New York University School of Medicine
New York, 10016, United States
NCT Number: NCT03489460
A pilot study that seeks to develop a set of typologies of users of mobile sleep tracking technologies, and optimal sleep health educational strategies among users of mobile wearable technologies that track sleep.
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Notify Me18 year–99 year
All sexes
Interventional
Not applicable
New York, 10016, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
For Aim 3 MOST message testing, the inclusion criteria include the following:
Exclusion criteria
Over the course of 2 weeks' participants will receive specialized sleep-related message interventions to encourage sleep awareness via the smartphone application.
Survey responses will be merged with objective GAD data (sleep time, time in deep sleep, physical activity) which will assist in developing message design formats for message testing.
Time frame: 15 Days
Mobile sleep tracking device will be worn by patient for 15 days and will measure sleep patterns in patients
Time frame: 15 Days
Mobile sleep tracking device will be worn by patient for 15 days and will measure sleep patterns in patients
Time frame: 1 Day
24-item DBAS scale with five subscales corresponding to: (1) consequences of insomnia (2) control and predictability of sleep (3) sleep requirement expectations (5) sleep-promoting practices
Time frame: 15 Days
8 scale measure divided into 4 separate scales: Scale 1: "Pre-Contemplation" Scale 2: "Contemplation" Scale 3 "Action" Scale 4 "Maintenance"
NYU Langone Health
Other
Acronym: RESET
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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