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The Effects of VisionPure™ on Indices of Vision Health and Cognitive Function

The Effects of VisionPure™ on Indices of Vision Health and Cognitive Function: A Randomized, Double-Blind, Placebo-Controlled, Parallel Pilot Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05533658
Enrollment
15
Registered
2022-09-09
Start date
2022-08-01
Completion date
2023-02-03
Last updated
2023-05-26

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

Conditions

Cognitive Function, Eye Health, Vision

Keywords

Fish Oil, Vitamin D, Antioxidant, Eye Health, Cognitive Function, Vision Health

Brief 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.

Detailed description

The study design is a randomized, double-blind, placebo-controlled, parallel design, pilot trial. 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. All study-related procedures will be carried out at 2 locations, The Applied Science and Performance Institute, as well as at True Eye Experts. Both locations are in Tampa, FL. All screening for the study and the signing of all IRB documents will be held at the Applied Science and Performance Institute. Optometry eye examination at Day 0 and Day 60 will be conducted under the supervision of a board-certified O.D. at the True Eye Experts location. Computer-based cognitive assessments using a program called CNS Vital Signs will be carried out at Day 0 and Day 60 at the Applied Science and Performance Institute. The following exams will be carried out: Verbal Memory, Visual Memory, Composite Memory, and Cognitive Attention.

Interventions

DIETARY_SUPPLEMENTVisionPure Dietary Supplement

Subjects will consume two softgels capsules of the Treatment (VisionPure) once daily for 60 days. At Day 0, they will come in for a Comprehensive Eye Exam, a National Eye Institute Visual Functioning Questionnaire, and a series of Cognitive Function Exams. After 60 days, subjects will return and repeat the same questionnaires and exams from Day 0.

DIETARY_SUPPLEMENTPlacebo

Subjects will orally consume two softgel capsules of Placebo once daily for 60 days. At Day 0, they will come in for a Comprehensive Eye Exam, a National Eye Institute Visual Functioning Questionnaire, and a series of Cognitive Function Exams. After 60 days, subjects will return and repeat the same questionnaires and exams from Day 0.

Sponsors

True Eye Experts - New Tampa
CollaboratorUNKNOWN
Applied Science & Performance Institute
Lead SponsorINDUSTRY

Study design

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

Eligibility

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

Inclusion criteria

* Male or female * Age 18-40 years * English literate * Willing to sign informed consent form

Exclusion criteria

* Current cataracts or prior cataract extraction * Glaucoma * Uveitis * Macular hole or traction * Retinitis pigmentosa * Significant epiretinal membrane * Dry eye syndrome of any form * LASIK procedure * Diagnosed concussion within the last 6 months * Optic neuropathy * Neurological disease * Metabolic disease * Cardiovascular disease * Renal disease * History of previous ocular surgery, trauma, intraocular injections or photocoagulation * Vitamin D3, omega fatty acids, or fish oil supplementation with the last 6 months

Design outcomes

Primary

MeasureTime frameDescription
Change in Intraocular PressureDay 0, Day 60Diagnostic Procedure: Retinal Optical Coherence Tomography
Change in Ganglion Cell Complex ThicknessDay 0, Day 60Diagnostic Procedure: Retinal Optical Coherence Tomography
Change in Central Retinal ThicknessDay 0, Day 60Diagnostic Procedure: Retinal Optical Coherence Tomography

Secondary

MeasureTime frameDescription
Change in Verbal MemoryDay 0, Day 60How well can an individual recognize, remember, and recall words.
Change in Visual MemoryDay 0, Day 60How well can in individual recognize, remember, and recall a combination of words and images.
Change in Cognitive AttentionDay 0, Day 60The ability to handle multiple tasks at once and shift attention.
Change in Composite MemoryDay 0, Day 60How well an individual can recognize, remember, and recall a combination of words and images.
Change in Visual AcuityDay 0, Day 60Determines the clarity of your distance vision according to the Snellen Chart.
Change in Color VisionDay 0, Day 60Determines the normality of or defectiveness of color vision. Reference Range: 1 to 11 according to Ishihara Plates (\>10 is normal, 7 or \<7 is deficient).

Other

MeasureTime frameDescription
Changes in National Eye Institute Visual Functioning Questionnaire - 25 (VFQ-25)Day 0, Day 60Subjective/Self-Reported Eye Health Questionnaire.

Countries

United States

Outcome results

None listed

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