0687 Validation of Waveband for Capturing Sleep in Hypersomnia Disorders

Abstract Introduction Narcolepsy type 1 (NT1) is a rare neurological disorder linked to orexin deficiency. It is characterized by excessive daytime sleepiness, cataplexy, hallucinations, sleep paralysis, disrupted nighttime sleep, and cognitive symptoms. Diagnosis and therapeutic evaluation rely on in-clinic polysomnography (PSG) and multiple sleep latency testing (MSLT), which can be resource-intensive, burdensome, and inconsistent. NCT06531876 evaluated Waveband, an FDA-cleared at-home dry-electrode electroencephalogram (EEG), in individuals with NT1 and suspected central disorders of hypersomnolence (CDH). Following data collection, a new Waveband sleep-staging algorithm (WSSA) was implemented under an FDA-authorized Predetermined Change Control Plan. Methods Seventy-five participants (50 NT1; 25 suspected CDH) undertook six nights of at-home Waveband sleep recording and one 24-hour recording, followed by one or two nights of in-clinic PSG and a single MSLT, each with concurrent Waveband recording. Wear-time compliance and data quality were assessed via existing algorithms. PSG/MSLT data were scored by three registered PSG technologists, and Waveband data were scored using the WSSA. Results All participants completed ≥4 overnight recordings with ≥4 hours of wear time (mean [SD]: 7.9 [1.8] hours/night, 98% [5%] of data deemed scorable). For the 24-hour period, 93% of participants had ≥17 hours of wear time (mean [SD]: 22.2 [2.7] hours, 99% [1%] of data deemed scorable). The updated WSSA demonstrated high agreement with PSG in NT1 participants (mean Cohen’s Kappa: 0.81) and positive agreement across sleep stages: wake (87%), NREM1 (59%), NREM2 (87%), NREM3 (82%), and REM (90%) sleep. It accurately identified sleep-onset REM periods during PSG/MSLT with 74/76% sensitivity and 100/97% specificity. Concordance (ICC) between Waveband and PSG macrofeatures was strong, including sleep efficiency (0.94), wake after sleep onset (0.95), sleep onset latency (0.89 [PSG], 0.90 [MSLT]), and REM within 120 minutes of sleep onset (0.87). Comparable performance was seen in participants with suspected CDH. Conclusion Waveband enables accurate, scalable at-home sleep evaluation in hypersomnia with high compliance and data quality. The updated WSSA outperforms the prior algorithm and reliably detects EEG features of narcolepsy. These results support the use of Waveband in NT1 clinical trials and for real-world clinical evaluations of cases with suspected hypersomnolence disorders. Support (if any) Funded by Takeda and Beacon Biosignals.

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Journal
SLEEP
Published
2026-05-01
DOI
https://doi.org/10.1093/sleep/zsag091.0686
Primary Topic
Sleep and Wakefulness Research
Type
article
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article

0687 Validation of Waveband for Capturing Sleep in Hypersomnia Disorders

Marta Karas, Tarik Yardibi, Katerina Placek, Dennis Hwang et al.
SLEEP
Sleep and Wakefulness Research
article

0687 Validation of Waveband for Capturing Sleep in Hypersomnia Disorders

Marta Karas, Tarik Yardibi, Katerina Placek, Dennis Hwang, Jayne Nerrie, Brian Tracey, Emmanuel Mignot, Patrick Tierney, Alexander Chan, Jason Manley, Antoine Guillot, Jay Pathmanathan, Dmitri Volfson, Jacob Donoghue, Rebecca Reh
article en

Abstract

Abstract Introduction Narcolepsy type 1 (NT1) is a rare neurological disorder linked to orexin deficiency. It is characterized by excessive daytime sleepiness, cataplexy, hallucinations, sleep paralysis, disrupted nighttime sleep, and cognitive symptoms. Diagnosis and therapeutic evaluation rely on in-clinic polysomnography (PSG) and multiple sleep latency testing (MSLT), which can be resource-intensive, burdensome, and inconsistent. NCT06531876 evaluated Waveband, an FDA-cleared at-home dry-electrode electroencephalogram (EEG), in individuals with NT1 and suspected central disorders of hypersomnolence (CDH). Following data collection, a new Waveband sleep-staging algorithm (WSSA) was implemented under an FDA-authorized Predetermined Change Control Plan. Methods Seventy-five participants (50 NT1; 25 suspected CDH) undertook six nights of at-home Waveband sleep recording and one 24-hour recording, followed by one or two nights of in-clinic PSG and a single MSLT, each with concurrent Waveband recording. Wear-time compliance and data quality were assessed via existing algorithms. PSG/MSLT data were scored by three registered PSG technologists, and Waveband data were scored using the WSSA. Results All participants completed ≥4 overnight recordings with ≥4 hours of wear time (mean [SD]: 7.9 [1.8] hours/night, 98% [5%] of data deemed scorable). For the 24-hour period, 93% of participants had ≥17 hours of wear time (mean [SD]: 22.2 [2.7] hours, 99% [1%] of data deemed scorable). The updated WSSA demonstrated high agreement with PSG in NT1 participants (mean Cohen’s Kappa: 0.81) and positive agreement across sleep stages: wake (87%), NREM1 (59%), NREM2 (87%), NREM3 (82%), and REM (90%) sleep. It accurately identified sleep-onset REM periods during PSG/MSLT with 74/76% sensitivity and 100/97% specificity. Concordance (ICC) between Waveband and PSG macrofeatures was strong, including sleep efficiency (0.94), wake after sleep onset (0.95), sleep onset latency (0.89 [PSG], 0.90 [MSLT]), and REM within 120 minutes of sleep onset (0.87). Comparable performance was seen in participants with suspected CDH. Conclusion Waveband enables accurate, scalable at-home sleep evaluation in hypersomnia with high compliance and data quality. The updated WSSA outperforms the prior algorithm and reliably detects EEG features of narcolepsy. These results support the use of Waveband in NT1 clinical trials and for real-world clinical evaluations of cases with suspected hypersomnolence disorders. Support (if any) Funded by Takeda and Beacon Biosignals.

SLEEPVol. 49(Supplement_1)
Kaiser Permanente (US), Beacon College (US), Stanford Medicine (US), Takeda (United States) (US), Stanford University (US)
Openalex Percentile: Top 7%
Sleep and Wakefulness Research
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