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Healthy Adult MaleNCT07217210

Multi-Ingredient Preworkout Supplement on Peak Torque and Muscle Activation During Fatigue

A study testing Multi-ingredient preworkout supplement in people with Healthy Adult Male, run by Northern Illinois University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The primary purpose of the present study was to examine the acute effects of a MIPS product on peak torque production of the leg extensors during a fatiguing isokinetic protocol involving isometric, concentric, and eccentric muscle actions. Read more about this study

Who is it for?
Ages 19 to 29 years, men onlyHealthy volunteers can take part
Conditions the study is for
Healthy Adult Male
What is being tested?
Multi-ingredient preworkout supplement
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
13 participants
Where
1 siteUnited States
Study dates
15 Nov 2021to 1 Apr 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 19 to 29 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Male, 19-29 years of age, one year of resistance training experience

Who cannot join

  • Subjects were eligible to participate if they did not report: 1) cardiovascular disease, metabolic, renal, hepatic, or musculoskeletal disorders; 2) use of any medications; 3) use of nutritional supplements; 4) habitual use of caffeine (≥ 1 caffeinated beverage per day); or 5) participation in another clinical trial or investigation of another nutritional product within 30 days of screening/enrollment.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Northern Illinois University

    DeKalb, Illinois, 60115

Other trials in United States

About this study

Official title: Acute Effects of a Multi-Ingredient Preworkout Supplement on Peak Torque and Muscle Activation During an Isokinetic Fatigue Protocol

The primary purpose of the present study was to examine the acute effects of a MIPS product on peak torque production of the leg extensors during a fatiguing isokinetic protocol involving isometric, concentric, and eccentric muscle actions. In addition, we investigated the effects of the MIPS supplement on EMG amplitude and median power frequency (MDF) responses from the vastus lateralis, rectus femoris, and vastus medi-alis muscles.

Read the detailed description

In the past several years, the use of multi-ingredient pre-workout supplements (MIPS) has become extremely popularized, and their ergogenic potential has become well-established for various sports and within the general population by both competi-tive and recreational athletes [1-6]. Some of the more prevalent ingredients in MIPS in-clude caffeine, β-alanine, L-citrulline, L-arginine, and creatine, with many of these in-gredients and others often combined into proprietary blends [7]. Although recent find-ings indicate synergistic effects among these ingredients may be present [8], it has been suggested that caffeine is the predominant factor responsible for the acute ergogenic effects associated with MIPS [2,9]. In fact, the recommended timing for ingestion of most MIPS is likely based on the stimulating effects of caffeine which typically peaks in the bloodstream 30-60 minutes post-ingestion [10,11]. As a nutritional supplement, caffeine has been shown to be beneficial for maintaining maximal strength and endur-ance as well as improving time-trial performance and other forms of high-intensity ex-ercise [10,11]. These effects have been attributed to improved motor unit firing rates and calcium release from the sarcoplasmic reticulum, subsequently enhancing muscle contraction force [4,12]. β-alanine is another ingredient included in most MIPS [7] and has been identified as the rate-limiting precursor to carnosine, an intracellular muscle buffer [13]. Supplementation with β-alanine has been shown to increase intramuscular levels of carnosine, thereby attenuating metabolic acidosis during high-intensity exer-cise [13]. As precursors to the potent vasodilator, nitric oxide, both L-citrulline and L-arginine supplements have been demonstrated to enhance blood flow to active mus-cles, subsequently delaying the onset of muscular fatigue [14-16]. Based on these collec-tive physiological mechanisms, a MIPS containing these notable ergogenic ingredients (caffeine, β-alanine, L-citrulline, L-arginine) may provide neuromuscular benefits for sustaining force or power output during various forms of vigorous activity.

