Acute Effects of Beetroot Juice Ingestion on Cognitive Function and Neuromuscular Performance in Elite Female Taekwondo Athletes (BEET_TAEKWONDO)

November 4, 2024 updated by: Universidad Pontificia Comillas
Beetroot juice is a good source of nitrate (NO3-), which is a precursor of nitric oxide (NO) through the NO3- to nitrite (NO2-) to NO pathway (Lundberg et al., 2008). Consequently, it is thought that a minimum threshold may exist for dietary NO3- consumption of at least 5 mmol to enhance athletic performance (Senefeld et al., 2020). In turn, systematic reviews have documented that the use of beetroot juice supplementation enhances muscle strength and power-related attributes (Gonzalez et al., 2023), as well as performance in repeated high-intensity activity bouts (Alsharif et al., 2023; Dominguez et al., 2018). However, beetroot juice supplementation has been shown to have equivocal effects on neuromuscular performance specifically among individual sport athletes (e.g. taekwondo). Thus, the aim of this study was to determine the effects of acute beetroot juice ingestion (140 mL, 12.8 mmol NO3-) on neuromuscular performance in elite female taekwondo athletes.

Study Overview

Detailed Description

Beetroot juice is a good source of nitrate (NO3-), which is a precursor of nitric oxide (NO) through the NO3- to nitrite (NO2-) to NO pathway (Lundberg et al., 2008). This pathway is thought to promote increased sarcoplasmic reticulum calcium release and re-uptake with ensuing enhancements in force output within type II muscle fibers (Hernandez et al., 2012), as well as increased neurotransmitter release (Esen et al., 2022) and attenuated muscle potassium efflux (Wylie et al., 2013) that could benefit neuromuscular performance. Consequently, it is thought that a minimum threshold may exist for dietary NO3- consumption of at least 5 mmol to enhance athletic performance (Senefeld et al., 2020). In turn, systematic reviews have documented that the use of beetroot juice supplementation enhances muscle strength and power-related attributes (Gonzalez et al., 2023), as well as performance in repeated high-intensity activity bouts (Alsharif et al., 2023; Dominguez et al., 2018). However, beetroot juice supplementation has been shown to have equivocal effects on neuromuscular performance specifically among individual sport athletes (e.g. taekwondo). Thus, the aim of this study was to determine the effects of acute beetroot juice ingestion (140 mL, 12.8 mmol NO3-) on neuromuscular performance in elite female taekwondo athletes.

Study Type

Interventional

Enrollment (Actual)

7

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Madrid, Spain
        • Universida Pontificia Comillas

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age between 16 to 40 years
  • Competed in international taekwondo competitions representing her national teams.
  • More than6 years of training experience (at least 3 sessions per week).
  • Female taekwondo athletes.

Exclusion Criteria:

  • Male taekwondo athletes.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Beetroot juice supplementation
140 mL of beetroot juice (12.8 mmol of NO3-, Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) made from concentrates of beetroot juice (98%) and lemon juice (2%) (nutritional information (per 100 mL), energy: 373 kJ; fat: 0 g; carbohydrates: 18 g [sugars: 17 g]; protein: 3.7 g; salt: 0.48 g)
One serving 140 mL of BJ (12.8 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) after an overnight fast and 2.5 h before initiating the testing session.
Placebo Comparator: Placebo supplementation
140 mL of beetroot juice placebo without nitrates (0.08 mmol of NO3-, Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) made from concentrates of beetroot juice (98%) and lemon juice (2%) (nutritional information (per 100 mL), energy: 373 kJ; fat: 0 g; carbohydrates: 18 g [sugars: 17 g]; protein: 3.7 g; salt: 0.48 g)
One serving 140 mL of BJ (0.04 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) after an overnight fast and 2.5 h before initiating the testing session.
Other Names:
  • Beetroot juice placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Simulated taekwondo Combat (actions/time)
Time Frame: 1-week
Simulated taekwondo combat were performed according to the guidelines of the World Taekwondo (WT), and participants were divided based in the Olympic weight categories (WT, 2016). All the combats were executed in an official octagonal and homologated competition area while an international referee (who doesn´t know the experimental treatments) arbitrated. Today the rules of WTF led to use electronic protectors as protecting of athletes and identify electronically the punctuations (Del Vecchio, Franchini, Del Vecchio, & Pieter, 2011). Variables analyzed were attack time (AT), step time (ST), pause time (PT), period without attack (PWA = ST+PT), numbers of attacks (AN), the ratio for attack time and step time (R1 = AT/ST), and ratio for action time and step time (R2 = (AT+ST) /PT).
1-week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in maximal jump height (cm)
Time Frame: 1-week
Maximal jump height using a contact platform
1-week
Reaction time (ms)
Time Frame: 1-week
Reaction times in a specific reaction test with BlazePod ((Play Coyotta Ltd., Tel Aviv, Israel)
1-week
Blood lactate concentrations (mmol·L-1)
Time Frame: 1-week
Previous to the warm-up, just to the end of the simulated combat, and 3 minutes after, a researcher extracted a blood sample of the pad of the index finger of the left hand of the participants.
1-week
Rating of percevied exertion (RPE) (measured using scale 6-20 points)
Time Frame: 1-week
Immediately after each one of the 3 assaults, participants were asked for providing her RPE using a Borg scale from 6 to 20 points
1-week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2022

Primary Completion (Actual)

July 1, 2022

Study Completion (Actual)

August 15, 2022

Study Registration Dates

First Submitted

November 4, 2024

First Submitted That Met QC Criteria

November 4, 2024

First Posted (Estimated)

November 5, 2024

Study Record Updates

Last Update Posted (Estimated)

November 5, 2024

Last Update Submitted That Met QC Criteria

November 4, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Ethics Committee: 22/172-E_TFM

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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