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Clinical Trials/NCT02744235
NCT02744235WithdrawnNot Applicable

Sensitivity and Specificity of Mainstream Sleep Tracking Devices Compared to Polysomnography

NYU Langone Health1 site in 1 countryStarted: March 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Locations
1
Primary Endpoint
Number of Minutes of Sleep

Study Overview

Brief Summary

The purpose of this study is to compare two popular portable sleep monitoring devices-the Fitbit Charge®, Jawbone UP®, and SleepTime smartphone app-to the "gold standard" Polysomnography (PSG). Parameters that will be analyzed include sleep onset latency, sleep efficiency, and sleep staging. Specifically, this study will investigate the validity of the Jawbone UP®, Fitbit Charge®, and SleepTime app in detecting sleep and wakefulness in comparison to conventional Polysomnography (PSG).

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Patients undergoing Polysomnography

Exclusion Criteria

  • •severe sleep apnea
  • •severe insomnia with less than two hours of sleep per night
  • •epileptiform activity
  • •electrical status epilepticus of sleep

Arms & Interventions

Patients undergoing Polysomnography

Other

Intervention: Fitbit Charge ® (Device)

Patients undergoing Polysomnography

Other

Intervention: Polysomnography Data (Device)

Patients undergoing Polysomnography

Other

Intervention: Jawbone UP® (Device)

Outcomes

Primary Outcomes

Number of Minutes of Sleep

Time Frame: Up to 3 Months

Time it takes subject to fall asleep

Time Frame: Up to 3 Months

Number of Arousals

Time Frame: Up to 3 Months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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