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Color Correcting Lenses
Color Correcting Lenses for Color Blindness
N/A
Waitlist Available
Led By Jeffrey Rabin
Research Sponsored by University of the Incarnate Word
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Hereditary color vision deficient (CVDs) verified by failing scores on the red-green anomaloscope (outside system normal range) and Ishihara testing (3 or more errors on 14 testable plates)
No reported history of eye, systemic or ocular disease
Must not have
Reported use of sleep-inducing or wakefulness drugs
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 weeks
Summary
This trial tests special glasses that help people with color vision problems see colors more accurately. It focuses on people who have trouble distinguishing colors. The glasses work by changing how colors look, making it easier for the brain and eyes to tell them apart.
Who is the study for?
This trial is for individuals with hereditary color vision deficiencies (CVDs) who have normal eye health and a visual acuity of at least 20/30. It's also open to those with normal color vision as controls. People using sleep or wakefulness drugs, or those with eye diseases are excluded.
What is being tested?
The study tests if wearing color-correcting lenses can improve the color vision in people with CVDs. Participants will be split into groups; some start with placebo lenses then switch to color-correcting ones, while others do the opposite.
What are the potential side effects?
Since this trial involves non-invasive lenses similar to regular contact lenses, side effects may include discomfort while wearing them, potential eye irritation or strain.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have a confirmed hereditary color vision deficiency.
Select...
I have no history of eye or systemic diseases.
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My vision is at least 20/30 in both eyes.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I use medication to help me sleep or stay awake.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Color Identification Test
Color Matching
Cone Contrast Naming Test
+3 moreTrial Design
5Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: Crossover: Placebo to ExperimentalExperimental Treatment1 Intervention
Placebo Group 1 crosses over to become Experimental Group 2 which includes baseline testing with and without color correcting lenses, followed by 7 days of wear, minimum 3 hours/day, followed by retesting with and without color correcting lenses.
Group II: Color Vision Deficient with Color Correcting LensesExperimental Treatment1 Intervention
10 subjects confirmed to have hereditary color vision deficiency randomly assigned to experimental group 1 which includes baseline testing with and without color correcting lenses, followed by 7 days of wear, minimum 3 hours/day, followed by retesting with and without color correcting lenses.
Group III: Control Group: Subjects with Normal Color VisionActive Control1 Intervention
Fifteen subjects confirmed to have normal color vision will be tested in a single session to determine whether color correcting lenses affect color vision in color vision normal subjects and to provided normative data for several unique measures of color vision performance
Group IV: Crossover: Experimental to PlaceboPlacebo Group1 Intervention
Experimental Group 1 crosses over to become Placebo Group 2 which includes baseline testing with and without placebo lenses, followed by 7 days of wear, minimum 3 hours/day, followed by retesting with and without placebo lenses.
Group V: Color Vision Deficient with Placebo LensesPlacebo Group1 Intervention
10 subjects confirmed to have hereditary color vision deficiency randomly assigned to Placebo Group 1 which includes baseline testing with and without placebo lenses, followed by 7 days of wear, minimum 3 hours/day, followed by retesting with and without placebo lenses.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Placebo Group 1 Crosses over to become Experimental Group 2: Color Correcting Lenses
2022
N/A
~40
Experimental Group 1: Color Correcting Lenses
2022
N/A
~40
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Color blindness treatments primarily aim to enhance color discrimination. One common approach is the use of color-correcting lenses, which alter the wavelengths of light entering the eye.
These lenses work by filtering specific wavelengths to enhance the contrast between colors that color-blind individuals typically struggle to differentiate. This mechanism is crucial for color blindness patients as it can significantly improve their ability to perceive colors more accurately, thereby enhancing their daily functioning and quality of life.
Combined surgery versus cataract surgery alone for eyes with cataract and glaucoma.
Combined surgery versus cataract surgery alone for eyes with cataract and glaucoma.
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Who is running the clinical trial?
University of the Incarnate WordLead Sponsor
17 Previous Clinical Trials
2,450 Total Patients Enrolled
National Eye Institute (NEI)NIH
553 Previous Clinical Trials
1,407,274 Total Patients Enrolled
Jeffrey RabinPrincipal InvestigatorC
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I have a confirmed hereditary color vision deficiency.I use medication to help me sleep or stay awake.I have no history of eye or systemic diseases.My vision is at least 20/30 in both eyes.You can see colors normally, as shown by passing specific color vision tests.
Research Study Groups:
This trial has the following groups:- Group 1: Crossover: Experimental to Placebo
- Group 2: Color Vision Deficient with Color Correcting Lenses
- Group 3: Color Vision Deficient with Placebo Lenses
- Group 4: Crossover: Placebo to Experimental
- Group 5: Control Group: Subjects with Normal Color Vision
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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