Anaerobic Exercise Clinical Trial
Official title:
Evaluation of Various Doses of Beetroot Juice on Anaerobic Performance
NCT number | NCT02919254 |
Other study ID # | J2015:108 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | August 2016 |
Est. completion date | December 2018 |
Verified date | January 2020 |
Source | University of Manitoba |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to examine the effect of varying nitrate doses of beetroot juice supplementation on dynamic, multijoint resistance exercise performance in active, trained individuals. Performance will be assessed based on parameters including neuromuscular efficiency, anaerobic performance capability, oxygen consumption, plasma nitrate/nitrite levels, specific muscle tissue biomarkers including lactate, and anthropometric measurements of select muscle groups.
Status | Completed |
Enrollment | 13 |
Est. completion date | December 2018 |
Est. primary completion date | May 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 35 Years |
Eligibility |
Inclusion Criteria: - Minimum 6 consecutive months experience in resistance training, engaging at least 2 times per week. - Possess sufficient mobility to properly execute movements required in testing protocol Exclusion Criteria: - Usage of any banned dietary supplements or performance enhancing drugs (thermogenics, anabolic steroids, prohormones, etc.) - Any physical condition or malady that would impede participant from performing exercise or by doing so, endanger the individual |
Country | Name | City | State |
---|---|---|---|
Canada | Richardson Centre for Functional Foods and Nutraceuticals | Winnipeg | Manitoba |
Lead Sponsor | Collaborator |
---|---|
University of Manitoba |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Muscle activation and fiber recruitment | Muscle activation/fiber recruitment to be measured in millivolts (mV) using electromyography (EMG) sensor during maximum voluntary contractions (MVC) and compared between study arms. | 5 weeks | |
Secondary | Plasma nitrate/nitrite levels | Plasma nitrate and nitrite levels will be measured at baseline and after 7 days of supplementation and compared between study arms. | 5 weeks | |
Secondary | Number of repetitions performed | Total number of repetitions in each session and number of repetitions performed at each respective % of 1 repetition maximum during each session will be recorded and compared between study arms. | 5 weeks | |
Secondary | Oxygen consumption | Total oxygen consumption during testing sessions will be recorded and compared between study arms. | 5 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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