Reliability of the Samsung Galaxy for the Detection of Moderate to Severe Obstructive Sleep Apnea

Last updated: March 7, 2025
Sponsor: Stanford University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Sleep Apnea Syndromes

Treatment

Samsung Galaxy Watch

Clinical Study ID

NCT06603441
76129
  • Ages > 22
  • All Genders

Study Summary

The study will test the reliability of the Samsung Galaxy for the Detection of Moderate to Severe Obstructive Sleep Apnea (OSA)

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 22 years of age or older

  • High pre-test likelihood of moderate to severe obstructive sleep apnea (OSA) basedon screening questionnaires (STOP-Bang and Epworth Sleepiness Scale); or priordiagnosis of moderate-severe OSA.

  • Able to provide informed consent confirmation

Exclusion

Exclusion Criteria:

  • Severe and/or other acute medical illnesses as determined by the Investigator, inparticular: Cardiac conditions such as Congestive Heart Failure (CHF), atrialfibrillation, Hx of Movement disorders: Parkinson's, Tremor, Lung conditions:Chronic Obstructive Pulmonary Disease (COPD), chronic bronchitis, emphysema,pulmonary fibrosis, acute episode of flu, allergies, asthma.

  • Active comorbid sleep disorders, such as severe insomnia, restless legs syndrome,Periodic Leg Movement During Sleep (PLMS), narcolepsy, idiopathic hypersomnia

  • Severe and/or unstable psychiatric disorders such as mood, anxiety, or psychoticdisorders

  • Individual has a condition the Investigator believes would interfere with his or herability to provide informed consent, comply with the study protocol, which mightconfound the interpretation of the study results or put the person at undue risk

  • Inability to use a Samsung Galaxy device for sleep tracking

  • Inability to have two nights in the Stanford sleep lab.

  • Participants who are pregnant

  • Tattoos or scars covering the forearm area of both hands

Study Design

Total Participants: 150
Treatment Group(s): 1
Primary Treatment: Samsung Galaxy Watch
Phase:
Study Start date:
December 17, 2024
Estimated Completion Date:
February 28, 2026

Study Description

A prospective cohort of 150 individuals 22 years or older with a prior diagnosis or with a high likelihood of having moderate to severe OSA, screened using STOP-Bang and Epworth Sleepiness Scale questionnaires will be recruited and will utilize the Samsung Galaxy Watch technology to monitor sleep patterns, oxygen saturation, PPG, and heart rate variability amongst other physiologic parameters. All data will be collected over the course of two intervention nights in the sleep lab and at home for three nights.

Connect with a study center

  • Stanford University

    Palo Alto, California 94305
    United States

    Active - Recruiting

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