Those that have been nicotine-free for 30 days will be included. Current smoker/tobacco user, or using nicotine replacement therapy.Excessive caffeine consumption (> 650mg/day combining all caffeinated drinks regularly absorbed during the day).Free of psychological/psychiatric conditions that preclude participation.Bachelor's degree or Master's degree (or the equivalent in work experience) in a relevant field, and/or military service.In addition, both study personnel and those assessing outcomes will not be aware of the order of stimulation modalities.Įvaluation of SmartSleep Technology for Improving the Efficiency and Restorative Quality of Sleep in Healthy Adults in Order to Mitigate Cognitive Performance Deficits Due to Sleep Restriction and Emergency Awakenings Subjects will wear the SmartSleep device each night and will be unaware of the order of stimulation modalities. The SmartSleep device will be programmed by investigators not involved in study execution. Triple (Participant, Investigator, Outcomes Assessor) Each subject will receive all of the 4 sleep conditions in a randomized order that will be unknown to the subject. This study uses within subject randomization. Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information Subjects will complete the 7-day study in groups of 4. A total of 12 healthy astronaut-like adults will be studied.
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