Evidence map›Paper›PMID 42456159›Full record

ArticleJMIR mHealth and uHealth2026

Passive Screening for Depressive Symptoms Using Daily Wrist Actigraphy and Deep Learning: Model Development and Validation Study.

Doljinsuren Enkhbayar, Somin Oh, Jinhee Lee, Min-Hyuk Kim, Erdenebayar Urtnasan, Jaehong Key

Abstract read
In one paragraph

Article in JMIR mHealth and uHealth, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Doljinsuren EnkhbayarDepartment of Biomedical Engineering, Mirae campus, Yonsei University, 1, Yeonsedae-gil, Heungeop-myeon, Wonju-si, Gangwan-do, 26493, Republic of Korea, 82 33 760 5270, 82 33 760 2919.ORCID 0009-0002-7858-3966
Somin OhDepartment of Biomedical Engineering, Mirae campus, Yonsei University, 1, Yeonsedae-gil, Heungeop-myeon, Wonju-si, Gangwan-do, 26493, Republic of Korea, 82 33 760 5270, 82 33 760 2919.ORCID 0009-0006-3059-9108
Jinhee LeeDepartment of Psychiatry, Wonju College of Medicine, Yonsei University Mirae Campus, Wonju, Gangwon-do, Republic of Korea.ORCID 0000-0003-4255-1831
Min-Hyuk KimDepartment of Psychiatry, Wonju College of Medicine, Yonsei University Mirae Campus, Wonju, Gangwon-do, Republic of Korea.ORCID 0000-0002-6130-3254
Erdenebayar Urtnasan *Division of AI Semiconductor, Yonsei University Mirae Campus, Wonju, Gangwon-do, Republic of Korea.ORCID 0000-0002-3493-9724
Jaehong Key *Department of Biomedical Engineering, Mirae campus, Yonsei University, 1, Yeonsedae-gil, Heungeop-myeon, Wonju-si, Gangwan-do, 26493, Republic of Korea, 82 33 760 5270, 82 33 760 2919.ORCID 0000-0002-3453-2123

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Depressive symptoms are common yet often underrecognized in routine care, underscoring the need for scalable screening approaches beyond episodic self-report assessments. Wearable actigraphy can passively and continuously capture daily activity and 24-hour rest-activity rhythms associated with depressive symptom burden. However, the performance of artificial intelligence (AI) models that leverage actigraphy data for depressive symptom screening remains insufficiently established. Objective: This study aimed to develop and evaluate AI-based models for passive screening of depressive symptoms from daily wrist actigraphy data. Methods: We analyzed actigraphy recordings from 1160 Hispanic/Latino adults in the Hispanic Community Health Study/Study of Latinos who completed the 10-item Center for Epidemiologic Studies Depression scale (CESD-10), a self-reported depressive symptom screening scale. Multichannel actigraphy data, including activity counts, light exposure, and wake status, were used as inputs to 5 deep learning architectures to classify CESD-10-defined depressive symptom groups, comparing mild and higher symptoms with the normal group. Results: Actigraphy-derived behavioral markers differed across depressive symptom groups, showing lower daytime activity and altered circadian rest-activity organization with increasing symptom burden. Among the 5 deep learning architectures evaluated, the long short-term memory model consistently demonstrated the strongest overall discrimination. In held-out testing, the long short-term memory model achieved a macro-averaged area under the receiver operating characteristic curve of 0.80, with the strongest discrimination observed for the higher depressive symptom group (area under the receiver operating characteristic curve 0.889). These findings indicate improved model discrimination with increasing symptom severity, although false-positive rates remained notable across both classification tasks. Conclusions: Our study suggests that actigraphy-derived data can support AI-based classification of depressive symptoms. An actigraphy-based AI model may serve as a scalable, passive, and noninvasive complementary signal to aid early screening alongside traditional depressive symptom assessments before clinical diagnosis.

Indexed as

ActigraphyDeep LearningDepressionMass ScreeningAdultFemaleHumansMaleMiddle AgedROC CurveWristactigraphyartificial intelligencedeep learningdepression screeningdepressive symptomspassive monitoringwearable devices

Identifiers

PMID42456159
PMCPMC13372263

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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.