Effects of Beetroot Juice Intake on Performance and Physiological Parameters

October 7, 2023 updated by: Manuel Vicente Garnacho Castano, Campus docent Sant Joan de Déu-Universitat de Barcelona

Effects of Acute Beetroot Juice Intake on Performance, Maximal Oxygen Uptake, and Ventilatory Efficiency in Well-trained Master Rowers: A Randomized, Double-blinded Crossover Study

This study was a randomized, double-blind, crossover design for 3 weeks. In the first week, a researcher explained all the experimental procedures to the participants. In the following two weeks, the participants attended the Exercise Physiology laboratory to be assessed in 2 rowing ergometer sessions, separated from each other by a washout period of 7 days, under the same environmental conditions.

In both strictly identical sessions, the participants randomly ingested beetroot juice (BRJ) or placebo (PL) 3 hours before the start of the tests.

Study Overview

Detailed Description

Three hours after BRJ or PL intake, the participants began the 2,000-meter rowing ergometer test. Before starting (pretest) and at the end of the tests (posttest), blood oxygen saturation, rating of perceived exertion (RPE), and blood lactate measurements were taken. During the rowing ergometer tests, performance parameters and cardiorespiratory variables were recorded.

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

    • Barcelona
      • Sant Boi De Llobregat, Barcelona, Spain, 08830
        • Campus Docent Sant Joan de Déu. Universitat de Barcelona

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. national and/or international level;
  2. without cardiovascular, respiratory, metabolic, neurological or orthopedic disorders that may affect the performance of the rowing ergometer test;
  3. no consumption of drugs or medicines;
  4. no smoking;
  5. Informed consent to participate in the study signed by all rowers

Exclusion Criteria:

  1. Ingestion of nutritional supplements taken in the three months prior to the start of the study;
  2. no following the guidelines established by the nutrition professional.

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: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Beetroot juice intake
Beetroot juice was administered 3 h before the start of the rowing ergometer test since the peak of nitrite in the blood occurs 2-3 h after nitrate ingestion. Beetroot juice was provided in a 140 mL maroon plastic bottle with no label. Participants were provided with a randomized bottle containing 140 mL (~12.8 mmol, ~808 mg of nitrate) of BRJ Beet-It-Pro Elite Shot concentrate (Beet IT; James White Drinks Ltd., Ipswich, UK).
Beetroot juice ingestion was randomly administered 3 h before the start of the test to the participants in two assessment sessions with a one-week washout between both sessions.
Placebo Comparator: Placebo intake
Placebo was administered 3 h before the start of the rowing ergometer test. Placebo was provided in a 140 mL maroon plastic bottle with no label. Participants were provided with a randomized bottle containing 140 mL. The placebo drink was made by dissolving in 1 liter of water 2g of powdered SUPER BEETROOT (~ 0.01 mmol, 0.620 mg of nitrate, diet, food, Poland), 100% natural beetroot juice and organic label, and adding lemon juice to imitate the flavor and texture of the beetroot juice drink
Placebo ingestion was randomly administered 3 h before the start of the test to the participants in two assessment sessions with a one-week washout between both sessions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rowing performance: Time trial
Time Frame: through study completion, an average of 3 weeks
minutes:seconds (mm:ss)
through study completion, an average of 3 weeks
Rowing performance: Mean Power output
Time Frame: through study completion, an average of 3 weeks
Watts
through study completion, an average of 3 weeks
Rowing performance: meter per stroke
Time Frame: through study completion, an average of 3 weeks
Meters
through study completion, an average of 3 weeks
Cardiorespiratory performance: absolute oxygen uptake
Time Frame: through study completion, an average of 3 weeks
V̇O2max (L/min)
through study completion, an average of 3 weeks
Cardiorespiratory performance: relative oxygen uptake
Time Frame: through study completion, an average of 3 weeks
V̇O2max (mL/kg/min)
through study completion, an average of 3 weeks
Cardiorespiratory performance: ventilatory efficiency
Time Frame: through study completion, an average of 3 weeks
slope of Ventilation/Carbon dioxide production
through study completion, an average of 3 weeks
Metabolic performance: lactate
Time Frame: through study completion, an average of 3 weeks
mmol/L
through study completion, an average of 3 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cardiorespiratory performance: Maximum heart rate
Time Frame: through study completion, an average of 3 weeks
beats/min
through study completion, an average of 3 weeks
Cardiorespiratory performance: Mean heart rate
Time Frame: through study completion, an average of 3 weeks
beats/min
through study completion, an average of 3 weeks
Saturation
Time Frame: through study completion, an average of 3 weeks
percentage
through study completion, an average of 3 weeks
Cardiorespiratory performance: minute ventilation
Time Frame: through study completion, an average of 3 weeks
minute ventilation in L/min
through study completion, an average of 3 weeks
Scale of Perceived exertion ratio (RPE)
Time Frame: through study completion, an average of 3 weeks
Scale from 0 to 10. 0 = rest; 10 = maximum effort
through study completion, an average of 3 weeks
Rowing performance: strokes
Time Frame: through study completion, an average of 3 weeks
Mean strokes per minute
through study completion, an average of 3 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Manuel V Garnacho-Castaño, PhD, Campus docent Sant Joan de Déu-Universitat de Barcelona

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)

November 1, 2018

Primary Completion (Actual)

January 31, 2019

Study Completion (Actual)

February 26, 2019

Study Registration Dates

First Submitted

September 25, 2023

First Submitted That Met QC Criteria

October 2, 2023

First Posted (Actual)

October 10, 2023

Study Record Updates

Last Update Posted (Actual)

October 10, 2023

Last Update Submitted That Met QC Criteria

October 7, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

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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