CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 200 enrolled
Drug / intervention
Fitbit +2 moredevice
Likely dose
Not stated in record
Key inclusion· 1
  • ✓Attending a regularly scheduled overnight polysomnography (PSG) sleep study at Weill Cornell Medical College Center for Sleep Medicine
Key exclusion· 3
  • ✕Age under 18 or over 80 years
  • ✕Pregnancy
  • ✕Unable to provide informed consent

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02779543
NCT02779543N/ACompleted
CompareCT.gov

Clinical Validation of New Commercial Sleep Monitoring Devices

Weill Medical College of Cornell University·interventional·Posted May 20, 2016·Updated Mar 14, 2019

In Brief

A clinical study evaluating Fitbit, Jawbone UP, and 1 other intervention for Sleep Apnea. Completed, enrolled 200 participants across 1 site.

Detailed Summary

This study seeks to validate three new commercial sleep monitoring devices: Fitbit, Jawbone UP, and Microsoft Band by comparison against concurrent polysomnography (PSG), which is considered the gold standard for sleep assessment. This research is being done because if proven to accurately analyze sleep,these devices may make conducting in-home sleep studies easier and more affordable in the future.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSleep Apnea
CountriesUnited States
CollaboratorsCornell University

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedMay 20, 2016
Enrollment StartJun 1, 2018
Primary CompletionJul 30, 2018
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 10.1 years ago

Interventions

Fitbitdevice

Subjects will be recruited from those patients attending a regularly scheduled overnight PSG sleep study at the Weill Cornell Medical College Center for Sleep Medicine. Willing subjects, after providing informed consent, will be fitted with one of the three aforementioned sleep monitoring devices (randomly assigned) on the wrist of their non-dominant hand when prepared for the sleep study by a technician.

Jawbone UPdevice

Subjects will be recruited from those patients attending a regularly scheduled overnight PSG sleep study at the Weill Cornell Medical College Center for Sleep Medicine. Willing subjects, after providing informed consent, will be fitted with one of the three aforementioned sleep monitoring devices (randomly assigned) on the wrist of their non-dominant hand when prepared for the sleep study by a technician.

Microsoft Banddevice

Subjects will be recruited from those patients attending a regularly scheduled overnight PSG sleep study at the Weill Cornell Medical College Center for Sleep Medicine. Willing subjects, after providing informed consent, will be fitted with one of the three aforementioned sleep monitoring devices (randomly assigned) on the wrist of their non-dominant hand when prepared for the sleep study by a technician.