- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05422300
A 'Non-Invasive' Breath Test to Determine Anabolic Sensitivity in Females (FBT)
The maintenance of lean body mass, especially skeletal muscle, is vital for optimal health and performance across the lifespan. The protein component of lean body mass is in a constant state of turnover, involving the simultaneous breakdown of old and/or damaged proteins and the synthesis of new proteins. These processes collectively determine if someone gains or loses lean body mass. Eating a protein-rich meal or performing resistance exercise can stimulate protein synthesis to gain lean body mass. Stable isotope "tracers" are amino acid building blocks that are slightly heavier than those naturally found in the body. In research, these are often used to assess changes in protein turnover in response to feeding and/or exercise. However, traditional stable isotope tracer methods involve the intravenous delivery of a tracer with blood sampling and muscle biopsies, which may be cumbersome or unfeasible for some for participants.
The investigators have recently developed and validated a non-invasive 'breath test' in males that measures the efficiency of the body for using amino acids in food to build new body proteins. The principle of this method is that leucine, an essential amino acid that the body must acquire from normal diet, can be used to build new body proteins or as a source of energy (i.e., oxidized). Since leucine is preferentially used in skeletal muscle, skeletal muscle protein metabolism can be non-invasively inferred . Any leucine "tracer" that is oxidized can be detected and measured in the carbon dioxide exhaled. It has been observed that less dietary leucine is oxidized when active males perform a bout of resistance exercise, meaning more was used to build muscle proteins. When performed habitually, resistance exercise can help skeletal muscles grow, compared to a rested-state, resulting in greater leucine retention in the body to build new proteins. Therefore, the purpose of this study is to validate this non-invasive breath test in females to increase the validity of the method in a wider range of populations. Ultimately, the results will further validate this non-invasive tool that can potentially detect whether different populations are sensitive to dietary amino acids and in a position to gain or lose lean body mass.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Daniel R Moore, PhD
- Phone Number: 4169464088
- Email: dr.moore@utoronto.ca
Study Contact Backup
- Name: Michael Mazzulla, PhD
- Email: m.mazzulla@mail.utoronto.ca
Study Locations
-
-
Ontario
-
Toronto, Ontario, Canada, M5S 2C9
- Recruiting
- University of Toronto
-
Contact:
- Nicki Pourhashemi, MSc Student
-
Contact:
- Daniel R Moore, PhD
- Phone Number: 416-946-4088
- Email: dr.moore@utoronto.ca
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
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)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mid-Follicular Phase
7-10 days after the onset of menses, determined by self-reports and confirmed with ovulation test kits.
|
Subjects will be fed a mixed-macronutrient beverage at rest (0.75g/kg lean body mass of carbohydrates; 0.25g/kg lean body mass of protein).
Amino acid composition of the protein will be modelled off the composition of egg.
Leucine content will be enriched to 5% with [13C]-leucine.
Other Names:
Participants will be subjected to a full-body resistance exercise protocol, consisting of an upper and lower body circuit. The upper body circuit will be a chest press and dumbbell row superset, whereas the lower body circuit will be leg press and leg extension (4 sets of 10 repetitions @ 75% of their 1 repetition max, respectively). The inter-set rest period will be 90 seconds. Subjects will be fed a mixed-macronutrient beverage at rest (0.75g/kg lean body mass of carbohydrates; 0.25g/kg lean body mass of protein). Amino acid composition of the protein will be modelled off the composition of egg. Leucine content will be enriched to 5% with [13C]-leucine.
Other Names:
|
|
Experimental: Mid-Luteal Phase
5-7 days after ovulation, determined by self-reports and confirmed with ovulation test kits.
|
Subjects will be fed a mixed-macronutrient beverage at rest (0.75g/kg lean body mass of carbohydrates; 0.25g/kg lean body mass of protein).
Amino acid composition of the protein will be modelled off the composition of egg.
Leucine content will be enriched to 5% with [13C]-leucine.
Other Names:
Participants will be subjected to a full-body resistance exercise protocol, consisting of an upper and lower body circuit. The upper body circuit will be a chest press and dumbbell row superset, whereas the lower body circuit will be leg press and leg extension (4 sets of 10 repetitions @ 75% of their 1 repetition max, respectively). The inter-set rest period will be 90 seconds. Subjects will be fed a mixed-macronutrient beverage at rest (0.75g/kg lean body mass of carbohydrates; 0.25g/kg lean body mass of protein). Amino acid composition of the protein will be modelled off the composition of egg. Leucine content will be enriched to 5% with [13C]-leucine.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exogenous Leucine Oxidation (umol/kg)
Time Frame: 6 hours
|
Exogenous Leucine Oxidation determined from breath 13CCO2 enrichment.
Breath samples will be collected every 20-30min after test drink ingestion to determine breath 13CO2 enrichment.
Total leucine oxidation will be determined from the area under the 13CO2 enrichment by time curve.
|
6 hours
|
|
Net-Leucine Retention (umol/kg)
Time Frame: 6 hours
|
Whole-Body Net Leucine Retention determined from the difference between exogenous leucine oxidation and leucine ingestion the 6 hour measurement period.
|
6 hours
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Nicki Pourhashemi, MSc Student, Faculty of Kinesiology and Physical Education
- Study Director: Hugo JW Fung, PhD (c), Faculty of Kinesiology and Physical Education
- Study Director: Jonathan Aguilera, PhD Student, Faculty of Kinesiology and Physical Education
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FBT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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