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Validation of Sleep Apnea Diagnosis Device

Validation of a Wireless Wearable Sensor Using Mobile Technology and Cloud Computing for the Diagnosis of Sleep Apnea

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03526133
Enrollment
300
Registered
2018-05-16
Start date
2017-07-07
Completion date
2019-02-07
Last updated
2019-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Apnea

Keywords

sleep apnea, polygraph, home sleep apnea test (HSAT), apnea hypopnea index (AHI), oxygen desaturation index (ODI), portable monitor, sleep actimetry, snoring

Brief summary

Obstructive sleep apnea (OSA) is common and largely underdiagnosed disease. The standard method for the diagnosis of OSA is a complete night polysomnography (PSG). Simple methods for OSA diagnosis are necessary. The overnight oximetry with the oxygen desaturation index (ODI) has been largely investigated as a diagnostic test for OSA but its accuracy remains undefined. The aim of our study is to evaluate if an wireless polygraph (Oxistar) is accurate to diagnosis OSA in patients referred to a Sleep Lab.

Detailed description

Consecutive patients referred to the sleep laboratory with suspected diagnosis of OSA underwent in-laboratory polysomnography (PSG) and simultaneously wireless polygraph. The PSG oximeter and the wireless polygraph were worn on different fingers of the same hand. All sleep studies were reviewed by one blind investigator according the 2017 American Academy of Sleep Medicine recommendations. The number of desaturations from wireless polygraph at the 3 predefined threshold levels (of ODI-2%, ODI-3%, or ODI-4%) was derived automatically using proprietary algorithm. Moderate to severe OSA was defined as AHI ≥ 15 events/h. The diagnostic accuracy of ODI-2%, 3%, and 4% for the diagnosis of moderate-severe OSA were calculated for cut-off values from 1 to 20 desaturation events/h. The sleep actimetry was compared with the sleep stages from PSG, most of the statistical metrics applied for diagnosis were used to evaluate the applicability of this proposed method. Finally, the snoring events computed by the smartphone application were compared with the events heard by a specialist and the statistical comparison metrics were evaluated.

Interventions

DIAGNOSTIC_TESTPolysomnography (PSG) and wireless sensor Oxistar

Monitoring the apnea-hypopnea index (AHI) derived from PSG and the oxygen desaturation index (ODI) obtained by the Oxistar.

Sponsors

Biologix Sistemas Ltda
CollaboratorUNKNOWN
University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* referred by medical staff for an overnight assessment for suspected sleep apnea

Exclusion criteria

* polysomnography for the CPAP titration

Design outcomes

Primary

MeasureTime frameDescription
SpecificityNight during the polysomnography examSpecificity of Oxistar device to detect apnea events compared to gold-standard polysomnography
Bland-Altman GraphNight during the polysomnography examThe Bland-Altman graph evaluates the agreement between the gold-standard polysomnography and Oxistar device
Interclass Correlation Coefficient (ICC)Night during the polysomnography examICC measures the reliability of measurements or ratings between the gold-standard polysomnography and Oxistar device
SensitivityNight during the polysomnography examSensitivity of Oxistar device to detect apnea events compared to gold-standard polysomnography
Area under the curve (AUC)Night during the polysomnography examAUC from ROC curves reflects the accuracy of Oxistar device to detect apnea events compared to gold-standard polysomnography

Secondary

MeasureTime frameDescription
Number of snoring events per hour of register (snoring/h)Night during the polysomnography examSnoring is one of the signs suggestive of obstructive sleep apnea and has recently been considered as having great diagnostic potential. The smartphone application (app) through microphone performs the recording and the characteristics extraction of the patient's audio during sleep (register time). A multilayer perceptron (MPL) neural network classifies the event as snoring or non-snoring. Lastly, the amount of snoring occured is accounted and divided by the register time leading to the number of snoring/h. The agreement between snoring/h measured by the app and the heard by a specialist will be assessed by calculating sensitivity, specificity, accuracy and area under the curve (AUC).
Sleep ActigraphyNight during the polysomnography examActigraphy is the continuous measurement of activity or movement with the use of a small device called an actigraph. Periods of movement suggest wakefulness while those of relative stillness would likely correspond to sleep or quiescence. The Oxistar has a embeded actigraph whose data will be compared with the sleep stage scoring from polysomnography (PSG), the gold standard for sleep assessment. Epoch-by-epoch (30 seconds) agreement between the actigraph and PSG will be assessed by calculating sensitivity, specificity, accuracy, area under the curve (AUC), Bland-Altman graph and interclass correlation coefficient (ICC)

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026