Clinical Trials Directory

Trials / Completed

CompletedNCT02734251

Effect of Relora Supplement on Anxiety, Cognitive Performance & Mood Tested After Induced Stress

Effects of Magnolia and Phellodendron (Magnolia Officinalis and Phellodendron Amurense) Bark Extracts on Anxiety, Cognitive Performance, and Mood Tested After Induced Stress

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
36 (actual)
Sponsor
InterHealth Nutraceuticals, Inc. · Industry
Sex
All
Age
21 Years – 59 Years
Healthy volunteers
Accepted

Summary

The present randomized, double-blind, placebo-controlled crossover trial aims to evaluate the effects of Relora supplementation on responses to induced stress produced by a combination of cognitive and physiologic stressors in healthy men and women. The effects of the supplement, compared with a placebo, will be evaluated using measures to assess anxiety \[State-Trait Anxiety Inventory-Part 1 (STAI-Part 1), mood \[Bond-Lader Visual Analog Scale (VAS)\], hypothalamic-pituitary-adrenal axis activation (salivary cortisol) and cognitive function (cognitive flexibility, reaction time, processing speed, attention, sustained attention, working memory, and executive function). Testing will be completed at the beginning and end of 7-d supplementation periods with the active and placebo products to assess both the acute effects and the "acute-on-chronic" effects following one week of daily use.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTRelora750 mg/day
DIETARY_SUPPLEMENTPlacebo

Timeline

Start date
2016-02-01
Primary completion
2016-05-01
First posted
2016-04-12
Last updated
2016-05-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02734251. Inclusion in this directory is not an endorsement.