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Assessment of a Pre-Workout Dietary Supplement

Pharmacokinetic, Thermogenic, Hemodynamic, Ergogenic Assessment of a Pre-Workout Dietary Supplement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02952014
Acronym
NB1
Enrollment
31
Registered
2016-11-02
Start date
2014-02-28
Completion date
2014-05-31
Last updated
2016-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dietary Modification

Brief summary

The purpose of this study is to examine the acute effects of a pre-workout dietary supplement on energy metabolism, cardiovascular hemodynamics, blood metabolites and mental focus.

Detailed description

A number of nutritional strategies have been developed to optimize nutrient delivery prior to exercise. This includes providing carbohydrate and a number of ergogenic nutrients prior to, during and/or following exercise. As a result a number of pre-workout supplements have been developed to increase energy availability, promote vasodilation and/or positively affect exercise capacity. The purpose of this study is to investigate the potential ergogenic value of acute ingestion of a pre-workout dietary supplement prior to exercise.

Interventions

DIETARY_SUPPLEMENTC4 Extreme

Pre-Workout Dietary Supplement

DIETARY_SUPPLEMENTC4 Extreme (without Advantra Z

Pre-Workout Dietary Supplement

DIETARY_SUPPLEMENTPlacebo

Pre-Workout Dietary Supplement

Sponsors

Nutrabolt
CollaboratorINDUSTRY
Texas A&M University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* you are an apparently healthy and recreationally active man or woman between the ages of 18 and 40; * you will need to have at least six months immediate prior history of resistance training on the bench press and leg press or squat;

Exclusion criteria

* you have a history of treatment for metabolic disease (i.e., diabetes), hypertension, hypo-tension, thyroid disease, arrhythmia and/or cardiovascular disease; * you are currently using prescription medications; * you have an intolerance to caffeine and/or other natural stimulants; * you are pregnant or a lactating female or plan to become pregnant with the next month; * you have a history of smoking; * you drink excessively (i.e., 12 drinks per week or more);

Design outcomes

Primary

MeasureTime frame
Optimize nutrient delivery prior to exercise by assessing ECG.Three weeks
Optimize nutrient delivery prior to exercise by assessing Readiness to Perform Visual Analog Scale.Three weeks
Optimize nutrient delivery prior to exercise by assessing Resting Energy Expenditure.Three weeks
Optimize nutrient delivery prior to exercise by assessing Heart Rate.Three weeks
Optimize nutrient delivery prior to exercise by assessing Blood Pressure.Three weeks
Optimize nutrient delivery prior to exercise by assessing; cognitive function (i.e., Stroop Color and Word Test and Word Recall Test).Three weeks

Secondary

MeasureTime frame
Measure Heart Rate to evaluate safety.Three weeks
Measure Blood Pressure to evaluate safety.Three weeks
Measure ECG to evaluate safety.Three weeks
Measure standard clinical chemistry panels in the blood to evaluate safety.Three weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026