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Evaluating the Diagnostic Efficacy of Smartwatch and Smartphone for Sleep Apnea

NCT06573372 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 295

Last updated 2024-10-18

No results posted yet for this study

Summary

The purpose of this study is to evaluate the diagnostic value of smartphones and watches for OSA screening. The study will be conducted in individuals suspected of having OSA. Subjects will undergo "gold standard" PSG assessment (overnight polysomnography with staff supervision) in a sleep monitoring room, while wearing a smartwatch and smartphone for monitoring. The results will be compared to evaluate the diagnostic value of smartwatches and smartphones for OSA.

Conditions

  • Sleep Apnea, Obstructive

Sponsors & Collaborators

  • OPPO

    collaborator UNKNOWN

  • Peking University First Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-08-29
Primary Completion
2025-03-26
Completion
2026-07-31

Countries

  • China

Study Locations

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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 NCT06573372 on ClinicalTrials.gov