- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05209126
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
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-
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Madrid, Spain, 28223
- Universidad Francisco de Vitoria
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Madrid
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Pozuelo de Alarcón, Madrid, Spain, 28223
- Universidad Francisco de Vitoria
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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:
|
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:
|
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
Keywords
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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