- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06675305
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
Status
Completed
Conditions
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:
|
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.
Sponsor
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
Keywords
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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