- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07671144
Visual Perception, Binocular Competition, and Fatigue-Related Individual Differences in Colour and Illumination Judgement
Characterising Individual Differences in Colour Perception and Binocular Rivalry and Their Associations With Chronotype, Sex, and Sleep
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Colour perception and binocular rivalry both show variability across individuals. However, the extent to which these individual differences are stable and whether they are associated with personal or physiological factors remains unclear. This study will use behavioural visual perception tasks to measure individual differences in colour perception and binocular rivalry. Participants will complete a colour perception task and a binocular rivalry task, along with questionnaire measures related to chronotype, sleep, fatigue, and demographic characteristics including sex.
The primary aim is to determine whether measurable individual differences are present in colour perception and binocular rivalry performance. The secondary aim is to examine whether these differences are associated with chronotype, sex, sleep-related variables, and subjective fatigue. The study is observational and does not involve a clinical intervention, drug, biologic product, or medical device.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Cehao Yu, PhD
- Phone Number: +852 3400 3012
- Email: cehao.yu@polyu.edu.hk
Study Contact Backup
- Name: Junkai Che, Master
- Phone Number: +852 9783 8643
- Email: junkai.che@connect.polyu.hk
Study Locations
-
-
Kowloon
-
Hung Hom, Kowloon, Hong Kong
- The Hong Kong Polytechnic University, Department of Applied Social Sciences
-
Contact:
- Cehao Yu, PhD
- Phone Number: +852 3400 3012
- Email: cehao.yu@polyu.edu.hk
-
Contact:
- Junkai Che, Master
- Phone Number: +852 9783 8643
- Email: junkai.che@connect.polyu.hk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults aged 18 years or older.
- Normal or corrected-to-normal visual acuity.
- Normal or corrected-to-normal binocular vision.
- Normal colour vision, or no self-reported colour vision deficiency.
- Able to understand the study instructions and provide informed consent.
- Able to complete computer-based visual perception tasks and self-report questionnaires.
Exclusion Criteria:
- Self-reported colour vision deficiency.
- Uncorrected visual impairment or eye conditions that may interfere with visual perception tasks.
- Strabismus, amblyopia, or other binocular vision problems that may interfere with binocular rivalry testing.
- History of neurological disorders, photosensitive epilepsy, or severe sensitivity to flickering visual stimuli.
- Current condition or medication that, in the investigator's judgment, may substantially affect visual perception, attention, or task performance.
- Inability to complete the task procedures or provide valid responses.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy Adult Participants
|
Participants will complete computer-based visual perception tasks, including a colour perception task and a binocular rivalry task.
These tasks are used to measure individual differences in perceptual responses and are not intended as a clinical intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Colour perception adjustment metrics
Time Frame: During a single laboratory testing session
|
Colour perception will be measured using a computer-based colour adjustment task.
Participants will adjust the appearance of a target object or stimulus, and outcome variables will include adjustment values in colour space, such as chromaticity, hue, saturation, or luminance-related measures, depending on the final task implementation.
These measures will be used to characterise individual differences in colour perception.
|
During a single laboratory testing session
|
|
Binocular rivalry perception metrics
Time Frame: During a single laboratory testing session
|
Binocular rivalry will be measured using a computer-based visual task in which different images or stimuli are presented separately to the two eyes.
Outcome variables may include perceptual dominance duration, predominance, alternation rate, switch rate, or related behavioural responses.
These measures will be used to characterise individual differences in binocular rivalry perception.
|
During a single laboratory testing session
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Chronotype score
Time Frame: During a single laboratory testing session
|
Chronotype will be assessed using a self-report questionnaire.
The resulting score will be used to examine whether individual differences in colour perception and binocular rivalry are associated with morningness-eveningness preference.
|
During a single laboratory testing session
|
|
Sleep-related measures
Time Frame: Up to 7 days before or around the laboratory testing session
|
Sleep-related variables will be assessed using self-report questionnaire measures, such as recent sleep duration, sleep quality, or sleep timing.
These measures will be used to examine whether sleep-related factors are associated with individual differences in colour perception and binocular rivalry.
|
Up to 7 days before or around the laboratory testing session
|
|
Subjective fatigue
Time Frame: Immediately before and after the visual perception tasks during a single laboratory testing session
|
Subjective fatigue will be assessed using self-report ratings, such as sleepiness or fatigue scales.
These measures will be used to examine whether current fatigue or alertness is associated with colour perception and binocular rivalry measures.
|
Immediately before and after the visual perception tasks during a single laboratory testing session
|
Collaborators and Investigators
Publications and helpful links
General Publications
- Yang E, Blake R, McDonald JE 2nd. A new interocular suppression technique for measuring sensory eye dominance. Invest Ophthalmol Vis Sci. 2010 Jan;51(1):588-93. doi: 10.1167/iovs.08-3076. Epub 2009 Jul 23.
- Webster MA, Miyahara E, Malkoc G, Raker VE. Variations in normal color vision. II. Unique hues. J Opt Soc Am A Opt Image Sci Vis. 2000 Sep;17(9):1545-55. doi: 10.1364/josaa.17.001545.
- Foster DH. Color constancy. Vision Res. 2011 Apr 13;51(7):674-700. doi: 10.1016/j.visres.2010.09.006. Epub 2010 Sep 16.
- Wallisch P. Illumination assumptions account for individual differences in the perceptual interpretation of a profoundly ambiguous stimulus in the color domain: "The dress". J Vis. 2017 Apr 1;17(4):5. doi: 10.1167/17.4.5.
- Gegenfurtner KR, Bloj M, Toscani M. The many colours of 'the dress'. Curr Biol. 2015 Jun 29;25(13):R543-4. doi: 10.1016/j.cub.2015.04.043. Epub 2015 May 14.
- Lafer-Sousa R, Hermann KL, Conway BR. Striking individual differences in color perception uncovered by 'the dress' photograph. Curr Biol. 2015 Jun 29;25(13):R545-6. doi: 10.1016/j.cub.2015.04.053. Epub 2015 May 14.
- Toscani M, Gegenfurtner KR, Doerschner K. Differences in illumination estimation in #thedress. J Vis. 2017 Jan 1;17(1):22. doi: 10.1167/17.1.22.
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HSEARS20260621001 (Other Identifier: The Hong Kong Polytechnic University)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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