Impact of Beetroot Supplementation in Athletes

Impact of Beetroot Supplementation on Sports Performance, Prooxidant-antioxidant Balance and Sleep in Athletes

Several previous studies observed a positive effect of beetroot supplementation on sports performance in athletes, mainly in endurance performance. However, less attention has been paid to its effects on short-duration performance, especially in youth athletes. Moreover, only a few previous investigations performed biochemical analyses, including pro-oxidant balance assessments. It is especially important because chronic nitrate intake might directly cause the production of reactive nitrogen species and reactive oxygen species in other subcellular compartments, leading to more oxidative stress. Additionally, no previous study verified the impact of beetroot intake on sleep.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

20

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

      • Kraków, Poland, 31-571
        • University School of Physical Education in Cracow

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:

  • male
  • good general health assessed by physician
  • highly trained
  • written consent to participate

Exclusion Criteria:

  • medication or dietary supplements used within the previous month, which could potentially impact the study outcomes
  • history of sleep nor neurological disorders
  • chronic use (6 months) of any antibacterial mouthwash products.

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Placebo group
Athletes received 7 days of placebo (2 × 70 mL of water with beetroot powder with negligible nitrate content).
Athletes received 7 days of beetroot juice supplementation with nitrate supplementation (2 × 70 mL of beetroot juice ∼12.9 mmol NO3-; Beet It, James White Drinks, Ipswich, UK) or placebo (2 × 70 mL of water with beetroot powder with negligible nitrate content).
Experimental: Beetroot group
Athletes received 7 days of beetroot juice (2 × 70 mL of beetroot juice ∼12.9 mmol NO3-; Beet It, James White Drinks, Ipswich, UK).
Athletes received 7 days of beetroot juice supplementation with nitrate supplementation (2 × 70 mL of beetroot juice ∼12.9 mmol NO3-; Beet It, James White Drinks, Ipswich, UK) or placebo (2 × 70 mL of water with beetroot powder with negligible nitrate content).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Performance test
Time Frame: 7 days after treatment
yo-yo intermittent recovery test level 1
7 days after treatment
Changes in nitrates
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood plasma will be obtained to measure nitrate concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in nitrites
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood plasma will be obtained to measure nitrite concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in prooxidant status
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood plasma will be obtained to measure total oxidative status
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in antioxidant status
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood plasma will be obtained to measure total antioxidant capacity
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in oxidative stress index
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
The oxidative stress index will be calculated as the ratio of plasma prooxidant to antioxidant status
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in nitrooxidative stress markers
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood plasma will be obtained to measure 3-nitrotyrosine concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in protein oxidation
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood plasma will be obtained to measure advanced protein oxidation products concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in nucleic acid oxidation
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood plasma will be obtained to measure ox-8-hydroxy-2'-deoxyguanosine (8-OHdG) concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in lipids oxidation
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood plasma will be obtained to measure thiobarbituric acid reactive substances concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in exercise-induced metabolic acidosis
Time Frame: 1) Before the performance test 2) 3 minutes after the performance test 3) 10 minutes after the performance test 4) 20 minutes after the performance test
Arterialized blood will be obtained to measure lactate concentration
1) Before the performance test 2) 3 minutes after the performance test 3) 10 minutes after the performance test 4) 20 minutes after the performance test
Objective Sleep - Time in bed
Time Frame: nights 1 - 7 during treatment
Total time spent in bed during the night assessed by sleep radar
nights 1 - 7 during treatment
Objective Sleep - Sleep-onset latency
Time Frame: nights 1 - 7 during treatment
The time it takes from when the athlete intends to go to sleep and actually starts to sleep assessed by sleep radar
nights 1 - 7 during treatment
Objective Sleep - Total sleep time
Time Frame: nights 1 - 7 during treatment
Total sleep time obtained from sleep onset to time at wake-up assessed by sleep radar
nights 1 - 7 during treatment
Objective Sleep - Light sleep
Time Frame: nights 1 - 7 during treatment
Total amount of time in light sleep assessed by sleep radar
nights 1 - 7 during treatment
Objective Sleep - Deep sleep
Time Frame: nights 1 - 7 during treatment
Total amount of time in deep sleep assessed by sleep radar
nights 1 - 7 during treatment
Objective Sleep - REM sleep
Time Frame: nights 1 - 7 during treatment
Total amount of time in REM sleep assessed by sleep radar
nights 1 - 7 during treatment
Objective Sleep - Sleep efficiency
Time Frame: nights 1 - 7 during treatment
The percentage of total sleep time to lights off and leaving bed assessed by sleep radar
nights 1 - 7 during treatment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Countermovement jump height
Time Frame: 7 days after treatment
7 days after treatment
Ball speed velocity
Time Frame: 7 days after treatment
7 days after treatment
Sprint test (0-20m)
Time Frame: 7 days after treatment
7 days after treatment
Agility T-test
Time Frame: 7 days after treatment
7 days after treatment
Maximal isometric handgrip strength
Time Frame: 7 days after treatment
7 days after treatment
Flanker task
Time Frame: 7 days after treatment
7 days after treatment
Changes in muscle damage markers
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood serum will be obtained to measure myoglobin concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in muscle enzymes activity
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood serum will be obtained to measure creatine kinase activity
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in inflammation markers
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood serum will be obtained to measure C-reactive protein concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in blood count
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Whole blood will be obtained to measure leukocyte count
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in anabolic hormones
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood serum will be obtained to measure testosterone concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in catabolic hormones
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood serum will be obtained to measure cortisol concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in kidney function markers
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood serum will be obtained to measure creatinine concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in the purine metabolism marker
Time Frame: 1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Blood serum will be obtained to measure uric acid concentration
1) baseline - 2) 7th day of treatment - before the supplementation, 3) 7th day of treatment - before the performance test, 4) 7th day of treatment - immediately after the performance test
Changes in hemoglobin concentration
Time Frame: 1) Before the performance test 2) 3 minutes after the performance test 3) 10 minutes after the performance test 4) 20 minutes after the performance test
Arterialized blood will be obtained to measure hemoglobin concentration
1) Before the performance test 2) 3 minutes after the performance test 3) 10 minutes after the performance test 4) 20 minutes after the performance test
Changes in hematocrit
Time Frame: 1) Before the performance test 2) 3 minutes after the performance test 3) 10 minutes after the performance test 4) 20 minutes after the performance test
Arterialized blood will be obtained to measure hematocrit
1) Before the performance test 2) 3 minutes after the performance test 3) 10 minutes after the performance test 4) 20 minutes after the performance test
Changes in plasma volume
Time Frame: 1) Before the performance test 2) 3 minutes after the performance test 3) 10 minutes after the performance test 4) 20 minutes after the performance test
The change in plasma volume will be calculated using the hemoglobin and hematocrit results
1) Before the performance test 2) 3 minutes after the performance test 3) 10 minutes after the performance test 4) 20 minutes after the performance test

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Aleksandra Filip-Stachnik, Phd, University of Physcial Education in Cracow

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)

August 23, 2023

Primary Completion (Actual)

October 16, 2023

Study Completion (Actual)

October 16, 2023

Study Registration Dates

First Submitted

September 5, 2023

First Submitted That Met QC Criteria

September 14, 2023

First Posted (Actual)

September 21, 2023

Study Record Updates

Last Update Posted (Estimated)

February 1, 2024

Last Update Submitted That Met QC Criteria

January 31, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • AWF_MSIT

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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