- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06073275
Effects of Beetroot Juice Intake on Performance and Physiological Parameters
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
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Barcelona
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Sant Boi De Llobregat, Barcelona, Spain, 08830
- Campus Docent Sant Joan de Déu. Universitat de Barcelona
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- national and/or international level;
- without cardiovascular, respiratory, metabolic, neurological or orthopedic disorders that may affect the performance of the rowing ergometer test;
- no consumption of drugs or medicines;
- no smoking;
- Informed consent to participate in the study signed by all rowers
Exclusion Criteria:
- Ingestion of nutritional supplements taken in the three months prior to the start of the study;
- no following the guidelines established by the nutrition professional.
Study Plan
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).
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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.
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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
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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.
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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
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minutes:seconds (mm:ss)
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through study completion, an average of 3 weeks
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Rowing performance: Mean Power output
Time Frame: through study completion, an average of 3 weeks
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Watts
|
through study completion, an average of 3 weeks
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Rowing performance: meter per stroke
Time Frame: through study completion, an average of 3 weeks
|
Meters
|
through study completion, an average of 3 weeks
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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
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Cardiorespiratory performance: relative oxygen uptake
Time Frame: through study completion, an average of 3 weeks
|
V̇O2max (mL/kg/min)
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through study completion, an average of 3 weeks
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Cardiorespiratory performance: ventilatory efficiency
Time Frame: through study completion, an average of 3 weeks
|
slope of Ventilation/Carbon dioxide production
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through study completion, an average of 3 weeks
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Metabolic performance: lactate
Time Frame: through study completion, an average of 3 weeks
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mmol/L
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through study completion, an average of 3 weeks
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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
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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
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minute ventilation in L/min
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through study completion, an average of 3 weeks
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Scale of Perceived exertion ratio (RPE)
Time Frame: through study completion, an average of 3 weeks
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Scale from 0 to 10. 0 = rest; 10 = maximum effort
|
through study completion, an average of 3 weeks
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Rowing performance: strokes
Time Frame: through study completion, an average of 3 weeks
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Mean strokes per minute
|
through study completion, an average of 3 weeks
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Collaborators and Investigators
Investigators
- Principal Investigator: Manuel V Garnacho-Castaño, PhD, Campus docent Sant Joan de Déu-Universitat de Barcelona
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CDSJD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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