Inclusion and Exclusion Criteria: Participants were eligible for inclusion if they were at least 18 years old, employed either full-time or part-time, had no history of intercontinental travel in the preceding two weeks, and had not been diagnosed with a sleep disorder.
Recruitment Strategies: Participants were recruited through multiple strategies to ensure a diverse and representative sample. Study announcements were disseminated via university newsletters, reaching postgraduate students and staff directly. Additionally, word of mouth played a role, as participants were encouraged to share information about the study within their networks. Posters were displayed in high-traffic areas such as university buildings, libraries, and communal spaces to attract potential participants.
Initial contact: The initial recruitment contact was established via email following the participant's expression of interest. In response, available time slots, the participant information sheet, and photos of the wearable device were provided for review. If the participant agreed on a specific date and time, they were offered the option to meet at our recruitment office. However, to accommodate individual preferences, meetings could also take place at a mutually agreed-upon public location of their choice.
Before the registration meeting
One day before the registration meeting: A reminder email was sent to participants, including the mobile app download link and instructions for installation. The wearable device was thoroughly sterilized to ensure hygiene and prepared for use. Additionally, the device’s local memory storage was checked and cleared to ensure sufficient capacity for data collection. The device was then left to charge overnight to ensure full battery capacity at the time of distribution. Finally, a functionality test was performed, and any necessary adjustments or fixes were made to ensure optimal performance before the meeting.
Prior to the registration meeting: An anonymized participant ID was generated, a designated folder for storing the participant's results was created, and the blank consent form and study instruction was printed.