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NCT04539054 · ClinicalTrials.gov registry record · NA

Pre-workout Supplement Versus Caffeine on Energy Expenditure.

A NA study, sponsored by Northern Illinois University.

Completed
Registry status
NA
Development phase
12
Enrollment target

NCT04539054 is a NA study that has completed, run by Northern Illinois University. The registered enrollment target is 12 participants.

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The verdict

NCT04539054, a NA study, has completed, sponsored by Northern Illinois University.

COMPLETED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

The primary purpose of this study was to examine the acute effects of a multi-ingredient pre-workout supplement versus an ergogenic dose of caffeine (6 mg/kg) on energy expenditure during low-intensity exercise. The effects of these substances on substrate utilization, gas exchange, and psychological factors were also investigated. Twelve males (mean ± SD: age = 22.8 ± 2.4 years) completed three bouts of 60-min of treadmill exercise at 4.8-6.4 km/hr on separate days after consuming a pre-workout supplement, 6 mg/kg of caffeine, or placebo in a randomized fashion. The pre-workout and caffeine supplements resulted in significantly greater energy expenditure (p \< 0.001, p = 0.006, respectively), VO2 (p \< 0.001, p = 0.007, respectively), VCO2 (p = 0.006, p = 0.049, respectively), and VE (p \< 0.001, p = 0.007, respectively), but not rates of fat or carbohydrate oxidation or respiratory exchange ratio compared to placebo (collapsed across condition). In addition, the pre-workout supplement increased feelings of alertness (p = 0.015) and focus (p = 0.005) 30-minutes post-ingestion and decreased feelings of fatigue (p = 0.014) during exercise compared to placebo (collapsed across condition). Thus, the pre-workout supplement increased energy expenditure and measures of gas exchange to the same extent as 6 mg/kg of caffeine with concomitant increased feelings of alertness and focus and decreased feelings of fatigue.

Interventions

  • DIETARY_SUPPLEMENT ENGN Shred
  • DIETARY_SUPPLEMENT Nutricost caffeine powder
  • DIETARY_SUPPLEMENT Crystal Light

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2019-09-01
Est. Completion 2019-12-31
Phase NA

Sponsor

Northern Illinois University

5 total trials

What the Registry Record Tells You About NCT04539054

The ClinicalTrials.gov registry entry for NCT04539054 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northern Illinois University, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which ENGN Shred is the first listed.

NCT04539054 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04539054 about?

NCT04539054 is a clinical study titled "Pre-workout Supplement Versus Caffeine on Energy Expenditure.". The primary purpose of this study was to examine the acute effects of a multi-ingredient pre-workout supplement versus an ergogenic dose of caffeine (6 mg/kg) on energy expenditure during low-intensity exercise. The effects of these substances on substrate utilization, gas exchange, and psychologica...

What is the current status of trial NCT04539054?

This trial is currently completed. It is a NA study. The enrollment target is 12 participants. The study started on 2019-09-01. Estimated completion is 2019-12-31.

What interventions are being tested in trial NCT04539054?

The interventions under investigation include: ENGN Shred (DIETARY_SUPPLEMENT), Nutricost caffeine powder (DIETARY_SUPPLEMENT), Crystal Light (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT04539054?

This trial is sponsored by Northern Illinois University, which has 5 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.