None listed
Conditions
Brief summary
This study aims to investigate the optimal duration of on-shift naps during night shifts to improve safety and productivity. While on-shift naps can boost performance at night, they may temporarily reduce alertness upon waking and require additional downtime away from work tasks. In a controlled laboratory setting, participants will complete four conditions in a within-subjects, repeated measures, counterbalanced design: no-nap; 15-min nap; 30-min nap; 60-min nap. We hypothesise that increasing the duration of naps will result in an overall increase in whole of shift performance and productivity, despite greater short-term safety impairment from sleep inertia post-nap. The findings will support evidence-based guidelines for on-shift napping to support workplace productivity and safety with minimal disruption to operational efficiency.
Interventions
Arm 1: 15 minute nap condition Intervention: Participants are assigned to a 15 min nap opportunity during a scheduled break, within a 12-hour simulated night shift protocol. Who delivers it and their relevant expertise: The research is delivered by a research team with extensive expertise in sleep and fatigue research. There will be one postdoctoral research fellow, two PhD candidates and trained research assistants conducting the data collection. How is it delivered: The study is conducted in a controlled sleep laboratory. Participants are assigned to individual bedrooms within a six-bedroom sleep laboratory facility. How often and for how long: Each experimental condition lasts 40 hours and includes one adaptation night and the following night is a 12-hour simulated night shift where cognitive test batteries and simulated work tasks will be completed throughout the shift. Participants reside in the laboratory for the duration of each condition. The study uses a randomised counterbalanced design with a 5–7-day washout period between conditions. Where is it delivered: A state of the art six-bedroom sleep laboratory facility. Adherence: Participants are continuously monitored during laboratory stays. Between experimental conditions, adherence is supported through sleep diaries, food diaries and actigraphy monitoring. Arm 2: 30-minute nap condition Intervention: Intervention: Participants are assigned to a 30 min nap opportunity during a scheduled break, within a 12-hour simulated night shift protocol. (All other components are identical to Arm 1) Arm 3: 60-minute nap condition Intervention: Intervention: Participants are assigned to a 60 min nap opportunity during a scheduled break, within a 12-hour simulated night shift protocol. (All other components are identical to Arm 1)
Sponsors
Study design
Eligibility
Inclusion criteria
- Healthy participants aged 18-40 years. - Male or female - Body Mass Index (BMI) between 18.00-29.99 kg/m2 - Intermediate chronotype (determined by the Morningness/Eveningness questionnaire score) - No diagnosed sleep disorders - Not taking medication known to impact sleep
Exclusion criteria
- Smoker - Use of recreational drugs - Currently taking prescription drugs that impact sleep - Pittsburgh Sleep Quality Index score > 5. - Epworth Sleepiness Scale score > 10 - Insomnia Severity Index score > 15 - Trans meridian travel (> 2 time zones) or shiftwork in the last 3 months. - > 2 alcohol beverages per day - Daily caffeine consumption > 400 mg - > 2 positive responses on Berlin Sleep Questionnaire - Extreme chronotype (determined by the Morningness/Eveningness questionnaire score)