- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04210531
Beetroot Juice Supplementation in Basketball Players
December 20, 2019 updated by: Javier Courel Ibáñez, Universidad de Murcia
Effects of Beetroot Juice Supplementation in Neuromuscular Performance and Match Activity in Young Basketball Players
Whereas beetroot juice (BJ) supplementation is shown to increase physical performance in endurance activities, its benefits in team sports has been barely studied.
In this randomized placebo-controlled study, we investigated the effects of BJ acute supplementation in improving neuromuscular performance and physical match activity in basketball.
Study Overview
Status
Completed
Conditions
Detailed Description
Whereas beetroot juice (BJ) supplementation is shown to increase physical performance in endurance activities, its benefits in team sports has been barely studied.
In this randomized placebo-controlled study, we investigated the effects of BJ acute supplementation in improving neuromuscular performance and physical match activity in basketball.Testing sessions will comprised a neuromuscular test battery consisting of a countermovement jump (CMJ), isometric handgrip strength, 10-m/20-m sprint and agility T-test, followed by a 40-minute simulated basketball match.
Physical match activity (distances, speeds, accelerations and decelerations) will be monitored in real time using an inertial tracking system
Study Type
Interventional
Enrollment (Actual)
10
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
-
-
San Javier
-
Murcia, San Javier, Spain, 30720
- Faculty of Sport Sciences
-
-
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
15 years to 16 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- active basketball player
- more than 5 years of basketball training experience
Exclusion Criteria:
- concurrently participating in other studies
- contraindications to BJ diet
- 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: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: BJ supplementation
Acute beetroot juice (BJ) supplementation
|
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 3 h before initiating the testing session.
|
|
Placebo Comparator: PLA supplementation
Acute placebo (PLA) supplementation
|
One serving placebo drink (0.08 mmol of NO3-; Salud Viva, Nano Salud 32 S.L) after an overnight fast and 3 h before initiating the testing session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in baskeball 5-on-5 game activity (m/min)
Time Frame: 1 week
|
Using a wireless inertial movement unit system
|
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 dynamometer
|
1 week
|
|
Changes in sprint time (s)
Time Frame: 1 week
|
Time to complete 10-m and 20-m sprints using photocell timing gates
|
1 week
|
|
Changes in agility test (s)
Time Frame: 1 week
|
Time to complete the modified T-test using photocell timing gates
|
1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
June 9, 2019
Primary Completion (Actual)
June 12, 2019
Study Completion (Actual)
June 12, 2019
Study Registration Dates
First Submitted
December 19, 2019
First Submitted That Met QC Criteria
December 20, 2019
First Posted (Actual)
December 24, 2019
Study Record Updates
Last Update Posted (Actual)
December 24, 2019
Last Update Submitted That Met QC Criteria
December 20, 2019
Last Verified
December 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 2421/2019
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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