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Clinical Trials/NCT03489460
NCT03489460CompletedNot Applicable

Research Exploring Sleep Education & Technology

NYU Langone Health1 site in 1 country1,060 target enrollmentStarted: February 1, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
1,060
Locations
1
Primary Endpoint
Sleep time measured by wearable mobile sleep tracking technology

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • A current user of the OURA ring activity and sleep tracker device.
  • For Aim 3 MOST message testing, the inclusion criteria include the following:
  • Health conscious.

Exclusion Criteria

  • Non English speakers.

Outcomes

Primary Outcomes

Sleep time measured by wearable mobile sleep tracking technology

Time Frame: 15 Days

Mobile sleep tracking device will be worn by patient for 15 days and will measure sleep patterns in patients

Time in deep sleep measured by wearable mobile sleep tracking technology

Time Frame: 15 Days

Mobile sleep tracking device will be worn by patient for 15 days and will measure sleep patterns in patients

Dysfunctional Beliefs about Sleep (DBAS) scale

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

Measure of motivation to change using the Change Assessment Scale (CAS)

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"

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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