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Enrolling by invitationNCT07833579BASKET_BEETUpdated Nov 3, 2026

Beetroot Juice and Neuromuscular Performance in Female Basketball Players

An interventional study of Placebo and Beetroot juice supplementation in Nitrate and Placebo - Control, sponsored by Universidad Pontificia Comillas. Enrolling by invitation at 1 site in Spain. Open to female participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by Universidad Pontificia Comillas · Not applicable, Interventional, and Treatment

Updated Nov 3, 2026Primary completion movedStudy completion moved+1 moreGo to Updates ↓

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Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
Female
01

Study 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.

Read the detailed description

Although beetroot juice supplementation, primarily due to its high inorganic nitrate (NO₃-) content, has been associated with improvements in endurance and high-intensity intermittent exercise performance, its potential ergogenic effects in team sports remain unclear, particularly in female athletes. This knowledge gap is especially relevant in basketball, a sport characterized by repeated bouts of sprinting, jumping, accelerating, decelerating, and changing direction. Therefore, this randomized, double-blind, placebo-controlled study aimed to investigate the effects of 5 consecutive days of nitrate-rich beetroot juice supplementation (70 mL·day-¹, providing 6.4 mmol NO₃-·day-¹) on physical performance in female basketball players. Following the supplementation period, performance was assessed through jumping performance, 30-m sprint, agility, and isometric mid-thigh pull (IMTP) tests. Additionally, rating of perceived exertion (RPE) and potential side effects associated with beetroot juice supplementation were assessed using questionnaires.

02

Conditions studied

  • Nitrate
  • Placebo - Control

Keywords

  • nitrate
  • beetroot
  • team sports
  • female athletes
03

In context

Lead sponsor

Universidad Pontificia Comillas is the lead sponsor of 19 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Female basketball players aged 18-35 years.
  • Currently participating in natitional competitive basketball.
  • Able to complete all supplementation and testing procedures.

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
16 participants (estimated)

Study arms

  • Experimental
    Experimental: Beetroot juice supplementation

    Participants 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

    Dietary Supplement: Beetroot juice supplementation

  • Placebo comparator
    Placebo supplementation

    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. On the final supplementation day, the placebo was consumed 3 h before the testing session.

    Other: Placebo

Interventions

  • OtherPlacebo

    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.

  • Dietary supplementBeetroot juice supplementation

    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.

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: 1-week

  2. 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.

    Time frame: 1-week

  3. 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.

    Time frame: 1-week

  4. 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.

    Time frame: 1-week

Secondary outcomes

  1. Saliva NO3- and NO2- Measurements

    Saliva samples were collected 150 min after BJ or the placebo ingestion and were stored at -20°C for four months until subsequent analysis. To confirm the effectiveness of BJ supplementation on nitrate (NO3-) and nitrite (NO2-) levels, saliva concentrations were measured using a nitric oxide assay kit (EMSNO K195325, Thermo Fisher Scientific, Roskilde, Denmark) according to the manufacturer's instructions and as reported in previous literature (Richard et al., 2018). All samples and standards were measured in duplicate and averaged.

    Time frame: 1-week

  2. Rating of percevied exertion (RPE) (measured using scale 6-20 points)

    Immediately after each physical performance battery, participants were asked for providing her RPE using a Borg scale from 6 to 20 points

    Time frame: 1-week

  3. Side Effects Associated With Beetroot Juice Supplementation

    The morning after the supplementation and testing session, participants will complete a questionnaire assessing potential side effects associated with beetroot juice or placebo ingestion. The questionnaire includes gastrointestinal upset, red urine, gastric reflux, mild nausea, muscle pain, headache, increased urine excretion, increased fatigue, and nervousness. Each side effect will be assessed using a dichotomous Yes/No response scale (No = 0; Yes = 1). The incidence of each side effect will be reported as the number and percentage of participants reporting the symptom.

    Time frame: 1-week

07

Study locations

1 site
08

References and documents

Publications

  • 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. PubMed 36401662 ↗

Individual participant data

Plan to share: No — 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.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it moved

Ran from Sep 2026 to primary completion in Oct 2026, 1 month.

Completion moved once since we started tracking on Sep 25, 2026: Oct 2026 → Nov 2026, on Nov 3, 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Sep 16, 2026
First posted
Sep 22, 2026
StartActual
Sep 22, 2026
Primary completionActual
Oct 28, 2026
CompletionEst.
Nov 10, 2026was Oct 2026
Last update
Nov 3, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Primary completion
Oct 7, 2026→Oct 28, 2026 (actual)
Nov 3, 2026
Study completion
Oct 15, 2026→Nov 10, 2026
Nov 3, 2026
Sponsor
Collaborators added: University of Cadiz; collaborators removed: Universidad de Cadiz
Nov 3, 2026
Show all 1 update
  1. Nov 3, 2026
    Primary completion Oct 7, 2026→Oct 28, 2026 (now actual)
    Study completion Oct 15, 2026→Nov 10, 2026
    Sponsor Collaborators added: University of Cadiz; collaborators removed: Universidad de Cadiz

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07833579
Lead sponsor
Universidad Pontificia Comillas
Collaborators
Universidad Francisco de Vitoria, Central Queensland University, Universidad Complutense de Madrid, University of Tehran, University of Cadiz
Responsible party
Sponsor
First posted
Sep 22, 2026
Start date
Sep 22, 2026
Primary completion
Oct 28, 2026
Completion
Nov 10, 2026 (estimated)
Last update
Nov 3, 2026

Study contacts

Alvaro Lopez Samanes, PhD
study chair · Universidad Pontificia Comillas

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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