Sparrows Farm
Eltham, London, SE9 2BT, United Kingdom
NCT Number: NCT06531070
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)
Looking for future studies?
Notify Me18 year–40 year
All sexes
Interventional
Not applicable
Eltham, London, SE9 2BT, United Kingdom
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.
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)
15 min rest
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
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
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)
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)
Time frame: through study completion up to 3 weeks
lactate concentration
Time frame: through study completion up to 3 weeks
Heart Rate response to endurance PGT test
Time frame: through study completion up to 3 weeks
Perception of effort
Time frame: through study completion up to 3 weeks
the speed at which the Vo2 maximum is determined during the PGT test
University of Greenwich
Other
Effects of Different Nitrate Formulations on Strength and Endurance Performance in Recreationally Trained Adults
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.
Published trials that share one or more normalized conditions with this study.
NCT06602921
Caffeine, Cold Exposure
Loughborough, United Kingdom
View Trial DetailsNCT05143879
Athletes, Citrulline
León, Castille and León, Spain
View Trial DetailsNCT04700241
Brain Insulin-sensitivity, Nitrate
Maastricht, Limburg, Netherlands
View Trial DetailsNCT02115893
Nitrate, Nitrite
Maastricht, Limburg, Netherlands
View Trial Details