Evidence map›Paper›PMID 41079689›Full record

ArticleFrontiers in digital health2025

Enhancing ALS progression tracking with semi-supervised ALSFRS-R scores estimated from ambient home health monitoring.

Noah Marchal, William E Janes, Sheila Marushak, Mihail Popescu, Xing Song

Abstract read
In one paragraph

Article in Frontiers in digital health, 2025. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Noah MarchalInstitute for Data Science and Informatics, University of Missouri, Columbia, MO, United States.
William E JanesDepartment of Occupational Therapy, University of Missouri, Columbia, MO, United States.
Sheila MarushakDepartment of Occupational Therapy, University of Missouri, Columbia, MO, United States.
Mihail PopescuInstitute for Data Science and Informatics, University of Missouri, Columbia, MO, United States.
Xing SongInstitute for Data Science and Informatics, University of Missouri, Columbia, MO, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Clinical monitoring of functional decline in amyotrophic lateral sclerosis (ALS) relies on periodic assessments, which may miss critical changes that occur between visits when timely interventions are most beneficial. Methods: To address this gap, semi-supervised regression models with pseudo-labeling were developed; these models estimated rates of decline by targeting Revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R) trajectories with continuous in-home sensor data from a three-patient ALS case series. Three model paradigms were compared (individual batch learning and cohort-level batch vs. incremental fine-tuned transfer learning) across linear slope, cubic polynomial, and ensembled self-attention pseudo-label interpolations. Results: Results showed cohort-level homogeneity across functional domains. For ALSFRS-R subscales, transfer learning reduced the prediction error in 28 of 34 contrasts [mean root mean square error (RMSE) = 0.20 (0.14-0.25)]. However, for composite ALSFRS-R scores, individual batch learning was optimal for two of three participants [mean RMSE = 3.15 (2.24-4.05)]. Self-attention interpolation best captured non-linear progression, providing the lowest subscale-level error [mean RMSE = 0.19 (0.15-0.23)], and outperformed linear and cubic interpolations in 21 of 34 contrasts. Conversely, linear interpolation produced more accurate composite predictions [mean RMSE = 3.13 (2.30-3.95)]. Distinct homogeneity-heterogeneity profiles were identified across domains, with respiratory and speech functions showing patient-specific progression patterns that improved with personalized incremental fine-tuning, while swallowing and dressing functions followed cohort-level trends suited for batch transfer modeling. Discussion: These findings indicate that dynamically matching learning and pseudo-labeling techniques to functional domain-specific homogeneity-heterogeneity profiles enhances predictive accuracy in tracking ALS progression. As an exploratory pilot, these results reflect case-level observations rather than population-wide effects. Integrating adaptive model selection into sensor platforms may enable timely interventions as a method for scalable deployment in future multi-center studies.

Indexed as

amyotrophic lateral sclerosisdisease progressionfunctional statuspatient monitoringpersonalized medicineremote sensing technologysemi-supervised machine learning

Identifiers

PMID41079689
PMCPMC12511069

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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.