Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date January 2020
Source University of Manitoba
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Beet It Sport Shot
Commercially available concentrated beetroot juice supplement intended for athletes.
Other:
Placebo
Fruit juice cordial containing negligible nitrate

Locations

Country Name City State
Canada Richardson Centre for Functional Foods and Nutraceuticals Winnipeg Manitoba

Sponsors (1)

Lead Sponsor Collaborator
University of Manitoba

Country where clinical trial is conducted

Canada, 

Outcome

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
See also
  Status Clinical Trial Phase
Completed NCT05518214 - 'Oral Microbiome -Dietary Nitrate' Interactions and Cognitive Health in Older Age N/A
Completed NCT04859491 - Effect of Carbohydrate-protein Co-ingestion on Short-term Recovery N/A