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The Effects of a Zeaxanthin Intervention on Visuomotor Function

The Effects of a Zeaxanthin Intervention on Visuomotor Function

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02017418
Enrollment
102
Registered
2013-12-20
Start date
2012-02-29
Completion date
2014-07-31
Last updated
2015-05-27

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

Conditions

Behavior and Behavior Mechanisms

Keywords

zeaxanthin, visual function, reaction time, processing speed

Brief summary

This study was designed to test whether two zeaxanthin formulations (supplements containing different nutritional compounds with zeaxanthin and omega fatty acids being the primary ingredients of interest) influenced visual motor function. Visual motor function refers to the processing speed of the visual system and how individuals respond behavioral to visual stimuli (e.g., reaction time).

Detailed description

This study was designed to test whether two zeaxanthin formulations (supplements containing different nutritional compounds with zeaxanthin and omega fatty acids being the primary ingredients of interest) influenced visual motor function. Visual motor function refers to the processing speed of the visual system and how individuals respond behavioral to visual stimuli (e.g., reaction time).

Interventions

DIETARY_SUPPLEMENTzeaxanthin

softgel

DIETARY_SUPPLEMENTcombinatory supplement

softgel

Sponsors

ZeaVision, LLC
CollaboratorINDUSTRY
University of Georgia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

* Age: ≥18 and ≤ 40 years * BMI: ≥ 20 and ≤ 30 kg/m2 * No anticipated changes in dieting habits (as relevant to the intake of xanthophylls and fats/oils). * No anticipated surgical procedures. * Willingness and ability to give written informed consent and willingness and ability to comply with the study requirements. * Corrected visual acuity (ETDRS): better than 20/60 in the eye selected for the study

Exclusion criteria

* Smokers * Current or history of relevant ocular diseases (such as AMD) or other conditions e.g., lipid disorders. * Inability to reliably perform macular pigment optical density measurements by Heterochromatic Flicker Photometry or any of the other ophthalmic tests of the study. * Any condition likely to interfere with normal gastro-intestinal absorption of xanthophylls (e.g., digestive disorders: inflammatory bowel disease, ulcerative colitis, Crohn's, irritable bowel, etc. or lipid disorders including conditions such as hypercholesterolemia) * Current use of xanthophyll containing supplements or use of xanthophyll containing supplements in the past 6 months (but excluding multivitamins containing lutein or zeaxanthin at low potency). * Participation in any other study during last 1 month before study initiation. * Known hypersensitivity or allergy to xanthophylls. * Regular intake of medications or supplements, which the principal investigator deems likely to confound the study outcomes. These include diabetes medication and statins or any other drug/supplement to modulate cholesterol or fat digestion/absorption.

Design outcomes

Primary

MeasureTime frameDescription
Macular pigment optical densityone yearIncreases in the amount of macular pigment measured in optical density units

Secondary

MeasureTime frameDescription
coincidence anticipation12-monthsbutton press when a light stimulus of varying speeds reaches a specific point in a linear light array
fixed reaction timeone yearreaction time to a stimulus fixed in space
variable reaction time12-monthsreaction time to a stimulus with a position that varies in space

Countries

United States

Outcome results

None listed

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