Visual Perception, Binocular Competition, and Fatigue-Related Individual Differences in Colour and Illumination Judgement

June 22, 2026 updated by: Dr YU Cehao, The Hong Kong Polytechnic University

Characterising Individual Differences in Colour Perception and Binocular Rivalry and Their Associations With Chronotype, Sex, and Sleep

This observational study aims to characterise individual differences in colour perception and binocular rivalry. Participants will complete computer-based visual perception tasks, including a colour perception task and a binocular rivalry task. The study will first examine whether individuals show measurable differences in these perceptual responses. It will then explore whether these differences are associated with chronotype, sex, sleep-related measures, and subjective fatigue. The findings may help clarify how stable individual characteristics and daily physiological states relate to visual perception.

Study Overview

Status

Not yet recruiting

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

Observational

Enrollment (Estimated)

128

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Kowloon
      • Hung Hom, Kowloon, Hong Kong
        • The Hong Kong Polytechnic University, Department of Applied Social Sciences
        • Contact:
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Healthy adult volunteers will be recruited from the university community and/or the surrounding community. Participants will complete computer-based colour perception and binocular rivalry tasks, together with self-report measures of chronotype, sleep, fatigue, and demographic characteristics.

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

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

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

This is where you will find people and organizations involved with this study.

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)

July 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

June 22, 2026

First Submitted That Met QC Criteria

June 22, 2026

First Posted (Actual)

June 26, 2026

Study Record Updates

Last Update Posted (Actual)

June 26, 2026

Last Update Submitted That Met QC Criteria

June 22, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

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)?

UNDECIDED

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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