VisionPure Dietary Supplement for Eye Health

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Applied Science and Performance Institute, Tampa, FL
Eye Health+2 More
VisionPure Dietary Supplement - DietarySupplement
Eligibility
18 - 65
All Sexes
What conditions do you have?
Select

Study Summary

VisionPure™ is a softgel dietary supplement containing fish oil, lutein, zeaxanthin, and vitamin D. The intent of the VisionPure product is to assist in maintaining eye and cognitive health while helping to provide protection against blue throughout the day. In this pilot trial, approximately 16 participants will be recruited and randomly assigned to experimental and placebo conditions. Participants will consume 1 serving (2 softgels) per day of their respective study condition for 60 days. Prior to and following the 60 day supplementation period, participants will undergo a series of optometry and cognitive examinations to quantify eye health and cognitive function outcomes.

Eligible Conditions

  • Eye Health
  • Cognitive Functioning
  • Vision

Treatment Effectiveness

Study Objectives

3 Primary · 6 Secondary · Reporting Duration: Day 0, Day 60

Day 0, Day 60
Change in Central Retinal Thickness
Change in Cognitive Attention
Change in Color Vision
Change in Composite Memory
Change in Ganglion Cell Complex Thickness
Change in Intraocular Pressure
Change in Verbal Memory
Change in Visual Acuity
Change in Visual Memory
Changes in National Eye Institute Visual Functioning Questionnaire - 25 (VFQ-25)

Trial Safety

Trial Design

2 Treatment Groups

VisionPure Dietary Supplement
1 of 2
Placebo
1 of 2
Experimental Treatment
Non-Treatment Group

16 Total Participants · 2 Treatment Groups

Primary Treatment: VisionPure Dietary Supplement · Has Placebo Group · N/A

VisionPure Dietary Supplement
DietarySupplement
Experimental Group · 1 Intervention: VisionPure Dietary Supplement · Intervention Types: DietarySupplement
Placebo
DietarySupplement
PlaceboComparator Group · 1 Intervention: Placebo · Intervention Types: DietarySupplement

Trial Logistics

Trial Timeline

Approximate Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: day 0, day 60
Closest Location: Applied Science and Performance Institute · Tampa, FL
Photo of Tampa  1Photo of Tampa  2Photo of Tampa  3
2022First Recorded Clinical Trial
1 TrialsResearching Eye Health
1 CompletedClinical Trials

Eligibility Criteria

Age 18 - 65 · All Participants · 4 Total Inclusion Criteria

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About The Reviewer

Michael Gill preview

Michael Gill - B. Sc.

First Published: October 9th, 2021

Last Reviewed: August 12th, 2022

Michael Gill holds a Bachelors of Science in Integrated Science and Mathematics from McMaster University. During his degree he devoted considerable time modeling the pharmacodynamics of promising drug candidates. Since then, he has leveraged this knowledge of the investigational new drug ecosystem to help his father navigate clinical trials for multiple myeloma, an experience which prompted him to co-found Power Life Sciences: a company that helps patients access randomized controlled trials.