All registrars in KEMH NICU were invited to participate in the study by email advertising and in-service information sessions. All participants gave written informed consent. Consenting registrars were provided envelopes containing a unique participant identity number and questionnaires. The contents of the envelope included the demographic questionnaire, consensus sleep diary (CSD)-core, self-reported sleepiness questionnaire, and additional data form for each shift (as described below). The participant identity number was used to complete the questionnaires and to perform the PVT to protect confidentiality. Based on their request, the personal details of participating registrars were not collected to protect their confidentiality. There were no exclusion criteria.

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