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This is a prospective, unblinded, open-label, single group study. All subjects will undergo concurrent screener app, HSAT testing, and in-lab polysomnography.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Concurrent PSG, HSAT, and Screener App Test | Experimental | Participants will undergo a single night baseline PSG test with concurrent HSAT tests as well as non-contact screening mobile apps through a smartphone. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PSG | Diagnostic Test | In-lab sleep polysomnography test |
| |
| Measure | Description | Time Frame |
|---|---|---|
| AHI value. Clinical decision for treatment output (Y to CPAP or N to CPAP) of Screener apps and HSAT compared to PSG. | The PSG clinical decision for treatment is defined as AHI≥15. Screener apps and HSATs provide AHI values that will be used for comparison. | Day 1 |
| Measure | Description | Time Frame |
|---|---|---|
| OSA severity categories (normal, mild, moderate, severe) of Screnner apps and HSAT compared to PSG. | Day 1 |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Clayton Sleep Institute | Maplewood | Missouri | 63143 | United States |
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| ID | Term |
|---|---|
| D020181 | Sleep Apnea, Obstructive |
| D012891 | Sleep Apnea Syndromes |
| ID | Term |
|---|---|
| D001049 | Apnea |
| D012120 | Respiration Disorders |
| D012140 | Respiratory Tract Diseases |
| D020919 | Sleep Disorders, Intrinsic |
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| Home Sleep Apnea Test with FDA cleared devices |
| Diagnostic Test |
In-lab HST test |
|
| Non-Contact Screening App | Other | Non-Contact Sleep Apnea Screening Applications at bedside table to assess for sleep apnea. |
|
| D020920 |
| Dyssomnias |
| D012893 | Sleep Wake Disorders |
| D009422 | Nervous System Diseases |