Circadian Rhythms, Sleep, Time Perception
Conditions
Keywords
circadian phase delay, Healthy adults
Brief summary
The purpose of this study is to investigate whether the experience of a daily time delay can affect our internal circadian rhythm.
Interventions
All activities occur at the same time every day
All activities will be delayed by one hour per day over a 5 day period.
Sponsors
Study design
Masking description
Open-label, single-group basic science study; no masking used.
Intervention model description
Participating couples will need to live in this environment for 5 consecutive days. By lottery draw, you as a couple will either be exposed to a fixed daily routine, where all activities occur at the same time every day, or a daily time delay of 1 hour, where all activities will be delayed by one hour.
Eligibility
Inclusion criteria
* Healthy adults aged 23-45 years * Part of a heterosexual, cohabiting couple willing to participate together in a five-day in-laboratory study * Both partners meet all inclusion criteria * Completion of at least upper-secondary education * Maintain a regular sleep-wake schedule * Habitual sleep timing within a normative range (non-extreme chronotype), assessed using the Morningness-Eveningness Questionnaire (MEQ) or the Munich Chronotype Questionnaire (MCTQ) * Both partners fall within the acceptable chronotype range to ensure aligned sleep-wake patterns * Low seasonality scores on the Seasonal Pattern Assessment Questionnaire (SPAQ) * Free from underlying sleep or mood disorders
Exclusion criteria
* Engages in night-shift work or maintains an irregular work or sleep schedule * International travel involving a time-zone change of more than two hours within the past two months, or anticipated travel before study completion * Diagnosed neurological, psychiatric, or sleep disorder (e.g., insomnia, sleep apnea, bipolar disorder) * High risk of sleep apnea, defined as a Berlin Questionnaire score \>2 (Lauritzen et al., 2018) * Use of medications known to affect sleep, alertness, melatonin secretion, or circadian timing * Unable or unwilling to comply with behavioral restrictions, including refraining from electronic devices displaying time cues unless clocks are removed and devices are disconnected from Wi-Fi * Unable or unwilling to comply with consumption restrictions, including abstaining from caffeine, alcohol, and melatonin-rich foods during the study * Extreme chronotype, defined as a habitual midsleep time outside 03:00-05:00 on the MCTQ or classification as an extreme morning or extreme evening type on the MEQ * Daily caffeine consumption exceeding 400 mg (approximately 4-5 cups of coffee) * Current smoker or smoking within the past six months
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Phase shift in circadian rhythm markers | Comparing samples on days 1, 3, 5 | The primary outcome is the timing of dim light melatonin onset, a marker of circadian phase. Saliva samples will be collected at regular intervals under dim light, and the time when melatonin exceeds 3 pg/mL will be recorded for each participant. This allows measurement of circadian phase shifts across conditions. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Psychomotor Vigilance Task (PVT) Median Reaction Time | Performance will be measured at regular intervals on days 1 - 5 to track changes over the course of the study. | Median reaction time (milliseconds) on a brief psychomotor vigilance task (PVT) six times each day. Participants respond as quickly as possible to visual stimuli presented at random inter-stimulus intervals. For each block, the median reaction time is computed; additional indices such as lapses (responses \> 500 ms) may be derived. Changes in PVT performance across the the 5 days are analysed in relation to circadian phase. |
Countries
Denmark