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.
1 other identifier
interventional
12
1 country
1
Brief Summary
Beetroot juice is a rich source of nitrate (NO3-), which serves as a precursor to nitric oxide (NO) via the NO3- to nitrite (NO2-) to NO conversion pathway. This pathway is believed to enhance vasodilation and improve neuromuscular function, such as by increasing sarcoplasmic reticulum calcium release and re-uptake, leading to enhanced force production 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 17, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 24, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2021
CompletedFirst Submitted
Initial submission to the registry
August 27, 2024
CompletedFirst Posted
Study publicly available on registry
November 5, 2024
CompletedNovember 5, 2024
August 1, 2024
7 days
August 27, 2024
November 4, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Tensiomyography changes (seconds): Delay time (Td) ; Contraction time (Tc) ; Sustain time (Ts) ; Relaxation time (Tr)
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.
1-week
Changes in 60-m and 100-m sprint test (seconds)
Time to complete 60-m and 100-m sprint test using photocell timing gates
1-week
Secondary Outcomes (4)
Changes in maximal countermovement and squat jump height (cm)
1-week.
Changes in nitrites and nitrates levels in saliva (μmol/L)
1-week
Changes in side effects questionnarie
1-week
Changes in rate of perception effort
1-week
Study Arms (2)
Beetroot juice supplementation
EXPERIMENTALOne 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.
Placebo supplementation
PLACEBO COMPARATOROne 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.
Interventions
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.
Eligibility Criteria
You may qualify if:
- Between 18 to 40 years old.
- With a regular training practise in track and field disciplines \> 5 years.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Universidad Pontificia Comillaslead
- Universidad Francisco de Vitoriacollaborator
- Universidad de Leóncollaborator
- Anglia Ruskin Universitycollaborator
- Universidad Rey Juan Carloscollaborator
Study Sites (1)
Universidad Pontificia Comillas
Madrid, Spain
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Alvaro López Samanes, PhD
Universidad Pontificia Comillas
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 27, 2024
First Posted
November 5, 2024
Study Start
March 17, 2021
Primary Completion
March 24, 2021
Study Completion
March 31, 2021
Last Updated
November 5, 2024
Record last verified: 2024-08