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OpenTrials
Completed

NCT Number: NCT02967367

Reliability of Consumer Sleep Trackers in Patients Suffering From Obstructive Sleep Apnea Syndrome

During last years, numerous sleep trackers have been commercialized. They are intended to give indications about sleep quality/duration in order to give people an internet-based feedback about their own sleep.

For clinical and research purposes, tri-axial accelerometers/multi-sensors devices are used routinely to assess objective sleep quality/patterns. Their use is also validated to estimate sleep in obstructive sleep apnea syndrome (OSA).

The purpose of the present study is to compare the accuracy of consumer-level sleep trackers and validated tools to measure sleep in OSA patients.

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Key information

Conditions

Obstructive Sleep Apnea Syndrome Apnea Dyssomnias Nervous System Diseases Respiration Disorders Respiratory Tract Diseases Sleep Apnea Syndromes Sleep Apnea, Obstructive Sleep Disorders, Intrinsic Sleep Wake Disorders

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHu Saint Pierre

Brussels, 1000, Belgium

About this study

During last years, numerous sleep trackers have been commercialized. They are working on accelerometer-based technology. They are intended to give indications about sleep quality/duration in order to give people an internet-based feedback about their own sleep..

For clinical and research purposes, tri-axial accelerometers/multi-sensors devices are used routinely to assess objective sleep quality/patterns. Their use is also validated to estimate sleep in obstructive sleep apnea syndrome (OSA).

The purpose of our study is to compare the accuracy of consumer-level sleep trackers and validated tools to measure sleep in OSA patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • high clinical suspicion of obstructive sleep apnea syndrome

Exclusion criteria

  • other associated sleep disorder
  • inability to sign informed consent

Treatment and study plan

Jawbone sleep tracker

Device

During one night of polysomnographic recording, investigators are going to place these 3 accelerometers on the wrist of the patient

Other names: accelerometer

Withings sleep tracker

Device

During one night of polysomnographic recording, investigators are going to place these 3 accelerometers on the wrist of the patient

BodyMedia Sense Wear accelerometer

Device

During one night of polysomnographic recording, investigators are going to place these 3 accelerometers on the wrist of the patient

Primary outcomes

  1. Time in Bed

    Time frame: one night (up to 600 minutes)

    time spent in bed during the night (minutes)

  2. Sleep Efficiency

    Time frame: one night (up to 600 minutes)

    a percentage corresponding to total sleep time divided by time in bed

  3. Total Sleep Time

    Time frame: one night (up to 600 minutes)

    time spent sleeping during the night (minutes)

Secondary outcomes

  1. Deep Sleep

    Time frame: one night (up to 600 minutes)

    a percentage corresponding to sleep time spent in deep sleep (stage N3 on polysomnography) divided by total sleep time

  2. Light Sleep

    Time frame: one night (up to 600 minutes)

    a percentage corresponding to sleep time spent in light sleep (stage N1 and N2 on polysomnography) divided by total sleep time

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire Saint Pierre

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Nov 18, 2016
Registry last updated
Mar 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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