- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07473193
Beetroot Beverage and Repeated Sprint Power Output During RAST
"Effects of a Beetroot-Based Functional Beverage on Repeated Sprint Performance: A Randomized, Double-Blind, Placebo-Controlled Crossover Trial"
This randomized, double-blind, placebo-controlled crossover trial aims to evaluate the acute effects of a nitrate-rich beetroot-based beverage on repeated sprint performance in trained athletes.
Ten athletes will complete two experimental conditions in randomized order: beetroot beverage (BET) and placebo (PLA), separated by a 7-day washout period. The beetroot beverage consists of 200 mL of a mixture containing beetroot, cocoa, and green tea, providing approximately 6.4 mmol of nitrate.
In each condition, participants will perform a Running Anaerobic Sprint Test (RAST), consisting of six maximal 35-meter sprints with 10 seconds of passive recovery between sprints. The primary outcome is mean power output across the six sprints.
Secondary outcomes include fatigue index, sprint-by-sprint power output, heart rate, rating of perceived exertion (Borg 6-20 scale), maximal oxygen uptake (VO₂max), and sleep quality assessed using the Insomnia Severity Index (ISI).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This randomized, double-blind, placebo-controlled crossover trial is designed to investigate the acute effects of a nitrate-rich beetroot-based beverage on repeated sprint performance in trained athletes.
Ten athletes will participate in two experimental sessions in randomized order: beetroot beverage (BET) and placebo (PLA). Randomization will determine the sequence of beverage administration. Participants and investigators will be blinded to treatment allocation.
After beverage ingestion, participants will perform a standardized warm-up followed by the Running Anaerobic Sprint Test (RAST), consisting of six maximal 35-meter sprints with 10 seconds of passive recovery between sprints. Sprint time will be recorded using electronic timing, and power output will be calculated using body mass and sprint time.
The primary outcome measure is mean power output across all six sprints. Secondary outcomes include:
Fatigue index (percentage decrement across sprints)
Individual sprint power (S1-S6)
Heart rate response
Rating of perceived exertion (Borg 6-20 scale)
VO₂max (assessed at baseline)
Sleep quality measured using the Insomnia Severity Index (ISI)
A linear mixed-effects model will be used to analyze repeated sprint performance, including subject as a random intercept and treatment, sprint, and their interaction as fixed effects. Non-parametric tests will be applied when assumptions of normality are not met. Statistical significance will be set at p ≤ 0.05.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Emmanuel Omar Ponce Dávila, MC
- Phone Number: +526142715782
- Email: a327789@uach.mx
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy trained athletes
Age between 18-35 years
Regular training ≥3 times/week
No cardiovascular or metabolic disease
Exclusion Criteria:Healthy trained athletes
Age between 18-35 years
Regular training ≥3 times/week
No cardiovascular or metabolic disease
-
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 Beverage (BET)
Participants consumed 200 mL of a beetroot-based antioxidant beverage containing beetroot, cocoa, and green tea extract, providing approximately 6.4 mmol of dietary nitrate.
The beverage was ingested 2-3 hours before performing the exercise test.
|
Participants consumed 200 mL of a beetroot-based antioxidant beverage containing beetroot, cocoa, and green tea extract, providing approximately 6.4 mmol of dietary nitrate.
The beverage was administered 2-3 hours before performing a Running Anaerobic Sprint Test (RAST).
The formulation was designed to deliver nitrate and polyphenols with potential ergogenic and antioxidant effects.
A 7-day washout period separated crossover conditions.
|
|
Placebo Comparator: Placebo Beverage (PLA)
Participants consumed 200 mL of a placebo beverage matched for color, taste, and texture but without nitrate or active antioxidant compounds.
The beverage was ingested 2-3 hours before performing the exercise test.
|
Participants consumed 200 mL of a beetroot-based antioxidant beverage containing beetroot, cocoa, and green tea extract, providing approximately 6.4 mmol of dietary nitrate.
The beverage was administered 2-3 hours before performing a Running Anaerobic Sprint Test (RAST).
The formulation was designed to deliver nitrate and polyphenols with potential ergogenic and antioxidant effects.
A 7-day washout period separated crossover conditions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean power output (W) during six maximal 35-m sprints
Time Frame: Baseline and immediately post-intervention.
|
Mean power output will be calculated from six maximal 35-m sprint efforts separated by standardized recovery intervals.
Sprint time will be recorded and converted to power output (W).
The mean value across all six sprints will be used as the outcome measure.
|
Baseline and immediately post-intervention.
|
Collaborators and Investigators
Publications and helpful links
General Publications
- Ponce Dávila, E. O., Neder Suárez, D., Muñoz Daw, M. de J., Carrasco Legleu, C. E., & Benítez Hernández, Z. P. (2024). Diseño y análisis de una bebida deportiva a base de betabel. Revista Mexicana De Ciencias De La Cultura Física, 3(7), 1-10. https://doi.org/10.54167/rmccf.v3i7.1370
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- Cl-062-23
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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