided that energy needs are met, the adequate ingestion of dietary amino acids is the most critical nutritional factor to support the optimal remodeling and deposition of lean body mass in individu...

Eligibility Criteria

Inclusion

  • healthy female weight-trained individuals that have trained consistently for \>1 year
  • complete a physical activity readiness questionnaire (PAR-Q+)
  • Train each muscle group (i.e. chest, back, legs) at least twice a week
  • Meets strength relative to body weight GUIDELINES adapted from Morton et al., 2016; Chilibeck et al., 1997 (sex specific).
  • Bench Press:
  • body weight (kg)\*0.7
  • Leg Press:
  • body weight (kg)\*2.3

Exclusion

  • sedentary for greater than 1 month in the last 6 months prior to the study
  • non-weight stable for the past month
  • smoker
  • Illicit drug use (e.g. growth hormone, testosterone, etc.)
  • Individual plans to increase or decrease body mass in the next 3 months
  • Habitually ingests greater than or equal to 3g protein kg/bw/day
  • Use of supplements such as creatine and beta-alanine in the last 30 days.
  • Hormone-based birth control. Hormonal fluctuations associated with the menstrual cycle have been reported to alter protein metabolism during exercise (Hamadeh, Devries, and Tarnopolsky, 2005) For this reason, the following exclusion criteria will be applied to female participants only: use of birth control and discontinued use within last 3 months
  • Inability to adhere to any of the protocol guidelines

Key Trial Info

Start Date :

November 1 2016

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 30 2018

Estimated Enrollment :

8 Patients enrolled

Trial Details

Trial ID

NCT03397043

Start Date

November 1 2016

End Date

November 30 2018

Last Update

March 29 2019

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