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Clinical Trials/NCT02952014
NCT02952014
Completed
Not Applicable

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

Texas A&M University1 site in 1 country31 target enrollmentFebruary 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dietary Modification
Sponsor
Texas A&M University
Enrollment
31
Locations
1
Primary Endpoint
Optimize nutrient delivery prior to exercise by assessing Readiness to Perform Visual Analog Scale.
Status
Completed
Last Updated
9 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
February 2014
End Date
May 2014
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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);

Outcomes

Primary Outcomes

Optimize nutrient delivery prior to exercise by assessing Readiness to Perform Visual Analog Scale.

Time Frame: Three weeks

Optimize nutrient delivery prior to exercise by assessing Blood Pressure.

Time Frame: Three weeks

Optimize nutrient delivery prior to exercise by assessing; cognitive function (i.e., Stroop Color and Word Test and Word Recall Test).

Time Frame: Three weeks

Optimize nutrient delivery prior to exercise by assessing Resting Energy Expenditure.

Time Frame: Three weeks

Optimize nutrient delivery prior to exercise by assessing Heart Rate.

Time Frame: Three weeks

Optimize nutrient delivery prior to exercise by assessing ECG.

Time Frame: Three weeks

Secondary Outcomes

  • Measure Heart Rate to evaluate safety.(Three weeks)
  • Measure Blood Pressure to evaluate safety.(Three weeks)
  • Measure standard clinical chemistry panels in the blood to evaluate safety.(Three weeks)
  • Measure ECG to evaluate safety.(Three weeks)

Study Sites (1)

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