Effects of Beetroot Juice Intake on Performance and Physiological Parameters
NCT ID: NCT06073275
Last Updated: 2023-10-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2018-11-01
2019-02-26
Brief Summary
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In both strictly identical sessions, the participants randomly ingested beetroot juice (BRJ) or placebo (PL) 3 hours before the start of the tests.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
OTHER
TRIPLE
Study Groups
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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
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 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
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.
Interventions
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Beetroot juice ingestion
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 ingestion
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.
Eligibility Criteria
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Inclusion Criteria
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
2. no following the guidelines established by the nutrition professional.
30 Years
MALE
Yes
Sponsors
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Campus docent Sant Joan de Déu-Universitat de Barcelona
OTHER
Responsible Party
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Manuel Vicente Garnacho Castano
Principal investigator
Principal Investigators
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Manuel V Garnacho-Castaño, PhD
Role: PRINCIPAL_INVESTIGATOR
Campus docent Sant Joan de Déu-Universitat de Barcelona
Locations
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Campus Docent Sant Joan de Déu. Universitat de Barcelona
Sant Boi de Llobregat, Barcelona, Spain
Countries
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Other Identifiers
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CDSJD
Identifier Type: -
Identifier Source: org_study_id
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