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Consumption of 4D Dietary Supplement on Perceptual-Cognitive and Visual-Motor Performance

Acute Consumption of 4D Dietary Supplement vs. Placebo: Effects on Perceptual-Cognitive and Visual-Motor Performance

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04988919
Enrollment
24
Registered
2021-08-04
Start date
2021-07-26
Completion date
2021-10-04
Last updated
2021-10-08

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

Conditions

Dietary Supplementation

Keywords

multi-ingredient supplement, reaction time, reactive agility, cognition

Brief summary

The purpose of this investigation is to determine if supplementation with the 4D dietary supplement impacts perceptual-cognitive and visual-motor skills in healthy individuals.

Detailed description

Multi-ingredient supplements (MIS) have been reported to positively impact various aspects of performance. While caffeine alone has been shown to improve aerobic performance, resistance training (such as bench press), reaction time and sprint performance, it has also been suggested that it lacks the ability to improve cognition. Therefore, the purpose of this investigation is to examine the effects of a caffeine containing MIS on measures of cognition and reaction time, with the intent of providing additional benefits to athletic performance. This study will utilize a randomized, double-blind, placebo-controlled design. Following two familiarization trials, participants will complete two testing visits. During these visits, they will complete baseline assessments, consume either the 4D dietary supplement or a taste matched placebo, and rest for 45 minutes. Reaction time, cognition assessments (visual tracking speed), and reactive agility performance will be assessed following the rest period.

Interventions

DIETARY_SUPPLEMENT4D

multi-ingredient supplement mixed with 24 ounces of water

DIETARY_SUPPLEMENTplacebo

taste-matched placebo mixed with 24 ounces of water

Sponsors

4D, LLC
CollaboratorUNKNOWN
University of Central Florida
Lead SponsorOTHER

Study design

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

Masking description

All investigators and participants will be blinded to the treatment groups.

Intervention model description

Participants will consume the 4D dietary supplement and the placebo in a randomized order on different testing days. Both the supplement and the placebo will be mixed with 24 fluid ounces of water. All drinks will have a similar appearance and taste. Researchers and participants will be blinded to the contents.

Eligibility

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

Inclusion criteria

* Male or female between the ages of 18-40 years old * Determined to be healthy by the MHQ and PAR-Q+

Exclusion criteria

* Any response of yes on the PAR-Q+ * Daily caffeine consumption greater than 200 mg

Design outcomes

Primary

MeasureTime frameDescription
Change in visual tracking speed in response to supplement/placebo consumptionpre and post supplement ingestion on both testing days (Day 3 and Day 4)Determined via multiple object tracking test on the Neurotracker
Change in reactive agility timepost supplement ingestion on both testing days (Day 3 and Day 4)Determined via Y-Reactive Agility test using the Witty Wireless Timing Gate system
Change in reaction time in response to supplement/placebo consumptionpre and post supplement ingestion on both testing days (Day 3 and Day 4)Determined via Dynavision D2, Mode A

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026