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Completed

NCT Number: NCT06349018

Effects of Isotonic Beetroot Supplementation on Sprint Interval Exercise Performance

This study aims to examine the effects of dietary nitrate supplementation via beetroot juice on sprint interval cycling exercise performance. Twenty-four participants (male or female) will undertake a randomized, crossover trial where they consume either (i) an isotonic beetroot juice drink containing nitrate (12.9 mmol) for 5 days or (ii) an isotonic sports drink (no nitrate) for 5 days. On Day 5 of each trial, participants will come to the laboratory and 2 hours after consuming their allocated drink will complete a 6 bouts of sprint interval exercise. Power output during cycling will be measured as the primary outcome measure. Salivary and plasma measures of nitrate and nitrite will be taken over the course of the morning on Day 5. After a 5-day washout period participants will crossover and begin their second trial.

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Key information

Age range

21 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Human Bioenergetics Laboratory, National Institute of Education, Nanyang Technological University

Singapore, 637616

About this study

This study aims to examine the effects of dietary nitrate supplementation via beetroot juice on sprint interval cycling exercise performance. Twenty-four participants (male or female) will undertake a randomized, crossover trial where they consume either (i) an isotonic beetroot juice drink containing nitrate (12.9 mmol) for 5 days or (ii) an isotonic sports drink (no nitrate) for 5 days. Drinks will be equivalent in isotonicity and colored the same so that participants and investigators will be blinded to each trial. Randomization and drink allocation will be completed by a third person not associated with the study team. On Day 5 of each trial, participants will come to the laboratory and 2 hours after consuming their allocated drink will complete a 6 bouts of sprint interval exercise (10 second all-out maximal sprints interspersed with 50 seconds rest). Power output (peak and mean) during cycling sprints will be measured as the primary outcome measure. Salivary measures of nitrate/nitrite will be taken at three time points over the course of the morning on Day 5 - (i) pre-drink consumption; (ii) 2 hours post-drink consumption; and (iii) post-exercise. Plasma measures of nitrate and nitrite will be taken at two time points over the course of the morning on Day 5 - (i) pre-drink consumption; and (ii) 2 hours post-drink consumption. Near infra-red spectroscopy (NIRS) will be used to measure muscle (vastus lateralis) oxygenation during cycling bouts. A Stroop test to measure inhibition (executive function) will be taken pre- and post-exercise. Sensory perception of the drink will be measured immediately post-consumption on Day 5. After a 5-day washout period participants will crossover and begin their second trial.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 21 - 40 years
  • Healthy and injury-free (e.g., no cardiovascular disease, diabetes mellitus, orthopaedic impairment that interferes with moderate-to-vigorous exercise)
  • Blood pressure < 130/90 mmHg
  • Be physically active: Engaging in a minimum of 150 minutes of moderate-intensity exercise or 75 minutes of vigorous-intensity physical activity each week.
  • Recreational cyclist (Minimum 1 hour cycling per week).
  • Body mass index: 18.5-25 kg/m2
  • Non-smoker
  • Asian

Exclusion criteria

  • Any allergies to beetroot or isotonic drink.
  • Asthma
  • Any diagnosed form of cardiometabolic disease (heart disease, stroke, peripheral vascular disease, diabetes, metabolic syndrome, high blood pressure).
  • Any symptoms contraindicating exercise testing (e.g. chest pains).
  • Any balance or dizziness problems.
  • Any chronic medical conditions (whether medicated or not).
  • Any bone joint problems.
  • Any Physician diagnosed contraindications to exercise.
  • Any other health problems that may be a cause for concern or contraindication to exercise.
  • Any recent Covid vaccination (within last 2 weeks).

Treatment and study plan

Dietary Supplement: High nitrate isotonic drink

Other

High nitrate (12.9 mmol) drink with carbohydrate and minerals

Dietary Supplement: No nitrate isotonic drink

Other

Carbohydrate and mineral isotonic drink

Primary outcomes

  1. Power output during maximal sprint cycling

    Time frame: 2 hours after drink ingestion

    Peak and mean power output

Secondary outcomes

  1. Salivary nitrate

    Time frame: Pre-drink, 2 hours post-drink and immediately post-exercise (2.5 hours post-drink)

    Salivary nitrate/nitrite concentration

  2. Plasma nitrate and nitrite

    Time frame: Pre-drink and 2 hours post-drink

    Plasma nitrate and nitrite

  3. Muscle oxygenation

    Time frame: During exercise (2-2.5 hours post drink)

    Near infra-red spectroscopy

  4. Sensory evaluation (Acceptance and Preference Test Evaluation by Meilgaard et al 2007)

    Time frame: Immediately post-drink (1 minute post-drink)

    Drink taste and perception (7-point scale - 1 extremely dislike to 7 extremely like)

  5. Stroop test

    Time frame: Immediately pre- (2 hours post-drink) and immediately post-exercise (2.5 hours post drink)

    Reaction time and correct answers

Sponsors and collaborators

Lead sponsor

Nanyang Technological University

Other

Registry information

Official study title

The Effects of Isotonic Beetroot Supplementation on Sprint Interval Exercise Performance.

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Apr 5, 2024
Registry last updated
Apr 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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