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Search / Trial NCT05422300

A 'Non-Invasive' Breath Test to Determine Anabolic Sensitivity in Females

Launched by UNIVERSITY OF TORONTO · Jun 13, 2022

Trial Information

Current as of June 28, 2025

Recruiting

Keywords

Dietary Proteins/Administration & Dosage Skeletal Muscle Metabolism Human Adult Females Diet Exercise; Resistance Exercise Amino Acids Muscle Protein Synthesis Skeletal Muscle Anabolism Stable Isotopes

ClinConnect Summary

This clinical trial is studying a new, non-invasive breath test designed to measure how well young women use protein from their food to build muscle. Maintaining lean body mass, especially muscle, is important for overall health. The researchers want to see if this breath test, which has been tested in men, is effective in women as well. The goal is to find out whether different groups of women are sensitive to dietary protein and how this affects their ability to gain or lose muscle mass.

To participate, women aged 18 to 35 who are physically active at least once a week and have a body mass index (BMI) within a certain range can apply. Participants need to have regular menstrual cycles and should not be using hormonal contraceptives or certain medications that could affect protein metabolism. During the trial, participants will perform exercise and provide breath samples, which will help researchers understand their protein processing better. This study is a great opportunity for eligible women to contribute to important research that could lead to better health recommendations in the future.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Female sex
  • 18-35 years of age
  • BMI ≥18.5 kg/m2 and ≤ 30 kg/m2
  • Eumenorrheic (self-reported menstruation for prior 3 consecutive months)
  • Recreationally active; currently performing structured exercise (e.g. running, weightlifting, team-sport activity) at least once per week for ≥ 6 months before enrolment
  • Exclusion Criteria:
  • Use of oral contraceptives
  • Inability to perform physical activity as determined by the PAR-Q+
  • Inability to adhere to protocol guidelines (e.g. alcohol, caffeine, habitual diet)
  • Regular tobacco use
  • Illicit drug use (e.g. growth hormone, testosterone, etc...)
  • Diagnosed medical condition under the care of a physician (e.g. type 2 diabetes)
  • Inability to abstain from supplements (e.g. protein, creatine, HMB, BCAA, phosphatidic acid, etc...) at least three weeks before the trial
  • Individuals on any medications known to affect protein metabolism (e.g. corticosteroids, non-steroidal anti-inflammatories, and/or prescription-strength acne medications)

About University Of Toronto

The University of Toronto, a prestigious research institution, serves as a leading sponsor of clinical trials dedicated to advancing medical knowledge and improving patient care. With a commitment to innovation and excellence, the university fosters a collaborative environment that brings together multidisciplinary teams of experts in medicine, pharmacology, and public health. Through rigorous research methodologies and ethical standards, the University of Toronto aims to explore new therapies, assess treatment efficacy, and address critical health challenges, ultimately contributing to the global body of scientific knowledge and enhancing healthcare outcomes.

Locations

Toronto, Ontario, Canada

Patients applied

0 patients applied

Trial Officials

Nicki Pourhashemi, MSc Student

Study Director

Faculty of Kinesiology and Physical Education

Hugo JW Fung, PhD (c)

Study Director

Faculty of Kinesiology and Physical Education

Jonathan Aguilera, PhD Student

Study Director

Faculty of Kinesiology and Physical Education

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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