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Mainstream Sleep Tracking Devices vs Polysomnography

NYU Langone Health logo

NYU Langone Health

Status

Withdrawn

Conditions

Epileptiform Activity
Severe Sleep Apnea
Severe Insomnia

Treatments

Device: Jawbone UP®
Device: Polysomnography Data
Device: Fitbit Charge ®

Study type

Interventional

Funder types

Other

Identifiers

NCT02744235
15-00071

Details and patient eligibility

About

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).

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Patients undergoing Polysomnography
Other group
Treatment:
Device: Polysomnography Data
Device: Fitbit Charge ®
Device: Jawbone UP®

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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