Effect of the Beetroot Juice in Portuguese Swimmers

Sponsor
Universidad Francisco de Vitoria (Other)
Overall Status
Completed
CT.gov ID
NCT05657093
Collaborator
Universidad Politécnica de Madrid. (Other), Instituto Politécnico de Bragança (Other)
18
1
2
7
78.3

Study Details

Study Description

Brief Summary

Objective: To investigate whether an acute intake of beet juice (BJ) improved the factors of total and split times (performance), stroke frequency and CMJ (biomechanics), lactate and HR (physiology) and RPE-TQR (psychophysiological) in a repeated (performance), stroke frequency and CMJ (biomechanics), lactate and HR (physiology) and RPE-TQR (psychophysiological) in a repeated maximal speed swimming effort in elite swimmers.

Methods: A total of 18 elite swimmers participated in this randomized, double-blind study. In 2 different trials, swimmers ingested a Beet-It injection (70 ml placebo (PL) or a Beet-It injection of 70 ml beet juice (BJ)) 3 hours before undergoing a 2x6x100 m intermittent maximal speed crawl performance test.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Beetroot Juice
  • Combination Product: Placebo
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
18 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Parallel allocation was carried out in the two groupsParallel allocation was carried out in the two groups
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Masking Description:
Triple blinded (Participant, Investigator and Outcomes Assessor) The participant was blinded not knowing the treatment to which he was submitted, investigator and outcome assessor responsible for collecting the results, without commenting on the group from which the subject came.
Primary Purpose:
Treatment
Official Title:
"Effects of Beetroot Juice os Sport Performane in Elite Swimmers. A Randomized Clinical Trial"
Actual Study Start Date :
Apr 30, 2022
Actual Primary Completion Date :
May 7, 2022
Actual Study Completion Date :
May 7, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Beetroot juice

The swimmers ingested a shot of Beet-It 70 ml beetroot juice (BJ)) 3 hours before undergoing a 2x6x100m crawl intermittent maximal speed performance test.

Dietary Supplement: Beetroot Juice
The swimmers drank 3 hours before the test, mL70 of BJ (containing mmol6.4 of NO-3) (Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) or PLA (0.04 mmol of NO-3)

Combination Product: Placebo
The swimmers drank 3 hours before the test, mL70 of BJ (containing mmol6.4 of NO-3) (Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) or PLA (0.04 mmol of NO-3)

Placebo Comparator: Placebo

The swimmers ingested a shot of Beet-It (70 ml placebo (PL)) 3 hours before undergoing a 2x6x100m crawl intermittent maximal speed performance test.

Dietary Supplement: Beetroot Juice
The swimmers drank 3 hours before the test, mL70 of BJ (containing mmol6.4 of NO-3) (Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) or PLA (0.04 mmol of NO-3)

Combination Product: Placebo
The swimmers drank 3 hours before the test, mL70 of BJ (containing mmol6.4 of NO-3) (Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) or PLA (0.04 mmol of NO-3)

Outcome Measures

Primary Outcome Measures

  1. Lactate concentration [3 hours post-dose of Beetroot juice or Placebo]

    After qeach even series of 100m (2nd, 4th, 6th and 3' rest), their finger was wiped dry and their blood lactate concentration was measured with a Lactate Pro2 portable analyzer 1 minute after completing each 100m series.

  2. Rate of Perceived Exertion [3 hours after ingestion of the beetroot juice]

    During every 100m, they were asked how much effort they had exerted using the subjective RPE scale as in other studies with BJ and swimming.

  3. Recovery Total Quality Scale [3 hours after ingestion of the beetroot juice]

    Before the swimmers performed the next 100m, they were asked how recovered they felt, using another subjective TQR scale.

  4. Total Time [3 hours after ingestion of the beetroot juice]

    The complete 2x6x100 main test was recorded with a JVC model GY-HM150E video camera placed on the stand of the facility itself at about 10 m from the start/turn wall (approximately 5 m above and 10 m from the swim lane) to record the entire session. The recording of the session made it possible to calculate the total times, with the program KINOVEA 0.9.5.

  5. Parcial Time [3 hours after ingestion of the beetroot juice]

    The complete 2x6x100 main test was recorded with a JVC model GY-HM150E video camera placed on the stand of the facility itself at about 10 m from the start/turn wall (approximately 5 m above and 10 m from the swim lane) to record the entire session. The recording of the session made it possible to calculate the split times, with the KINOVEA 0.9.5 program.

  6. Counter Movement Jump [3 hours after ingestion of the beetroot juice]

    Swimmers completed three repetitions of CMJ with hands on waist using an infrared jumping system (Optojump Next, Microgate, Bolzano, Italy)

Secondary Outcome Measures

  1. Stroke rate [from the day of randomization to the last day of the intervention: up to day 7]

    The complete 2x6x100 main test was recorded with a JVC model GY-HM150E video camera placed on the stand of the facility itself at about 10 m from the start/turn wall (approximately 5 m above and 10 m from the swim lane) to record the entire session. The recording of the session made it possible to calculate the stroke rate, with the KINOVEA 0.9.5 program.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 25 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
    • national and international level swimmers
    • healthy swimmers
    • no breakfast
    • 48 hours with restricted diet of: other sports supplements and beetroot-rich foods
Exclusion Criteria:
  1. -be on medication

    • having had breakfast
    • have brushed your teeth

Contacts and Locations

Locations

Site City State Country Postal Code
1 Universidad Francisco de Vitoria Madrid Pozuelo De Alarcón Spain 28223

Sponsors and Collaborators

  • Universidad Francisco de Vitoria
  • Universidad Politécnica de Madrid.
  • Instituto Politécnico de Bragança

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Universidad Francisco de Vitoria
ClinicalTrials.gov Identifier:
NCT05657093
Other Study ID Numbers:
  • 79/2022
First Posted:
Dec 20, 2022
Last Update Posted:
Dec 20, 2022
Last Verified:
Nov 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Universidad Francisco de Vitoria

Study Results

No Results Posted as of Dec 20, 2022