- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06043089
Impact of Beetroot Supplementation in Athletes
January 31, 2024 updated by: University School of Physical Education, Krakow, Poland
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
Intervention / Treatment
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
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Kraków, Poland, 31-571
- University School of Physical Education in Cracow
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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
- 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 |
|---|---|
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Placebo Comparator: Placebo group
Athletes received 7 days of placebo (2 × 70 mL of water with beetroot powder with negligible nitrate content).
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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).
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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).
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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).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Performance test
Time Frame: 7 days after treatment
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yo-yo intermittent recovery test level 1
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7 days after treatment
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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
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Blood plasma will be obtained to measure nitrate concentration
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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
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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
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Blood plasma will be obtained to measure nitrite concentration
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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
|
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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
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Blood plasma will be obtained to measure total oxidative status
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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
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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
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Blood plasma will be obtained to measure total antioxidant capacity
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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
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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
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The oxidative stress index will be calculated as the ratio of plasma prooxidant to antioxidant status
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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
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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
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Blood plasma will be obtained to measure 3-nitrotyrosine concentration
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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
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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
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Blood plasma will be obtained to measure advanced protein oxidation products concentration
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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
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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
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Blood plasma will be obtained to measure ox-8-hydroxy-2'-deoxyguanosine (8-OHdG) concentration
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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
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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
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Blood plasma will be obtained to measure thiobarbituric acid reactive substances concentration
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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
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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
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Arterialized blood will be obtained to measure lactate concentration
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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
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Objective Sleep - Time in bed
Time Frame: nights 1 - 7 during treatment
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Total time spent in bed during the night assessed by sleep radar
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nights 1 - 7 during treatment
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Objective Sleep - Sleep-onset latency
Time Frame: nights 1 - 7 during treatment
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The time it takes from when the athlete intends to go to sleep and actually starts to sleep assessed by sleep radar
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nights 1 - 7 during treatment
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Objective Sleep - Total sleep time
Time Frame: nights 1 - 7 during treatment
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Total sleep time obtained from sleep onset to time at wake-up assessed by sleep radar
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nights 1 - 7 during treatment
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Objective Sleep - Light sleep
Time Frame: nights 1 - 7 during treatment
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Total amount of time in light sleep assessed by sleep radar
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nights 1 - 7 during treatment
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Objective Sleep - Deep sleep
Time Frame: nights 1 - 7 during treatment
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Total amount of time in deep sleep assessed by sleep radar
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nights 1 - 7 during treatment
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Objective Sleep - REM sleep
Time Frame: nights 1 - 7 during treatment
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Total amount of time in REM sleep assessed by sleep radar
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nights 1 - 7 during treatment
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Objective Sleep - Sleep efficiency
Time Frame: nights 1 - 7 during treatment
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The percentage of total sleep time to lights off and leaving bed assessed by sleep radar
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nights 1 - 7 during treatment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Countermovement jump height
Time Frame: 7 days after treatment
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7 days after treatment
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Ball speed velocity
Time Frame: 7 days after treatment
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7 days after treatment
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Sprint test (0-20m)
Time Frame: 7 days after treatment
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7 days after treatment
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Agility T-test
Time Frame: 7 days after treatment
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7 days after treatment
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Maximal isometric handgrip strength
Time Frame: 7 days after treatment
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7 days after treatment
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Flanker task
Time Frame: 7 days after treatment
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7 days after treatment
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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
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Blood serum will be obtained to measure myoglobin concentration
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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
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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
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Blood serum will be obtained to measure creatine kinase activity
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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
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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
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Blood serum will be obtained to measure C-reactive protein concentration
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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
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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
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Whole blood will be obtained to measure leukocyte count
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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
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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
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Blood serum will be obtained to measure testosterone concentration
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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
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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
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Blood serum will be obtained to measure cortisol concentration
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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
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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
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Blood serum will be obtained to measure creatinine concentration
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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
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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
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Blood serum will be obtained to measure uric acid concentration
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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
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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
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Arterialized blood will be obtained to measure hemoglobin concentration
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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
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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
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Arterialized blood will be obtained to measure hematocrit
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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
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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
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The change in plasma volume will be calculated using the hemoglobin and hematocrit results
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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
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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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