Clinical Trials Directory

Trials / Completed

CompletedNCT04895800

An Evaluation of the Effects of a Non-Caffeinated Energy Dietary Supplement

An Evaluation of the Effects of a Non-Caffeinated Energy Die-tary Supplement on Cognitive and Physical Performance: A Randomized Double-Blind Placebo-Controlled Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
36 (actual)
Sponsor
Nova Southeastern University · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

This study tested the effects of a botanical blend to a caffeine and a placebo condition on 1) self-reported alertness, anxiety, and headaches 2) multiple measures of attention 3) physical performance and 4) stress biomarkers.

Detailed description

This study aimed to build on this work by investigating the possibility that a specific botanical blend (Phytovive™); comprised of Bacopa monnieri bacosides, Kaempferia parviflora methoxy flavones, pomegranate peel polyphenols, and Moringa oleifera leaf saponins) could improve cognitive and physical performance. To this end, this study was a randomized, double-blind, placebo-controlled 21-day parallel study on 36 healthy adults. The study compared the effects of the botanical blend at baseline to a caffeine and a placebo condition on 1) self-reported alertness, anxiety, and headaches 2) multiple measures of attention 3) physical performance and 4) stress biomarkers.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPhytoviveBacopa monnieri bacosides, Kaempferia parviflora methoxy flavones, pomegranate peel polyphenols, and Moringa oleifera leaf saponins)
DIETARY_SUPPLEMENTPlaceboNatural Flavors \[Chocolate, Caramel, Vanilla Cream\], Silica, Inulin, Sucralose)
DIETARY_SUPPLEMENTCaffeineCaffeine (Green tea caffeine extract (170 mg; to deliver 34 mg caffeine \[20% natural caf-feine\])

Timeline

Start date
2020-01-03
Primary completion
2021-01-20
Completion
2021-03-15
First posted
2021-05-20
Last updated
2021-06-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04895800. Inclusion in this directory is not an endorsement.