Evidence map›Paper›PMID 42169202›Full record

ArticleBioelectronic medicine2026

A novel, wearable, in-ear EEG technology to assess sleep and daytime sleepiness.

Jonathan Berent, Prabhjyot Saini, Andrew X Stewart, Devansh Bheda, Konstantin Borodin, Akshay Paul, Brian Tracey, Caroline Dong, Dmitri Volfson, Derek L Buhl and 1 more

Abstract read
In one paragraph

Article in Bioelectronic medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Jonathan BerentNextSense Inc., Mountain View, California, USA. jb@nextsense.io.
Prabhjyot SainiEmory University Dept. of Neurology, Emory Sleep Center, Emory University School of Medicine, Atlanta, Georgia, USA.
Andrew X StewartNextSense Inc., Mountain View, California, USA.
Devansh BhedaInfocusp, Inc., Ahmedabad, India.
Konstantin BorodinNextSense Inc., Mountain View, California, USA.
Akshay PaulNextSense Inc., Mountain View, California, USA.
Brian TraceyTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
Caroline DongEmory University Dept. of Neurology, Emory Sleep Center, Emory University School of Medicine, Atlanta, Georgia, USA.
Dmitri VolfsonTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
Derek L BuhlTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
David B RyeEmory University Dept. of Neurology, Emory Sleep Center, Emory University School of Medicine, Atlanta, Georgia, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In-ear electroencephalography (EEG) has emerged as a promising alternative to traditional in-laboratory sleep studies, offering greater comfort and practicality. Here we present a novel in-ear EEG system, comparing in-ear recordings against scalp EEG channels acquired concurrently as part of polysomnography (PSG). The study enrolled 16 healthy control participants in a single-visit overnight-plus-daytime design, and 8 participants with central disorders of hypersomnolence (CDH) in a randomized crossover daytime design (medication vs. medication-holiday). For overnight sleep recordings, ear-EEG and scalp EEG sleep staging showed substantial agreement (Cohen's [Formula: see text]). For daytime MWT trials, agreement was moderate (Cohen's [Formula: see text]), reflecting the predominance of wake epochs in this paradigm. For the primary Maintenance of Wakefulness Test (MWT) endpoint of sleep onset latency (SOL), at the per-subject level ([Formula: see text])-averaging across trials as in standard clinical practice-agreement was good (ICC = 0.71, [Formula: see text], MAD = 5.1 min). Among the 37 of 126 trials where both devices detected sleep (approximately 30% of trials), agreement was strong (ICC = 0.82, MAD = 1.9 min), with excellent agreement in healthy controls (ICC = 0.95, MAD = 1.2 min). Overall trial-level agreement across all 126 trials was moderate (ICC = 0.55), reflecting 22 discordant trials in which scalp EEG detected sleep but in-ear EEG did not-predominantly brief, subtle N1 transitions, concentrated in a subset of CDH participants. For overnight sleep architecture ([Formula: see text] healthy controls), total sleep time ([Formula: see text], ICC = 0.85), sleep efficiency ([Formula: see text]), and wake after sleep onset ([Formula: see text]) showed strong agreement, with small systematic biases consistent with reduced N1 detection sensitivity. These findings support the feasibility of in-ear EEG for sleep staging and daytime sleepiness assessment in laboratory settings, and motivate larger confirmatory studies-including home-based longitudinal monitoring-to establish clinical utility, particularly in populations with altered sleep architecture.

Indexed as

Central disorders of hypersomnolenceExcessive daytime sleepiness (EDS)Idiopathic hypersomnia (IH)In-ear EEGMaintenance of wakefulness test (MWT)Narcolepsy (NT1, NT2)PSGSleep wearables

Identifiers

PMID42169202
PMCPMC13195905

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.