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Comparison Between Multiple Wrist-worn Actigraphy Devices and Polysomnography

NCT02463461 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2017-05-10

No results posted yet for this study

Summary

The primary objective of the proposed study is to investigate the agreement levels of modern and well-established actigraphy devices against PSG in healthy as well as patient populations for multiple sleep parameters across two study sites (Qatar and New York City).

Conditions

Interventions

DEVICE

ActiSleep Activity Monitor

Subjects in this group will wear a ActiSleep Activity Monitor.

DEVICE

Jawbone Activity Monitor

Subjects in this group will wear a Jawbone Activity Monitor.

DEVICE

Actiwatch 2 Activity Monitor

Subjects in this group will wear a Actiwatch 2 Activity Monitor.

DEVICE

FitBit Activity Monitor

Subjects in this group will wear a FitBit Activity Monitor.

DEVICE

Actigraph by Ambulatory Monitoring Activity Monitor

Subjects in this group will wear a Actigraph by Ambulatory Monitoring Activity Monitor.

Sponsors & Collaborators

  • Weill Cornell Medical College in Qatar

    collaborator OTHER

  • Weill Medical College of Cornell University

    lead OTHER

Principal Investigators

  • Ana Krieger · Weill Medical College of Cornell University

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2017-07-31
Completion
2017-08-31

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Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02463461 on ClinicalTrials.gov