#SMARTSLEEP RESEARCH ARTICLES FULL#
#SMARTSLEEP RESEARCH ARTICLES TRIAL#

#SMARTSLEEP RESEARCH ARTICLES FULL#

After a full explanation of the protocol and after all the participants' questions have been answered, they will be asked to sign the consent form. A detailed interview will be performed verifying eligibility criteria, as well as a review of work and non-work schedules. Participants will be asked to report to the research site for a daytime visit. Visit 1 (Screening) Procedures (up to 2 hours): Healthy Sleep Deprivation Insufficient Sleep Syndromeĭevice: SmartSleep Boost On Device: SmartSleep Boost Off The anticipated study duration will be up to 6 weeks (including the 4 weeks of use period). The final visit will be an in facility visit in which all study equipment will be returned. Additional phone calls may occur on an as needed basis if issues arise. Participants will be asked to complete a question twice daily during the home use period. Participants will be asked to complete a battery of cognitive tests upon wake up each morning. Study staff will contact participants after the first week of use as a reminder. The home use will include an initial week of baseline use followed by 3 weeks of use with boost on. The study involves an initial screening visit followed by home use of the SmartSleep device with SleepMapper app. Up to 75 individuals will be consented in order to complete a total of 50 participants using a nonrandomized design. In addition, participants diagnosed with major organ system diseases or requiring oxygen therapy are excluded from participation. Participants are generally healthy individuals who have not been diagnosed with any sleep-related medical conditions. In addition, participants report a sleep latency ≤ 30 minutes less than or equal to 3 nights per week. Participants also increase their sleep duration by ≥ 1 hour on the weekends. of sleep per night, and sleeping less than or equal to 7 hrs. For the purposes of this study, shortened sleep is defined as sleeping at least 5 hrs. old) who are working full time and report shortened sleep due to lifestyle. It is intended to provide data related to product use and cognitive testing incorporating a longer baseline period for comparison purposes.

#SMARTSLEEP RESEARCH ARTICLES TRIAL#

This study is a nonrandomized, unblinded, uncontrolled case series clinical trial validating the SmartSleep product, including SleepMapper app in the home setting.

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Smartsleep research articles