Clinical Trials Directory

Trials / Completed

CompletedNCT07106489

Effect of Beetroot Nitrates on Different Physical Skills in Colombian Rugby Athletes

Effect of Beetroot Extract Supplementation on the Athletic Performance of Trained Rugby Athletes

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Universidad Nacional de Colombia · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Beetroot is a source of nitrates, which have demonstrated various positive effects in sports, with little evidence in intermittent sports such as ball sports (including rugby). Therefore, the study's hypothesis is that it may also have an effect in these sports. For this purpose, a beetroot extract was used, a product approved by the Colombian institution in charge of product approval and registration in Colombia, the National Institute for Food and Drug Surveillance (INVIMA). This was done to determine whether it has any effect on various physical abilities required for rugby, such as speed, acceleration, strength, and fatigue perception.

Detailed description

Currently, nitrates (from beet juices or extracts) have gained relevance due to their vasodilatory effect, which has contributed to improving athletic performance. Their use has been studied mainly in continuous sports such as swimming, cycling, athletics, etc. However, research in intermittent sports (such as ball or combat sports) is limited and inconclusive, so further research is needed on their use and effect in these sports. Therefore, the study seeks to investigate the effect of administering beet extract for three consecutive days in rugby athletes, evaluating its effect on various physical capacities required for the specific sport, such as acceleration, speed, strength, and fitness. Due to the small number of participants, a randomization process is not possible. A representative sample of 44 is required, but only 10 are interested in participating. Therefore, the sample will be selected based on the number of people willing to participate (convenience sampling) and meeting the defined inclusion and exclusion criteria. Each athlete is subsequently characterized and evaluated by the nutritionist, who provides instructions on how to avoid consuming foods or substances that could affect the study. They will be provided with the necessary substrates three days before the physical tests, with one group receiving the beetroot substrate and the other a placebo. The following week, the groups will be double-blinded. The physical tests will be performed by a professional physiotherapist, who will apply the test protocol and use a Borg scale to assess perceived exertion. Finally, a descriptive and exploratory analysis will be performed on the collected data, using univariate tests for the mean (Student's t-test) or Wilcoxon tests, depending on the type of variable (continuous or ordinal), with a 95% confidence level. To measure the magnitude of the treatment effect on each measured variable, Cohen's d statistic will be used for those variables that required a t-test.

Conditions

Interventions

TypeNameDescription
OTHERbeetroot juice - PlaceboParticipants receive the beetroot and placebo in the form of waffles to ensure the study is blinded, as the 6 mmol of nitrates used require a high concentration of beetroot, which is masked by the waffle ingredients and food coloring.
OTHER40 meters sprintThe participant performs a race at maximum speed with two attempts, times are taken at 10, 30 and 40 meters, to evaluate acceleration and speed, the attempt with the shortest times is the one taken for the research.
OTHERFitness test by bronco testThe participant runs a distance of 20, 40, and 60 meters, back and forth, 5 times at maximum speed. The variable to be measured is the total time taken to complete the test.
OTHERMaximal strengthEach participant performs squats and bench press to evaluate lower-body and upper-body maximal strength, thus identifying their maximum strength taken per kilogram lifted.
OTHERBorg scaleAt the end of the tests, each participant is asked to evaluate their perception of fatigue by giving a number between 1 and 10, with 1 being the lowest level of fatigue and 10 being the highest.

Timeline

Start date
2025-02-01
Primary completion
2025-03-05
Completion
2025-03-13
First posted
2025-08-06
Last updated
2025-12-12
Results posted
2025-12-12

Locations

1 site across 1 country: Colombia

Source: ClinicalTrials.gov record NCT07106489. Inclusion in this directory is not an endorsement.