Morning larks vs night owls: does your body clock warp time?
NCT ID NCT07292597
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at how being a 'morning person' or 'night owl' changes the way you experience time. Healthy adults aged 23-45 will do computer tasks at their preferred time of day and again at the opposite time. Researchers want to see if time judgments and alertness are worse when you're out of sync with your natural rhythm.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 128 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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23 to 45 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 23 to 45 years * Able to understand and communicate in Danish * Completed at least upper secondary education (e.g., gymnasium) * Categorized as either a Morning Type (MT) or Evening Type (ET) based on standardized chronotype assessments: * Munich Chronotype Questionnaire (MCTQ): * MT: sleep midpoint on free days (MSFsc) ≤ 03:00 * ET: sleep midpoint on free days (MSFsc) ≥ 05:00 * Morningness-Eveningness Questionnaire (MEQ): * One of four defined chronotype categories (definitely morning, moderately morning, moderately evening, definitely evening). Exclusion Criteria: * Current engagement in shift work, rotating schedules, or other forms of irregular sleep-wake timing * Diagnosis of any neurological, psychiatric, or sleep-related disorder (e.g., insomnia, narcolepsy, sleep apnea) * Use of medications that affect sleep, alertness, or circadian functioning (e.g., melatonin, stimulants, antidepressants) * International travel across time zones within the four weeks preceding study participation * Are classified as having an intermediate chronotype based on validated chronotype assessments (MCTQ or MEQ), as this group does not provide the necessary contrast to evaluate circadian alignment effects.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Cognition and Behavior Lab
RECRUITINGAarhus, 8000, Denmark
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Other studies related to the condition(s) this trial covers.
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