Clinical Validation of New Commercial Sleep Monitoring Devices

NACompletedINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

June 1, 2018

Primary Completion Date

July 30, 2018

Study Completion Date

July 30, 2018

Conditions
Sleep Apnea
Interventions
DEVICE

Fitbit

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.

DEVICE

Jawbone UP

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.

DEVICE

Microsoft Band

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.

Trial Locations (1)

10065

Weill Cornell Medicine Center for Sleep Medicine, New York

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Cornell University

OTHER

lead

Weill Medical College of Cornell University

OTHER

NCT02779543 - Clinical Validation of New Commercial Sleep Monitoring Devices | Biotech Hunter | Biotech Hunter