Accepted for/Published in: JMIR mHealth and uHealth
Date Submitted: Aug 15, 2025
Open Peer Review Period: Sep 3, 2025 - Oct 29, 2025
Date Accepted: Nov 22, 2025
(closed for review but you can still tweet)
Warning: This is an author submission that is not peer-reviewed or edited. Preprints - unless they show as "accepted" - should not be relied on to guide clinical practice or health-related behavior and should not be reported in news media as established information.
Multi-Modal Sleep Measurement and Alignment Analysis in Outpatients with Major Depressive Episode: Observational Study
ABSTRACT
Background:
Sleep is essential for overall health and plays a critical role in the diagnosis of psychiatric disorders. Although polysomnography (PSG) remains the gold standard for measuring sleep, its reliance on laboratory settings limits its feasibility for long-term, naturalistic monitoring, particularly for patients with mental disorders.
Objective:
This study assesses sleep tracking reliability and alignment in healthy individuals and mood disorder patients using wearables, nearables, and Ecological Momentary Assessment (EMA), while examining measurement biases and the impact of seasonal and demographic factors on discrepancies across methods.
Methods:
A 14-day study conducted in Finland enrolled a total 201 participants, comprising of patients with a major depressive episode and healthy controls. 172 participants with sufficient observations were retained for further analyses. Participants’ sleep patterns (onset, offset, and total sleep time (TST)) were gathered daily from an actigraph (Actiwatch 2), a bed sensor (Murata SCA11H), mobile screen events, and a daily survey. The alignment between sleep measurement methods was evaluated using Bland-Altman plots and Pearson correlation. Linear mixed models were used to assess the effects of demographics, season, and disorder type on the sleep measures alignment.
Results:
Patients exhibited greater variability in sleep measures than healthy controls. For sleep onset, mean biases between devices were small and not statistically significant in either group, with moderate to strong correlations. In contrast, sleep offset showed significantly larger biases in patients: actigraph vs bed (+34.9 min, P=.013), phone vs bed (–45.3 min, P=.0037), and actigraph vs phone (+78.7 min, P<.001), while controls exhibited minimal and non-significant differences. For TST, phone underestimates sleep compared to both bed sensors (-0.71 min, P<.001) and actigraphs (-1.35 min, P<.001). Across devices, TST correlations remained low, spanning r = 0.12 (p = .58) to r = 0.55 (p = .10) in controls and r = 0.17 (p = .19) to r = 0.43 (p = .002) in patients. Mixed models showed that older age was linked to better sleep offset alignment between actigraphy and bed sensors (β=−0.02, 95% CI −0.04 to 0.00, P=.048), as well as smartphone and bed sensor (β=−0.03, 95% CI −0.06 to 0.00, P=.032). Patients with bipolar/ borderline personality disorder showed lower TST alignment, and alignment between smartphone and bed sensor was worse in females (β = −1.03, 95% CI −1.74 to −0.33, p = .004). Longer daylight duration was also associated with improved alignment in sleep offset and TST.
Conclusions:
This study demonstrates the feasibility of using actigraphy, smartphone data, and bed sensors for sleep tracking in naturalistic settings with patients. It highlights measurement biases across devices, the impact of seasonal variations on sleep research in unique geographical regions like Finland, and key demographic factors influencing sleep measurement discrepancies.
Citation
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Copyright
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