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Completed

NCT Number: NCT06531070

Nitrate Formulations and Exercise Performance

this study compares the acute effects of Nitrate and Nitrate plus citrulline supplementation on physical performance in recreationally trained males and females. This is a cross-over within-participant comparison design concluding three arms (i) 600 mg of Nitrate (N), ii) 600 mg Nitrate and Citrulline (NC) and (iii) Placebo (PL).

Conditions N, NC and PL will be tested one week apart, considering a minimum washout period of 72 hours.

Dependent variables:

* Number of completed repetitions to failure in squat using 75% of 1RM. * Ventilatory thresholds (VT1) and (VT2) and Vo2 max from a progressive to exhaustion running test (PGT) * Lactate post (within 1 min of having completed the PGT) * Rating of perceived exertion (RPE) by the Borg 6-to-20-point scale recorded every 2 min and at the end of the PGT. * Heart rate associated with VT1, VT2, and Vo2max - Heart rate maximum. * Maximal aerobic speed (MAS): calculated from the average speed of the last 2 minutes of the PGT. * time limit test at MAS (conducted after 15 min of having completed the PGT)

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Sparrows Farm

Eltham, London, SE9 2BT, United Kingdom

About this study

Aim:

To analyse and compare the acute effect of two different nitrate formulations on strength and endurance performance in young recreationally trained individuals. In a cross-over within-participant comparison design the participants will be assigned either to ingest (i) 600 mg of Nitrate (N), ii) 600 mg Nitrate and Citrulline (NC) and (iii) Placebo (PL).

Design: Cross-over randomised controlled within participant design including one group undertaking three different treatment conditions.

  • Nitrate (N) providing 600 mg (9.6 mmol) of Nitrate (NO-3).
  • Nitrate + Citrulline (NC) providing 600 mg (9.6 mmol) of Nitrate (NO-3) and 6 g of citrulline-malate.
  • Placebo (PLA) Participants (15 or higher) Inclusion criteria: (a) males and females 18-40 years of age; (b) physically active participants with experience in resistance training performing squat and endurance running as habitual exercises (c) free from musculoskeletal limitations or injuries, (d) agree not to ingest any other supplement during the study.

Exclusion criteria

(a) a history of various metabolic conditions or diseases; (b) use of a variety of medications, including but not limited to those with androgenic and/or anabolic effects and/or nutritional supplements known to affect training outcomes such as creatine, proteins, etc. within 6 weeks before the beginning of the study, (c) current use of tobacco products.

All participants must provide written informed consent by the Declaration of Helsinki. The University ethics committee must approve procedures before starting with the data collection.

Procedures Day 0: Familiarization with the testing procedures including the progressive test to determine the 1RM value in Squat.

Diet Record: Each participant will complete a 1-week diet record using a food frequency questionnaire (FFQ). This questionnaire consists of questions relating to the weekly consumption of different types of food, to estimate energy consumption and the nutritional composition of the reported diets. Participants were instructed to maintain their habitual diet throughout the study. If any change in diet patterns is identified, the participants were dropped from the study.

Supplementation protocol:

Days 1 to 3 Supplements (N, NC, or PLA) will be ingested 2 hr before a standard low-volume training session including 3 sets of 8 to 10 reps of squat and deadlift using a very light load (e.g., own body mass), and flexibility exercises following by 5 min of running at self-paced intensity rated as light (RPE 12). This routine can be completed at home.

Day 4: supplements will be ingested 2.5 hours before the assessments.

The three conditions Nitrate (N) Nitrate + Citrulline (NC) and Placebo (PL) will be tested one week apart, considering a minimum washout period of 72 hours, a strategy that has previously been used in studies with a similar design.

All participants will be following an identical training week in each of the three treatment conditions.

Dependent variables:

o Number of completed repetitions in a singular set to failure in a squat with 75% of 1RM.

Lactate Post (within 1 min of having completed the squat) 15 min rest Progressive to exhaustion on a treadmill (PGT)

  • Ventilatory thresholds (VT1) and (VT2)
  • Vo2 max
  • Lactate post (within 1 min of having completed the PGT)
  • Rating of perceived exertion (RPE) using the Borg 6-to-20-point scale recorded every 2 min and at the end of the PGT.
  • Heart rate associated with VT1, VT2, and Vo2max - Heart rate maximum.
  • Maximal aerobic speed (MAS): calculated from the average speed of the last 2 minutes of the PGT.

15 min rest

  • Maximal Aerobic Speed test (no cortex).
  • Lactate pre (15 min post PGT)
  • The participants should run until exhaustion at the previously determined MAS (e.g. 19.8 km/h)
  • RPE after 1 minute and at the end
  • Heart rate every 1 minute and at the end
  • Lactate post (within 1 minute of having completed the test

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Physically active participants with experience in resistance training performing squats and endurance running as habitual exercises
  • Free from musculoskeletal limitations or injuries
  • Agree not to ingest any other supplement during the study.

Exclusion criteria

  • History of various metabolic conditions or diseases
  • Use of a variety of medications, including but not limited to those with androgenic or anabolic effects or nutritional supplements known to affect training outcomes such as creatine, proteins, etc. within 6 weeks before the beginning of the study
  • Current use of tobacco products.

Treatment and study plan

Nitrate

Dietary Supplement

A four-day supplementation period, separated by one week including a 3-day washout period between conditions will be applied before conducting strength and endurance assessments

Days 1 to 3 the randomly assigned supplement (N, NC, or PLA) will be ingested 2 hr before a standard low-volume training session including 3 sets of 8 to 10 reps of squat and deadlift using a very light load (e.g., own body mass) and flexibility exercises following by 5 min of running at self-paced intensity rated as light (12) with the rating of perceived exertion Borg Scale.

Day 4: the assigned supplement will be ingested 2.5 h before the assessments

Assessment of strength and endurance will be conducted

Other names: Nitrated and citrulline, Placebo

Primary outcomes

  1. Strength

    Time frame: Day 4, 2.5 hours after ingesting the supplement

    Ten maximum repetitions set in back squat using 75% of the previously determined maximal strength determined by the maximum amount of kg lifter in one sigulare repetitions

  2. Maximum oxygen consumption (Vo2max)

    Time frame: through study completion up to 3 weeks

    The highest level of oxygen determined during a progressive to exhaustion running test on a treadmill (PGT)

Secondary outcomes

  1. Ventilatory thresholds (VT1) and (VT2)

    Time frame: 15 minutes after completing the strength test

    ventilatory thresholds using a gas analyser during a progressive to exhaustion running test on a treadmill (PGT)

  2. lactate

    Time frame: through study completion up to 3 weeks

    lactate concentration

  3. Heart Rate

    Time frame: through study completion up to 3 weeks

    Heart Rate response to endurance PGT test

  4. Rate of Perceived Exertion

    Time frame: through study completion up to 3 weeks

    Perception of effort

Other outcomes

  1. Maximal Aerobic Speed

    Time frame: through study completion up to 3 weeks

    the speed at which the Vo2 maximum is determined during the PGT test

Sponsors and collaborators

Lead sponsor

University of Greenwich

Other

Collaborators

  • Crown Sport Nutrition

Registry information

Official study title

Effects of Different Nitrate Formulations on Strength and Endurance Performance in Recreationally Trained Adults

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jul 31, 2024
Registry last updated
Mar 27, 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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