NCT05779228

Brief Summary

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.

Trial Health

50
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
70mo left

Started Jan 2026

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress6%
Jan 2026Feb 2032

First Submitted

Initial submission to the registry

January 20, 2023

Completed
2 months until next milestone

First Posted

Study publicly available on registry

March 22, 2023

Completed
2.8 years until next milestone

Study Start

First participant enrolled

January 1, 2026

Completed
5.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 4, 2031

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

February 4, 2032

Last Updated

January 14, 2026

Status Verified

January 1, 2026

Enrollment Period

5.1 years

First QC Date

January 20, 2023

Last Update Submit

January 12, 2026

Conditions

Keywords

Visual PerceptionVisual AdaptationColor Perception

Outcome Measures

Primary Outcomes (3)

  • Change in unique yellow settings

    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

    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

    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.

Study Arms (6)

Color Contrast

EXPERIMENTAL

Test patch is surrounded spatially by different colors

Behavioral: Mode Switching Training

Color Adaptation

EXPERIMENTAL

Test patch is surrounded temporally (preceded) by different colors

Behavioral: Mode Switching Training

Neuroimaging

EXPERIMENTAL

Functional MRI and Electroencephelography data are acquired for multiple test colors

Behavioral: Mode Switching Training

Red Room

EXPERIMENTAL

Participants are tested in a red-illuminated room

Behavioral: Mode Switching Training

Dark Room

EXPERIMENTAL

Participants are tested in a completely darkened room

Behavioral: Mode Switching Training

Gradual Change

EXPERIMENTAL

Participants view a gradual change in tint, presented on a head-mounted display

Behavioral: Mode Switching Training

Interventions

Wear of colored lenses for 1 hr, 5 times per day, for 5 days

Color AdaptationColor ContrastDark RoomGradual ChangeNeuroimagingRed Room

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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)

You may not qualify if:

  • Abnormal color vision

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Minnesota

Minneapolis, Minnesota, 55455, United States

Location

Related Publications (1)

  • Li Y, Tregillus KE, Luo Q, Engel SA. Visual mode switching learned through repeated adaptation to color. Elife. 2020 Dec 15;9:e61179. doi: 10.7554/eLife.61179.

0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: The interventional study type is correct. The investigative team is giving all subjects a treatment- behavioral training in visual mode switching- and measuring effects of that treatment, by comparing measures made before to measures made after the treatment. Thus, this is a within-subjects, repeated measures experimental design. The experimenters have 6 different measurements they are using this design in different groups of subjects run in parallel, all examining different effects of the same treatment. . This is why parallel study model is appropriate. These parallel groups with different measurements, but same treatment, are the arms of the study.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 20, 2023

First Posted

March 22, 2023

Study Start

January 1, 2026

Primary Completion (Estimated)

February 4, 2031

Study Completion (Estimated)

February 4, 2032

Last Updated

January 14, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will share

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.

Shared Documents
STUDY PROTOCOL, ANALYTIC CODE
Time Frame
Data will be available for at least 10 years, starting at publication date or end of the study.
Access Criteria
Publicly accessible
More information

Locations