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Exercise PhysiologyNCT07840014

Effects of Acute Beetroot Juice on Aerobic Performance and Muscle Oxygenation in Amateur Female Soccer Players

A study testing Nitrate-rich beetroot juice in people with Exercise Physiology and Sports Nutrition, run by Sakarya Applied Sciences University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Effects of Acute Beetroot Juice on Aerobic Performance and Muscle Oxygenation in Amateur Female Soccer Players Read more about this study

Who is it for?
Ages 18 years and older, women onlyHealthy volunteers can take part
What is being tested?
Nitrate-rich beetroot juice
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
13 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Aug 2025to 2 Sep 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Female
  • Aged 18 years or older
  • Licensed soccer player for at least 3 years

Who cannot join

  • Use of pharmacological treatment or supplements/ergogenic aids that could affect exercise performance, including stimulants such as caffeine
  • Presence of musculoskeletal, ligament, bone, neurological, or joint pathology incompatible with the exercise protocol
  • Current cardiovascular problems
  • Participation in additional sports or physical activities during the study period that could affect the study outcomes

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Sakarya University of Applied Sciences Esentepe Campus Sports Sciences Faculty

    Sakarya

Other trials in Turkey (Türkiye)

About this study

Official title: Effects of Acute Beetroot Juice Supplementation on Aerobic Performance, Muscle Oxygenation, and Physiological Responses in Amateur Female Soccer Players

Effects of Acute Beetroot Juice on Aerobic Performance and Muscle Oxygenation in Amateur Female Soccer Players

Read the detailed description

This randomized, double-blind, placebo-controlled crossover study evaluated the acute effects of nitrate-rich beetroot juice supplementation on aerobic performance, muscle oxygenation, and selected physiological responses in amateur female soccer players.

Thirteen participants completed two experimental conditions in randomized order, separated by a 7-day washout period. In one condition, participants consumed 70 mL of nitrate-rich beetroot juice containing 6.4 mmol of nitrate, while in the other condition they consumed an equal volume of low-nitrate blackcurrant placebo containing <0.1 mmol of nitrate. Each beverage was consumed 2.5 hours before exercise testing.

Aerobic performance was assessed using a treadmill-adapted 12-minute Cooper test. Total distance covered and estimated maximal oxygen uptake (VO₂max) were evaluated as performance outcomes. Muscle oxygen saturation was monitored using near-infrared spectroscopy. Heart rate, blood pressure, blood glucose, and rating of perceived exertion were also assessed at predefined time points. Participants and investigators conducting the experimental procedures were blinded to the supplementation condition, and the supplementation sequence was generated by an independent researcher who was not involved in the experimental procedures or statistical analyses.

Being tested
Nitrate-rich beetroot juice, Low-nitrate blackcurrant placebo beverage
Keywords
Beetroot juice, Dietary nitrate, Aerobic performance, Muscle oxygenation, Female soccer players

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nitrate-rich beetroot juiceDietary supplement

    Participants consumed a single 70 mL dose of nitrate-rich beetroot juice (Beet It Pro Elite Shot, James White Drinks Ltd., Ipswich, UK) containing 6.4 mmol (approximately 400 mg) of nitrate. The supplement was ingested 2.5 hours before the 12-minute exercise test.

  • Low-nitrate blackcurrant placebo beverageOther

    Participants consumed a single 70 mL dose of low-calorie blackcurrant beverage (Pfanner, Austria) containing negligible nitrate (<0.1 mmol). The placebo was ingested 2.5 hours before the 12-minute exercise test.

