Beetroot Juice and Neuromuscular Performance in Female Basketball Players
BASKET_BEET
Physical Performance Following Multiday Beetroot Juice Supplementation in Female Basketball Players: A Randomized, Double-Blind, Placebo-Controlled, Crossover Study
2 other identifiers
interventional
16
1 country
1
Brief Summary
A randomized, double-blind, placebo-controlled study investigates the effects of 5 days of nitrate-rich beetroot juice supplementation (70 mL·day-¹; 6.4 mmol NO₃-·day-¹) on physical performance in female basketball players. Performance will be evaluated using jump, 30-m sprint, agility, and isometric mid-thigh pull (IMTP) tests, while RPE and potential side effects will be assessed through questionnaires. The study aims to address the limited evidence regarding the ergogenic effects of beetroot juice supplementation in female team-sport 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 Sep 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 16, 2026
CompletedFirst Posted
Study publicly available on registry
September 22, 2026
CompletedStudy Start
First participant enrolled
September 22, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 7, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 15, 2026
September 22, 2026
September 1, 2026
15 days
September 16, 2026
September 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Changes in maximal isometric handgrip strength (N)
Isometric Mid-Thigh Pull (IMTP): Lower-body maximal isometric strength will be assessed using the isometric mid-thigh pull (IMTP) performed on VALD ForceDecks force platforms (VALD Performance, Brisbane, Australia). Participants will adopt a standardized mid-thigh pull position with the knees and hips slightly flexed and will be instructed to pull against an immovable bar as hard and as fast as possible. Ground reaction force will be recorded by the force platforms throughout each maximal effort. Peak force will be expressed both as absolute force (N) and relative to body mass (N·kg-¹). Participants will perform maximal trials separated by an appropriate recovery period, and the best trial will be retained for analysis.
1-week
Changes in maximal jump height (cm)
Maximal Jump Height: Lower-body explosive performance will be assessed using the squat jump (SJ), countermovement jump (CMJ), and countermovement jump with arm swing (CMJ-AS). Jump performance will be measured using an OptoJump Next system (Microgate, Bolzano, Italy). Participants will perform maximal-effort trials for each jump condition following standardized instructions. Maximal jump height (cm) will be recorded for each jump type, and the best performance will be retained for analysis. Changes in maximal jump height following 5 days of supplementation will be compared between the nitrate-rich beetroot juice and placebo conditions.
1-week
Changes in sprint time (s)
Sprint performance will be assessed by measuring the time required to complete 10-m, 20-m, and 30-m sprints using Microgate photocell timing gates (Microgate, Bolzano, Italy). Participants will be instructed to sprint as fast as possible over the 30-m distance, with split times recorded at 10 m, 20 m, and 30 m. Sprint time will be recorded in seconds (s). Participants will perform maximal trials separated by an appropriate recovery period, and the best performance will be retained for analysis.
1-week
Changes in agility test (s)
Modified T-Test Performance: Change-of-direction performance will be assessed using the modified T-test, with completion time measured using Microgate photocell timing gates (Microgate, Bolzano, Italy). Participants will be instructed to complete the standardized course as quickly as possible, incorporating forward sprinting, lateral shuffling, and backward running. Completion time will be recorded in seconds (s). Participants will perform maximal trials separated by an appropriate recovery period, and the best performance will be retained for analysis.
1-week
Secondary Outcomes (3)
Saliva NO3- and NO2- Measurements
1-week
Rating of percevied exertion (RPE) (measured using scale 6-20 points)
1-week
Side Effects Associated With Beetroot Juice Supplementation
1-week
Study Arms (2)
Experimental: Beetroot juice supplementation
EXPERIMENTALParticipants consumed one serving of 70 mL of nitrate-rich BJ (6.4 mmol of NO₃-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) was administered daily for 5 consecutive days. On the final supplementation day, the placebo was consumed 3 h before the testing session
Placebo supplementation
PLACEBO COMPARATORParticipants consumed one 70-mL serving of nitrate-depleted beetroot juice placebo (0.04 mmol of NO₃-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) daily for 5 consecutive days. On the final supplementation day, the placebo was consumed 3 h before the testing session.
Interventions
Participants consumed one 70-mL serving of nitrate-depleted beetroot juice placebo (0.04 mmol of NO₃-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) daily for 5 consecutive days.
Participants consumed one 70-mL serving of nitrate-rich BJ (6.4 mmol of NO₃-; Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) daily for 5 consecutive days. On the final supplementation day, BJ was consumed 3 h before the testing session.
Eligibility Criteria
You may qualify if:
- Female basketball players aged 18-35 years.
- Currently participating in natitional competitive basketball.
- Able to complete all supplementation and testing procedures.
You may not qualify if:
- Presence of any chronic disease or medical condition that could affect physical performance or interfere with the study procedures.
- Presence of any injury during the month prior to the study that could limit participation in the physical performance tests.
- Known intolerance or allergy to beetroot or other nitrate-rich vegetables (e.g., beetroot, lettuce).
- Use of medications or dietary supplements that could potentially influence nitrate metabolism or physical performance during the study period.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Universidad Pontificia Comillaslead
- Universidad Francisco de Vitoriacollaborator
- Central Queensland Universitycollaborator
- Universidad Complutense de Madridcollaborator
- Universidad de Cadizcollaborator
- University of Tehrancollaborator
Study Sites (1)
Universidad Pontificia Comillas
Madrid, Madrid, 20815, Spain
Related Publications (1)
Lopez-Samanes A, Perez-Lopez A, Morencos E, Munoz A, Kuhn A, Sanchez-Migallon V, Moreno-Perez V, Gonzalez-Frutos P, Bach-Faig A, Roberts J, Dominguez R. Beetroot juice ingestion does not improve neuromuscular performance and match-play demands in elite female hockey players: a randomized, double-blind, placebo-controlled study. Eur J Nutr. 2023 Apr;62(3):1123-1130. doi: 10.1007/s00394-022-03052-1. Epub 2022 Nov 19.
PMID: 36401662BACKGROUND
Study Officials
- STUDY CHAIR
Alvaro Lopez 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
- Masking Details
- In addition to the participants, the investigators responsible for performance testing and data analysis will remain blinded to group allocation until completion of data collection and statistical analyses.
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 16, 2026
First Posted
September 22, 2026
Study Start
September 22, 2026
Primary Completion (Estimated)
October 7, 2026
Study Completion (Estimated)
October 15, 2026
Last Updated
September 22, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be publicly shared to protect participant confidentiality and privacy. The study involves a relatively small and specific sample of competitive female basketball players, which could increase the potential risk of participant identification. Aggregated and anonymized study results will be reported in scientific publications and presentations.