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Snoring Sound Analysis for the Diagnosis of Patients with suspected Obstructive Sleep Apnoea

Comparison of a snoring sound analysis algorithm against polysomnography for the diagnosis of obstructive sleep apnoea in patients attending a Sleep Disorders Centre: a diagnostic test accuracy study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000409471
Enrollment
31
Registered
2016-03-30
Start date
2018-04-04
Completion date
2021-03-02
Last updated
2020-02-10

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

Conditions

None listed

Brief summary

It has been well established in the literature that snoring sounds can be used to detect the presence of obstructive sleep apnoea (OSA). Currently the gold standard in the diagnosis of obstructive sleep apnoea is Type I Polysomnography (PSG), which is both time and resource intensive. Streamlining the diagnostic process for patients with OSA is of great significance given the increasing prevalence and awareness of the condition. Retrospective pilot studies have been conducted previously through our unit to assess the utility of analysing snoring sounds as a predictor for obstructive sleep apnoea. Our proposed study aims to systematically explore the performance of our snore/breathing sound technology algorithm against Type I PSG by conducting a statistically powered study in a sleep laboratory as well as a home setting. We hypothesise that breathing sounds (including snoring), when analysed using appropriate mathematical methods and machine learning techniques, can provide sufficient information to detect OSA at a sensitivity and specificity >92% simultaneously, with respect to Type 1 PSG. It is planned to prospectively recruit up to 50 patients with suspected sleep disordered breathing who are already listed for diagnostic PSG study in our sleep lab. These patients will undergo the sleep study as planned, and will undergo a slightly modified protocol with additional sound measurements, along with oesophageal pressure monitoring. The patient will then proceed to have another 7 nights data collected with a portable sound recorded (stored as an "app" on a provided smart phone) to further validate data against PSG. Analysis of the recorded snoring sounds using the externally developed algorithim will then be correlated against Apnoea-Hypopnoea Index (AHI) as measured during the PSG, which is considered the current diagnostic gold standard. Ideally this information will aid in the validation of a streamlined technique to be used in the diagnosis of sleep disordered breathing.

Interventions

Our proposed study aims to systematically explore the performance of our snore/breathing sound technology algorithm against Type I Polysomnography (PSG) by conducting a statistically powered study in a sleep laboratory as well as a home setting. We hypothesise that breathing sounds (including snoring), when analysed using appropriate mathematical methods and machine learning techniques, can provide sufficient information to detect Obstructive Sleep Apnoea (OSA) at a sensitivity and specificity

Our proposed study aims to systematically explore the performance of our snore/breathing sound technology algorithm against Type I Polysomnography (PSG) by conducting a statistically powered study in a sleep laboratory as well as a home setting. We hypothesise that breathing sounds (including snoring), when analysed using appropriate mathematical methods and machine learning techniques, can provide sufficient information to detect Obstructive Sleep Apnoea (OSA) at a sensitivity and specificity >92% simultaneously, with respect to Type 1 PSG. It is planned to prospectively recruit up to 50 patients with suspected sleep disordered breathing who are already listed for diagnostic PSG study in our sleep lab. These patients will undergo a one night diagnostic PSG sleep study as per usual practice in the sleep laboratory. In addition, study subjects will have sound measurements recorded (with a portable sound recorder, installed on a smart phone), along with oesophageal pressure monitoring. Following the first night in the laboratory the next phase of snoring sound data collection will occur at home over the next 7 nights. Subjects will be loaned a smart phone for 7 nights, with an application ("app") installed to achieve this. The smart phone "app" will be self activated by patients when going to sleep, and switched off when awakening. The app solely records snoring sounds during the night for later analysis by our software. No other data collection will take place during this phase. The timing of the activation of the "app" can be correlated against a sleep diary to confirm appropriate use. Data from the PSG will be analysed in the usual fashion by sleep physicians. Analysis of the recorded snoring sounds using the externally developed algorithm will then be correlated against Apnoea-Hypopnoea Index (AHI) as measured during the PSG by the principal investigators. This information will aid in the validation of a streamlined technique to be used in the diagnosis of sleep disordered breathing.

Sponsors

Department of Respiratory and Sleep Medicine Princess Alexandra Hospital.
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Primary purpose
Diagnosis

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients listed for PSG studies through the Sleep Disorders Centre

Exclusion criteria

1. intellectual impairment or inability to provide valid consent. 2. Less than 18 years old.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026