Evidence map›Paper›PMID 42818789›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Smartwatch-derived digital biomarkers distinguish episodic pain phenotypes in chronic low back pain.

Karim Khattab, Aniket Pratapneni, Gregorij Kurillo, Trisha Hue, Patricia Zheng, Jeffrey Lotz, Abel Torres-Espin, Jeannie F Bailey, REACH Investigators

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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
–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

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

9 authors.

Karim KhattabDepartment of Orthopaedic Surgery, University of California San Francisco, San Francisco, USA.
Aniket PratapneniDepartment of Orthopaedic Surgery, University of California San Francisco, San Francisco, USA.ORCID 0009-0002-7293-098X
Gregorij KurilloDepartment of Orthopaedic Surgery, University of California San Francisco, San Francisco, USA.
Trisha HueDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, USA.
Patricia ZhengDepartment of Orthopaedic Surgery, University of California San Francisco, San Francisco, USA.
Jeffrey LotzDepartment of Orthopaedic Surgery, University of California San Francisco, San Francisco, USA.
Abel Torres-EspinDepartment of Neurological Surgery, University of California San Francisco, San Francisco, USA.
Jeannie F BaileyDepartment of Orthopaedic Surgery, University of California San Francisco, San Francisco, USA.ORCID 0000-0003-4618-7512
REACH Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic low back pain affects over half a billion people globally and is the leading cause of disability worldwide, yet objective tools for characterizing how individual patients experience pain over time remain lacking. Patients with chronic low back pain exhibit distinct pain trajectory patterns: some experience relatively stable pain while others experience episodic fluctuations with flare-ups. These trajectories have been found to be clinically meaningful but are currently captured only through subjective self-report. Consumer smartwatches offer an opportunity for passive, continuous, objective monitoring of physiological and behavioral signals that may reflect these fluctuations. We evaluated whether temporal features extracted from six months of smartwatch-derived resting heart rate, heart rate variability, and step count data could discriminate between episodic and non-episodic pain phenotypes in 261 chronic low back pain patients from a longitudinal observational cohort. We applied stability-selected elastic-net logistic regression models to temporal features and evaluated model performance using nested cross-validation and SHAP-based feature importance analysis. Summary statistics showed no significant differences between pain groups across any signal modality. Functional principal component analysis revealed high temporal heterogeneity in trajectories of resting heart rate, heart rate variability, and step count. Temporal trajectory models substantially outperformed summary-based approaches, with a models achieving areas under the receiver operating curve ranging from 0.66 to 0.82. Frequency-domain features and local variability measures drove classification performance, and combining heart rate and activity features provided complementary discriminative information, performing better than models trained on any subset of modalities. These findings demonstrate the feasibility of passively collected smartwatch data as objective digital biomarkers for pain phenotyping in chronic low back pain, establishing a methodological approach that may permit personalized pain management through objective monitoring of patient pain and response to intervention.

Identifiers

PMID42818789
PMCPMC13622701

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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.