The vast majority of previous investigations examining the acute effects of MIPS on performance have focused on isotonic variables of upper and lower body muscular strength [i.e. bench press, leg press, and squat one-repetition maximum (1-RM), maxi-mum voluntary contractions (MVC)], endurance (i.e. repetitions to failure at %1-RM), and power (vertical jump, Wingate Anaerobic testing, and critical power) [1-6,9,12,18,19]. Despite conflicting evidence for maximal force and power production [4,6,20,21], the findings of several studies [1,3,4,12,17-19,22,23] have largely indicated acute MIPS supplementation can enhance overall force retention and muscular endur-ance during prolonged or intermittent bouts of high intensity activity. Currently, how-ever, the exact underlying mechanisms responsible for these benefits on neuromuscular function are poorly understood.

Isokinetic dynamometers coupled with surface electromyography (EMG) record-ings are two frequently utilized instruments for the non-invasive assessment of neu-romuscular function and fatigue during static and dynamic muscle actions [24-27]. The utility of isokinetic testing involves the ability to measure isometric, concentric, and eccentric torque levels across an entire range of motion at controlled velocities with minimal skill involvement required. Results from isokinetic testing can provide torque production at different joint angles, while identifying muscle imbalances, tracking the recovery process from injury or surgery, and measuring the rate of force development [28,29]. Thus, as both a training and assessment tool, isokinetic testing is common in clinical and performance settings.

Surface electromyography (EMG) is a technique that involves recording and quantifying the action potentials associated with contracting skeletal muscle fibers [30]. The amplitude contents of the EMG signal reflect the level of muscle activation (i.e. motor unit recruitment and firing rates) [31], whereas the frequency contents pro-vide information related to the muscle fiber conduction velocity [32]. To our knowledge, only one study [5] has directly examined EMG responses associated with acute MIPS administration. Specifically, Negro et al. [5] reported acute MIPS (creatine, arginine, β-alanine, glutamine, taurine) ingestion improved EMG-based indicators of fatigue (i.e. conduction velocity, fractal dimension) during sustained isometric contrac-tions following a resistance exercise protocol designed to elicit fatigue. The authors [5] proposed these acute benefits of their MIPS product may be attributable to improved: 1) peripheral components of performance fatiguability, 2) buffering capacity of the mus-cle from β-alanine, and 3) regulation of mechanisms associated with exercise-induced fatigue from arginine, glutamine, and taurine. Based on these findings [5], valuable in-sight can be gained into the underlying neuromuscular factors associated with MIPS ingestion by examining muscle function and fatigue through isokinetic and EMG as-sessments. Thus, the primary purpose of the present study was to examine the acute ef-fects of a MIPS product on peak torque production of the leg extensors during a fatigu-ing isokinetic protocol involving isometric, concentric, and eccentric muscle actions. In addition, we investigated the effects of the MIPS supplement on EMG amplitude and median power frequency (MDF) responses from the vastus lateralis, rectus femoris, and vastus medialis muscles.

Being tested
Multi-ingredient preworkout supplement
Keywords
isometric; concentric; eccentric; leg extensors; quadriceps; electromyography

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Multi-ingredient preworkout supplementDietary supplement

    Experimental supplement.

Study groups in NCT07217210
Study groupRoleWhat they receive
Supplement groupExperimentalMulti-ingredient preworkout supplement
Receives: Dietary Supplement: Multi-ingredient preworkout supplement
Placebo groupPlacebo comparatorMicrocystalline cellulose
Receives: Dietary Supplement: Multi-ingredient preworkout supplement

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Peak torque

    Isometric, concentric, and eccentric.

    Measured: Two days.

Secondary outcomes (1)
  1. EMG responses.

    Relative amplitude and median power frequency.

    Measured: 60 minutes per visit over the course of two visits (each separated by one week).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Oct 2025
  2. Study start15 Nov 2021
  3. Primary completion1 Mar 2022
  4. Study completion1 Apr 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Crossover
Model description
Within-subjects, placebo-controlled, crossover design
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
13 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07217210
Sponsor's protocol ID
#HS22-0139
Status last verified
Oct 2025
First submitted
13 Oct 2025
Last updated
15 Oct 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The informed consent and IRB application indicated that individual data would not be shared.

Questions about this trial

What is this clinical trial studying?

A study testing Multi-ingredient preworkout supplement in people with Healthy Adult Male, run by Northern Illinois University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Peak torque (time frame: Two days.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Oct 2025.

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