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Clinical Trials/NCT07106489
NCT07106489CompletedNot Applicable

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

Universidad Nacional de Colombia1 site in 1 country10 target enrollmentStarted: February 1, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
Fitness Results From the Bronco Test

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Crossover
Primary Purpose
Other
Masking
Triple (Participant, Care Provider, Investigator)

Masking Description

A person external to the study was tasked with providing a compound to each group and ensuring they were exchanged during the second sample collection, ensuring that both groups received both compounds (the placebo and nitrates) at the end of the study. The professional who performed the physical tests was also blinded throughout the study. Thus, participants knew they would receive a placebo and beetroot, but they were not aware of the order in which they were given the compound.

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Belong to one of the two Rugby Clubs invited to participate
  • Legal age
  • Have trained/played rugby for more than 6 months.

Exclusion Criteria

  • Have had a sports injury in the last 6 months or during the study
  • Use of nutritional supplements during the study.
  • Use of mouthwash during the study.
  • Have health conditions that require specific medical treatment.

Outcomes

Primary Outcomes

Fitness Results From the Bronco Test

Time Frame: First and second physical tests weeks

Fitness is assessed by the time it takes to cover the 1.2 km Bronco test segmented into distances of 20, 40, and 60 meters, which are covered 5 times.

Maximum Strength in the Lower-body Given by Squat

Time Frame: First and second physical tests weeks

Squats are performed technically until reaching 1 repetition maximum (1RM) meeting technical requirements.

Maximum Upper-body Strength Given by Bench Press Test

Time Frame: First and second physical tests weeks

Maximum weight lifted in 1 maximum repetition in a technically correct manner in the bench press exercise

Speed Results Over Distance From 0 to 30 Meters in 40 Meters Sprint Test

Time Frame: First and second physical tests weeks

In the 40-meter speed test, the time taken to travel from the start to the 30 meters is measured in meters per second (m/s)

Maximum Speed Results With the Distance of 30 to 40 Meters in the 40-meter Sprint Test

Time Frame: First and second physical tests weeks

In the 40-meter sprint test, the time to cover from a distance of 30 meters to 40 meters is measured in meters per second (m/s)

Speed Given by Distance From 0 to 40 Meters Sprint

Time Frame: First and second physical tests weeks

Time to cover the distance from 0 to 40 meters sprint at maximum speed in meters per second (m/s)

Results Obtained in the Physical Tests to Evaluate Impact on Acceleration

Time Frame: First and second physical tests weeks

Physical tests are performed over two different weeks. Initially, the 40-meter sprint test is performed with two attempts, with the attempt with the shortest execution time being considered. Distances from 0 to 10 meters are used to evaluate acceleration in meters per second squared (m/s\^2)

Perception of Fatigue Given by the Borg Scale

Time Frame: First and second weeks at the end of the physical tests

According to a score of 1 to 10, with 1 being the lowest and 10 being the highest level of fatigue, participants evaluated their perception at the end of the physical tests.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ligia Stella Guerrero Orjuela

PhD. MSc. ND. Professor

Universidad Nacional de Colombia

Study Sites (1)

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