Impact of Beetroot Supplementation in Athletes

Sponsor
University School of Physical Education, Krakow, Poland (Other)
Overall Status
Recruiting
CT.gov ID
NCT06043089
Collaborator
University of Bergen (Other)
20
1
2
3.3
6.1

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Beetroot juice supplementation or placebo
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Impact of Beetroot Supplementation on Sports Performance, Prooxidant-antioxidant Balance and Sleep in Athletes
Actual Study Start Date :
Aug 23, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

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).

Dietary Supplement: Beetroot juice supplementation or placebo
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).

Dietary Supplement: Beetroot juice supplementation or placebo
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).

Outcome Measures

Primary Outcome Measures

  1. Performance test [7 days after treatment]

    yo-yo intermittent recovery test level 1

  2. Changes in nitrates [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

  3. Changes in nitrites [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

  4. Changes in prooxidant 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]

    Blood plasma will be obtained to measure total oxidative status

  5. Changes in 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]

    Blood plasma will be obtained to measure total antioxidant capacity

  6. Changes in oxidative stress index [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

  7. Changes in nitrooxidative stress markers [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

  8. Changes in protein oxidation [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

  9. Changes in nucleic acid oxidation [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

  10. Changes in lipids oxidation [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

  11. Changes in exercise-induced metabolic acidosis [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

  12. Objective Sleep - Time in bed [nights 1 - 7 during treatment]

    Total time spent in bed during the night assessed by sleep radar

  13. Objective Sleep - Sleep-onset latency [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

  14. Objective Sleep - Total sleep time [nights 1 - 7 during treatment]

    Total sleep time obtained from sleep onset to time at wake-up assessed by sleep radar

  15. Objective Sleep - Light sleep [nights 1 - 7 during treatment]

    Total amount of time in light sleep assessed by sleep radar

  16. Objective Sleep - Deep sleep [nights 1 - 7 during treatment]

    Total amount of time in deep sleep assessed by sleep radar

  17. Objective Sleep - REM sleep [nights 1 - 7 during treatment]

    Total amount of time in REM sleep assessed by sleep radar

  18. Objective Sleep - Sleep efficiency [nights 1 - 7 during treatment]

    The percentage of total sleep time to lights off and leaving bed assessed by sleep radar

Secondary Outcome Measures

  1. Countermovement jump height [7 days after treatment]

  2. Ball speed velocity [7 days after treatment]

  3. Sprint test (0-20m) [7 days after treatment]

  4. Agility T-test [7 days after treatment]

  5. Maximal isometric handgrip strength [7 days after treatment]

  6. Flanker task [7 days after treatment]

  7. Changes in muscle damage markers [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

  8. Changes in muscle enzymes 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]

    Blood serum will be obtained to measure creatine kinase activity

  9. Changes in inflammation markers [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

  10. Changes in blood 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]

    Whole blood will be obtained to measure leukocyte count

  11. Changes in anabolic hormones [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

  12. Changes in catabolic hormones [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

  13. Changes in kidney function markers [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

  14. Changes in the purine metabolism marker [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

  15. Changes in 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]

    Arterialized blood will be obtained to measure hemoglobin concentration

  16. Changes in 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]

    Arterialized blood will be obtained to measure hematocrit

  17. Changes in plasma volume [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

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 23 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University School of Physical Education in Cracow Kraków Poland 31-571

Sponsors and Collaborators

  • University School of Physical Education, Krakow, Poland
  • University of Bergen

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University School of Physical Education, Krakow, Poland
ClinicalTrials.gov Identifier:
NCT06043089
Other Study ID Numbers:
  • AWF_MSIT
First Posted:
Sep 21, 2023
Last Update Posted:
Sep 21, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Sep 21, 2023