- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06675682
Beetroot Juice Effects on Contractile or Neuromuscular Properties in Male Trained Sprinters (BEET_SPRINT)
Acute Ingestion of Beetroot Juice Does Effects on Contractile or Neuromuscular Properties in Male Trained Sprinters: a Randomized, Double-blind, Placebo-controlled Study.
Study Overview
Status
Intervention / Treatment
Detailed Description
Sports nutrition is a rapidly expanding scientific field that has experienced a significant increase in interest from the academic community over the past decade. Despite the extensive marketing of numerous nutritional products that claim to optimize athlete health, function, and performance, only a limited number of sports foods or dietary supplements have been supported by robust evidence for enhancing performance. Among these, caffeine, creatine, beetroot juice, β-alanine, and bicarbonate are notable for their validated efficacy, though the effectiveness of these supplements can vary based on the specific event, context of use, and the individual athlete's goals and responsiveness.
Beetroot juice, in particular, is a rich source of nitrate (NO3-), which serves as a precursor to nitric oxide (NO) through the NO3- to nitrite (NO2-) to NO conversion pathway. This pathway is believed to promote vasodilation and improve neuromuscular function, such as by increasing sarcoplasmic reticulum calcium release and re-uptake, leading to enhanced force output in type II muscle fibers and improved muscle contractile recruitment. Therefore, the aim of this study was to investigate the effects of beetroot juice supplementation on muscle contractile properties, as assessed by tensiomyography, and neuromuscular performance in sprint-trained athletes. The goal was to gain a deeper understanding of the physiological effects induced by beetroot juice intake in short-distance track and field disciplines.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Madrid, Spain
- Universidad Pontificia Comillas
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Between 18 to 40 years old.
- With a regular training practise in track and field disciplines > 5 years.
Exclusion Criteria:
- Intolerance to beetroot juice or NO3- derivatives
- Presence of any chronic pathology or injury within three months prior to the study-
- Use of medications or supplements (e.g., caffeine) during the study.
- Failure to attend all experimental sessions.
- Failure to adhere to the dietary guidelines established in the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Beetroot juice supplementation
One serving 70 mL of beetroot juice (6.4 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) 2.5 h before initiating the testing session.
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Player randomization was performed using an online tool (https://www.randomizer.org/).
An independent researcher assigned alphanumeric codes to each sequence to ensure blinding of both sprint athletes and researchers during the trials.
Each player participated in two identical experimental trials separated by one week to allow physical recovery between testing occasions and washout from the beetroot juice treatment.
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Placebo Comparator: Placebo supplementation
One serving 70 mL of beetroot juice placebo (0.04 mmol of NO3-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) 2.5 h before initiating the testing session.
|
Player randomization was performed using an online tool (https://www.randomizer.org/).
An independent researcher assigned alphanumeric codes to each sequence to ensure blinding of both sprint athletes and researchers during the trials.
Each player participated in two identical experimental trials separated by one week to allow physical recovery between testing occasions and washout from the beetroot juice treatment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Tensiomyography changes (seconds): Delay time (Td) ; Contraction time (Tc) ; Sustain time (Ts) ; Relaxation time (Tr)
Time Frame: 1-week
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The measurement of the rectus femoris, biceps femoris, gastrocnemius lateralis, and gastrocnemius medialis muscles was conducted using tensiomyography.
We analyzed different parameters such as selay time (Td) as a time between the electrical impulse and 10% of the contraction; Contraction time (Tc) as a time between 10% and 90% of the contraction; Sustain time (Ts) as a time between 50% of the contraction and 50% of the relaxation; Relaxation time (Tr) as a time between 90% and 50% of the relaxation.
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1-week
|
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Changes in 60-m and 100-m sprint test (seconds)
Time Frame: 1-week
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Time to complete 60-m and 100-m sprint test using photocell timing gates
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1-week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in maximal countermovement and squat jump height (cm)
Time Frame: 1-week.
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Maximal jump height using a contact platform
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1-week.
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Changes in nitrites and nitrates levels in saliva (μmol/L)
Time Frame: 1-week
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Using specific kit ELISA analysis
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1-week
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Changes in side effects questionnarie
Time Frame: 1-week
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Questionnarie based on side-effects related to beetroot juice ingestion (A scale consisting of nine items, each answered with "yes" or "no")
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1-week
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Changes in rate of perception effort
Time Frame: 1-week
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Using rate of perceived exertion scale (1-10 points)
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1-week
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Alvaro López Samanes, PhD, Universidad Pontificia Comillas
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 (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- UPC_Comillas
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
product manufactured in and exported from the U.S.
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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