Study groups in NCT07840014
Study groupRoleWhat they receive
Beetroot Juice, Then PlaceboExperimentalParticipants first received 70 mL of nitrate-rich beetroot juice containing 6.4 mmol nitrate. After a 7-day washout period, they received 70 mL of low-nitrate blackcurrant placebo containing <0.1 mmol nitrate. Each beverage was consumed 2.5 hours before the 12-minute exercise test.
Receives: Dietary Supplement: Nitrate-rich beetroot juice; Other: Low-nitrate blackcurrant placebo beverage
Placebo,Then Beetroot JuiceExperimentalParticipants first received 70 mL of low-nitrate blackcurrant placebo containing <0.1 mmol nitrate. After a 7-day washout period, they received 70 mL of nitrate-rich beetroot juice containing 6.4 mmol nitrate. Each beverage was consumed 2.5 hours before the 12-minute exercise test.
Receives: Dietary Supplement: Nitrate-rich beetroot juice; Other: Low-nitrate blackcurrant placebo beverage

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Distance Covered During the 12-Minute Cooper Test

    Total distance covered, expressed in meters, during a self-paced treadmill-adapted 12-minute Cooper test. Participants were instructed to cover the greatest possible distance within 12 minutes and were allowed to adjust treadmill speed throughout the test.

    Measured: During the 12-minute exercise test performed 2.5 hours after supplementation in each crossover condition

Secondary outcomes (6)
  1. Estimated Maximal Oxygen Uptake (VO₂max)

    Estimated maximal oxygen uptake (VO₂max), expressed as mL·kg-¹·min-¹, was calculated from the total distance covered during the treadmill-adapted 12-minute Cooper test using the classical Cooper equation.

    Measured: At completion of the 12-minute exercise test performed 2.5 hours after supplementation in each crossover condition.

  2. Muscle Oxygen Saturation (SmO₂)

    Muscle oxygen saturation (SmO₂), expressed as a percentage, was assessed in the vastus lateralis using near-infrared spectroscopy (Moxy Monitor, Fortiori Design LLC, Spicer, MN, USA).

    Measured: Baseline (2 minutes before warm-up), during the 12-minute exercise test, and early post-exercise (approximately 2-3 minutes after exercise) in each crossover condition.

  3. Heart Rate

    Heart rate, expressed as beats per minute, was recorded using a Polar V800 heart rate monitor. Values were summarized as the 1-minute pre-exercise mean, mean heart rate during the 12-minute exercise test, and recovery heart rate.

    Measured: Pre-exercise, continuously during the 12-minute exercise test, approximately 2-3 minutes post-exercise, and approximately 29-30 minutes post-exercise in each crossover condition.

  4. Blood Pressure

    Blood pressure, expressed in mmHg, was measured using an automated blood pressure monitor (Omron M2, Omron Healthcare Co., Kyoto, Japan). Three consecutive readings were obtained at each time point and averaged.

    Measured: Before supplementation, pre-exercise, 3 minutes post-exercise, and 30 minutes post-exercise in each crossover condition.

  5. Blood Glucose

    Capillary blood glucose, expressed in mg/dL, was measured from a finger-prick blood sample using a portable glucose analyzer (Plusmed Accuro, Taiwan).

    Measured: Immediately before supplementation, pre-exercise (2 minutes before warm-up), and immediately post-exercise in each crossover condition.

  6. Rating of Perceived Exertion (RPE)

    Rating of perceived exertion was assessed using the Borg 6-20 scale, where higher scores indicate greater perceived exertion.

    Measured: Baseline and immediately post-exercise in each crossover condition.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Sep 2026
  2. Study start1 Aug 2025
  3. Primary completion2 Sep 2025
  4. Study completion2 Sep 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Crossover
Model description
Participants completed both intervention conditions in randomized order. Each participant received beetroot juice in one period and placebo in the other, with a 7-day washout period between conditions.
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
13 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07840014
Sponsor's protocol ID
SUBU-BJ-2025-01
Status last verified
Sep 2026
First submitted
15 Sep 2026
Last updated
24 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The data supporting the findings of this study are available from the corresponding author upon reasonable request, subject to ethical and privacy considerations.

Questions about this trial

What is this clinical trial studying?

A study testing Nitrate-rich beetroot juice in people with Exercise Physiology and Sports Nutrition, run by Sakarya Applied Sciences University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Distance Covered During the 12-Minute Cooper Test (time frame: During the 12-minute exercise test performed 2.5 hours after supplementation in each crossover condition). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Sep 2026; AzTrials last refreshed its copy on 7 Nov 2026.

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