- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05779228
Visual Mode Switching in Color Perception
January 12, 2026 updated by: University of Minnesota
Participants will be given experience wearing colored lenses that add a tint to the environment.
Changes in visual perception and neural processing that arise as a result of this experience will be measured.
These are expected as participants learn to switch to "colored lenses mode" where the effects of the lenses are discounted and colors appear more normal as soon as the lenses are put on.
Study Overview
Status
Withdrawn
Intervention / Treatment
Detailed Description
All participants will wear tinted lenses for 1 hour at a time, 5 times per day.
Perception (behavior) and neural function (with functional MRI and EEG) before and after this experience will be measured.
In the neural measurements, activity will be recorded while participants view stripes of many different colors both with the lenses on and off.
In the perceptual measurements, participants will adjust the color of a small patch to appear neutral, neither red nor green.
Behavior will be measured in a variety of conditions to test different hypotheses about the origins of the mode-switching effects.
These include: 1) surrounding the patch with different colors, 2) preceding the presentation of the patch with presentation of different colors, 3) presenting the tests in a red-illuminated room, 4) presenting the tests in a completely darkened room, and 5) using a head-mount-display (virtual reality goggles) to present simulated lenses that gradually change in strength.
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Minnesota
-
Minneapolis, Minnesota, United States, 55455
- University of Minnesota
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Normal or corrected to normal vision by contact lenses
- No known visual disorders
- Little to no experience in tinted environments (e.g. dark rooms, swimming goggles)
Exclusion Criteria:
- Abnormal color vision
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Color Contrast
Test patch is surrounded spatially by different colors
|
Wear of colored lenses for 1 hr, 5 times per day, for 5 days
|
|
Experimental: Color Adaptation
Test patch is surrounded temporally (preceded) by different colors
|
Wear of colored lenses for 1 hr, 5 times per day, for 5 days
|
|
Experimental: Neuroimaging
Functional MRI and Electroencephelography data are acquired for multiple test colors
|
Wear of colored lenses for 1 hr, 5 times per day, for 5 days
|
|
Experimental: Red Room
Participants are tested in a red-illuminated room
|
Wear of colored lenses for 1 hr, 5 times per day, for 5 days
|
|
Experimental: Dark Room
Participants are tested in a completely darkened room
|
Wear of colored lenses for 1 hr, 5 times per day, for 5 days
|
|
Experimental: Gradual Change
Participants view a gradual change in tint, presented on a head-mounted display
|
Wear of colored lenses for 1 hr, 5 times per day, for 5 days
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in unique yellow settings
Time Frame: Change will be assessed over the entire study, by comparing a pre-test the day before the intevention (which lasts 5 days) to a post-test the day after the intervention.
|
This is a standard psychophysical measure referenced in 100s of papers.
Participants adjust a patch of color until it appears neither red nor green and this color is reported in standard colorimetric coordinates (e.g.
CIE).
|
Change will be assessed over the entire study, by comparing a pre-test the day before the intevention (which lasts 5 days) to a post-test the day after the intervention.
|
|
Change in BOLD functional MRI activity
Time Frame: Change will be assessed over the entire study, by comparing a pre-test the day before the intevention (which lasts 5 days) to a post-test the day after the intervention.
|
Neural activation will be measured with functional MRI which will be used to measure BOLD activity with standard methods, and reported as percent change from rest, a standard measure, for each voxel in the brain.
|
Change will be assessed over the entire study, by comparing a pre-test the day before the intevention (which lasts 5 days) to a post-test the day after the intervention.
|
|
Change in EEG activity
Time Frame: Change will be assessed over the entire study, by comparing a pre-test the day before the intevention (which lasts 5 days) to a post-test the day after the intervention.
|
Neural activity will be measured with electroencephelography using standard techniques and will be reported as voltage changes over time for each electrode in a standard configuration.
|
Change will be assessed over the entire study, by comparing a pre-test the day before the intevention (which lasts 5 days) to a post-test the day after the intervention.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
January 1, 2026
Primary Completion (Estimated)
February 4, 2031
Study Completion (Estimated)
February 4, 2032
Study Registration Dates
First Submitted
January 20, 2023
First Submitted That Met QC Criteria
March 18, 2023
First Posted (Actual)
March 22, 2023
Study Record Updates
Last Update Posted (Estimated)
January 14, 2026
Last Update Submitted That Met QC Criteria
January 12, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- STUDY00002354
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Completely deidentified data, meta-data, stimulus presentation code, and analysis code will be shared following an NIH data sharing plan.
Data will be shared using the OSF platform, as well as github for code.
IPD Sharing Time Frame
Data will be available for at least 10 years, starting at publication date or end of the study.
IPD Sharing Access Criteria
Publicly accessible
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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