Chronotype Alignment and Time Perception
Circadian Match and Mismatch Effects on Temporal Cognition in Morning- and Evening-Type Adults
1 other identifier
interventional
240
1 country
1
Brief Summary
People differ in chronotype - whether they function best in the morning ("larks") or the evening ("owls"). This study asks whether the match or mismatch between a person's chronotype and the time of day at which they are tested changes how they perceive time. Healthy morning-type and evening-type adults at three sites (Aarhus, Denmark; Changzhou, China; and Hong Kong) complete the same battery of perception and cognition tasks twice - once in the early morning (about 08:00) and once late in the evening (about 22:00), in counterbalanced order. The primary outcome is the accuracy (signed bias) of time-perception judgements; the key comparison is the interaction between chronotype and time of day (the "synchrony effect"). Secondary measures include timing precision, the subjective passage of time, sleepiness, mood, colour perception (with and without blue-blocking glasses) and perceptual decision-making. By testing the same protocol across three cultures and latitudes, the study examines whether circadian match/mismatch effects on temporal cognition generalise across populations.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2025
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2025
CompletedFirst Submitted
Initial submission to the registry
June 22, 2026
CompletedFirst Posted
Study publicly available on registry
June 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2028
June 30, 2026
June 1, 2026
2.8 years
June 22, 2026
June 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Time-perception bias measured by the two-alternative forced-choice duration-comparison point of subjective equality
Participants complete a two-alternative forced-choice duration-comparison task. On each trial, they judge whether a comparison interval is shorter or longer than a standard interval. A psychometric function is fitted to each participant's responses to estimate the point of subjective equality, defined as the comparison duration judged longer than the standard on 50% of trials. Time-perception bias is calculated as signed percentage error: ((point of subjective equality - standard duration) / standard duration) × 100. Positive values indicate a point of subjective equality above the standard duration; negative values indicate a point of subjective equality below the standard duration. The primary comparison is the chronotype-by-session-time interaction, testing whether time-perception bias differs between circadian match and mismatch sessions.
Each of two laboratory sessions, morning about 08:00 and evening about 22:00, completed within about 2 weeks.
Secondary Outcomes (7)
Temporal precision measured by the two-alternative forced-choice duration-discrimination Weber fraction
Each of two laboratory sessions, morning about 08:00 and evening about 22:00, completed within about 2 weeks.
Subjective passage of time measured by a passage-of-time rating scale
Each of two laboratory sessions, morning about 08:00 and evening about 22:00, completed within about 2 weeks.
Subjective sleepiness measured by the Karolinska Sleepiness Scale
Each of two laboratory sessions, morning about 08:00 and evening about 22:00, completed within about 2 weeks.
Mood measured by the Multidimensional Mood Questionnaire
Each of two laboratory sessions, morning about 08:00 and evening about 22:00, completed within about 2 weeks.
Unique-hue settings measured as hue angle in the Commission Internationale de l'Éclairage Colour Appearance Model 2016 (CIECAM16)
Each of two laboratory sessions, morning about 08:00 and evening about 22:00, completed within about 2 weeks.
- +2 more secondary outcomes
Study Arms (2)
Morning-first sequence
EXPERIMENTALParticipants complete the Morning test session (about 08:00) first, then the Evening test session (about 22:00). Both sessions use the identical perception and cognition battery; session order is counterbalanced across participants.
Evening-first sequence
EXPERIMENTALParticipants complete the Evening test session (about 22:00) first, then the Morning test session (about 08:00). Both sessions use the identical perception and cognition battery; session order is counterbalanced across participants.
Interventions
Full perception and cognition battery administered shortly after habitual wake (about 08:00): time-perception tasks (interval production/estimation, duration discrimination, passage-of-time judgement), state measures (sleepiness, mood, arousal), colour tasks, a perceptual conformity task, and a vigilance task.
The identical battery administered late in the evening (about 22:00), enabling within-participant comparison of the same measures at the two times of day.
Eligibility Criteria
You may qualify if:
- Healthy adult, 18-40 years
- Clear morning-type or evening-type on the Morningness-Eveningness Questionnaire (MEQ-SA); intermediate types excluded (state exact cut-offs, e.g. evening-type 41 or below, morning-type 59 or above)
- Normal or corrected-to-normal visual acuity
- Normal colour vision (e.g. Ishihara screening)
- Fluent in the testing-site language (Danish, Chinese, or English)
- Able to attend both an early-morning (about 08:00) and a late-evening (about 22:00) session
You may not qualify if:
- Intermediate chronotype (MEQ in the middle band)
- Night or rotating shift work in the past 3 months, or recent trans-meridian travel (more than 2 time zones in the past 4 weeks)
- Diagnosed sleep disorder (e.g. insomnia, sleep apnoea)
- Current psychiatric or neurological disorder
- Use of sleep medication or psychoactive or CNS-active drugs
- Colour-vision deficiency
- Substance-use disorder
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Child Development Centre
Hong Kong, Hong Kong
Related Publications (6)
Kuriyama K, Uchiyama M, Suzuki H, Tagaya H, Ozaki A, Aritake S, Shibui K, Xin T, Lan L, Kamei Y, Takahashi K. Diurnal fluctuation of time perception under 30-h sustained wakefulness. Neurosci Res. 2005 Oct;53(2):123-8. doi: 10.1016/j.neures.2005.06.006.
PMID: 16039739BACKGROUNDKuriyama K, Uchiyama M, Suzuki H, Tagaya H, Ozaki A, Aritake S, Kamei Y, Nishikawa T, Takahashi K. Circadian fluctuation of time perception in healthy human subjects. Neurosci Res. 2003 May;46(1):23-31. doi: 10.1016/s0168-0102(03)00025-7.
PMID: 12725909BACKGROUNDBuysse DJ, Reynolds CF 3rd, Monk TH, Berman SR, Kupfer DJ. The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research. Psychiatry Res. 1989 May;28(2):193-213. doi: 10.1016/0165-1781(89)90047-4.
PMID: 2748771BACKGROUNDRoenneberg T, Wirz-Justice A, Merrow M. Life between clocks: daily temporal patterns of human chronotypes. J Biol Rhythms. 2003 Feb;18(1):80-90. doi: 10.1177/0748730402239679.
PMID: 12568247BACKGROUNDMay CP, Hasher L. Synchrony effects in inhibitory control over thought and action. J Exp Psychol Hum Percept Perform. 1998 Apr;24(2):363-79. doi: 10.1037//0096-1523.24.2.363.
PMID: 9554091BACKGROUNDHorne JA, Ostberg O. A self-assessment questionnaire to determine morningness-eveningness in human circadian rhythms. Int J Chronobiol. 1976;4(2):97-110.
PMID: 1027738BACKGROUND
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant Professor
Study Record Dates
First Submitted
June 22, 2026
First Posted
June 30, 2026
Study Start
September 1, 2025
Primary Completion (Estimated)
June 30, 2028
Study Completion (Estimated)
June 30, 2028
Last Updated
June 30, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ANALYTIC CODE
- Time Frame
- Beginning after publication of the primary results, with no planned end date.
- Access Criteria
- Open access via the Open Science Framework; no application required.
De-identified individual participant data underlying the published results, together with the study protocol, statistical analysis plan, and analysis code, will be made openly available via the Open Science Framework (OSF).