- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05209139
Beetroot Juice Ingestion Effects on Field Hockey Performance. (BEETHOCKEY)
April 13, 2022 updated by: Universidad Francisco de Vitoria
Acute Effects of Beetroot Juice Ingestion on Neuromuscular Performance and Match-play Demands in Elite Female Hockey Players.
Scientific evidence supports that only a few dietary supplements have reported good evidence for improving sports performance, between we can mention beetroot juice supplementation with doses > 5 mmol of NO3-.
In this randomized placebo-controlled study, we investigated the effects of BJ acute supplementation in improving neuromuscular performance and match-play demands in female field hockey players.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Beetroot juice supplementation has demonstrated good evidence for improving sports performance, however, benefits in team sports, especially in female athletes, are underrepresented.
In this randomized placebo-controlled study, we investigated the effects of beetroot juice acute supplementation in improving neuromuscular performance and match-play demands.Testing sessions will comprise a neuromuscular test battery consisting of a countermovement jump (CMJ), isometric handgrip strength, 20-m sprint and repeated sprint ability test, followed by a 20-minute simulated field hockey Physical match activity (distances, speeds, accelerations and decelerations) will be monitored in real-time using an inertial tracking system
Study Type
Interventional
Enrollment (Actual)
11
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
-
-
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 35 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Elite female field hockey players (playing in First Field Hockey Division).
- More than 8 years of field hockey training experience.
Exclusion Criteria:
- Concurrently participating in other studies.
- Contraindications associated to beetroot ingestion.
- Health problems or musculoskeletal injuries 6 months previous to study realization
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
Acute beetroot juice supplementation
|
One serving 70 mL of beetroot juice (6.4 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) 3 h before initiating the testing session.
One serving 70 mL of beetroot juice placebo (0.04 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) 3 h before initiating the testing session.
|
Placebo Comparator: Placebo supplementation
Acute placebo supplementation
|
One serving 70 mL of beetroot juice (6.4 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) 3 h before initiating the testing session.
One serving 70 mL of beetroot juice placebo (0.04 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) 3 h before initiating the testing session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes in simulated field hockey match demands (m/min)
Time Frame: 1 week
|
Using a global position system (GPS)
|
1 week
|
Changes in repeated-sprint-ability test (s)
Time Frame: 1 week
|
Time to complete the modified repeated sprint ability test using photocell timing gates
|
1 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes in sprint time (s)
Time Frame: 1 week
|
Time to complete 20-m sprints using photocell timing gates
|
1 week
|
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 (N)
Time Frame: 1 week
|
Using a hand-held dynamometer
|
1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)
March 1, 2018
Primary Completion (Actual)
March 8, 2018
Study Completion (Actual)
March 15, 2018
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 14, 2022
Last Update Submitted That Met QC Criteria
April 13, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- Universidad Francisco_Vitoria
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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