Impact of Beetroot Juice Ingestion on Female Rugby Performance (BEETJUICERUGBY)

April 20, 2022 updated by: Universidad Francisco de Vitoria

Impact of an Acute Beetroot Ingestion on Neuromuscular Performance in Female Rugby Players

Rugby is a team sport characterized by high-intermittent efforts, due to the importance of realizing intermittent and explosive efforts in rugby the use of nutritional strategies such as beetroot ingestion should be explored with the aim to enhance the capacity for repeating high-intensity actions in female players.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Rugby is a team sport characterized by high-intermittent efforts, thus, to the importance of realizing intermittent and explosive efforts in field hockey is crucial. For this reason, the use of nutritional strategies in field hockey should be explored with the aim to enhance the capacity for repeating high-intensity actions. However, scientific evidence supports only a few numbers of dietary supplements that have reported good evidence for improving sports performance, between we can mention beetroot juice supplementation with doses > 5 mmol of NO3-. Beetroot juice is a NO3- precursor with recognized effectiveness to elicit performance due to different physiological mechanisms associated with its ingestion such as increment in vasodilatation, skeletal muscle contractility, or delaying fatigue development that could be linked with an enhance or performance in team-sports athletes. However, the majority of the studies has been realized in male athletes being female athletes underrepresented in beetroot juice supplementation research. Thus, the aim of this study was to analyze the effects of beetroot juice ingestion on neuromuscular performance in female rugby players.

Study Type

Interventional

Enrollment (Actual)

13

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, 28223
        • Universidad Francisco de Vitoria
    • Madrid
      • Pozuelo de Alarcón, Madrid, Spain, 28223
        • Universidad Francisco de Vitoria

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

18 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • More than 5 years of rugby training experience.
  • Active rugby player

Exclusion Criteria:

  • Concurrently participating in other studies.
  • Contraindications to beetroot juice ingestion.
  • Physical limitations, health problems, or musculoskeletal injuries.

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 supplementation
One serving 140 mL of beetroot juice (12.8 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) 3 h before initiating the testing session.
Acute effects of beetroot juice ingestion on neuromuscular performance in female rugby players
Other Names:
  • Nitrate precursors
Placebo Comparator: Placebo supplementation
One serving 140 mL of beetroot juice placebo (0.08 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) 3 h before initiating the testing session.
Acute effects of beetroot juice ingestion on neuromuscular performance in female rugby players
Other Names:
  • Nitrate precursors

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Bronco Aerobic Fitness Test
Time Frame: 1-week
Time to complete test using photocell timing gates
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
Changes in maximal isometric handgrip strength (kg)
Time Frame: 1-week
Using a hand-held dynamometer
1-week
Changes in 30-meters sprint time (s)
Time Frame: 1 week
Time to complete 30-m sprints using photocell timing gates
1 week
Changes in rate of perceived exertion scale
Time Frame: 1-week
Differences between placebo and beetroot juice in rate of perception exertion scale
1-week
Changes in side effects questionnarie
Time Frame: 1-week
Differences between placebo and beetroot juice in side effects health aspects
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)

January 20, 2022

Primary Completion (Actual)

January 27, 2022

Study Completion (Actual)

January 30, 2022

Study Registration Dates

First Submitted

January 14, 2022

First Submitted That Met QC Criteria

January 14, 2022

First Posted (Actual)

January 26, 2022

Study Record Updates

Last Update Posted (Actual)

April 21, 2022

Last Update Submitted That Met QC Criteria

April 20, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • Universidad_FranciscoVitoria

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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