ArticleNPJ digital medicine2026
Identifying unique gait phenotypes across neuromotor conditions using wearable inertial sensors and topological data analysis.
Article in NPJ digital medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Wearable sensors quantify gait and mobility in detail, but translating high-dimensional data into clinically actionable insights remains challenging in precision rehabilitation. We applied Topological Data Analysis (TDA) to inertial sensor recordings from multiple gait assessments in 81 individuals with stroke, Parkinson's disease, lower-limb difference, functional neurological disorders, and healthy controls. TDA generated a unified functional map that organized participants based on shared gait patterns across conditions. Within stroke, three phenotypes, corresponding to low, moderate, and high gait function emerged and aligned with clinical outcomes, while Parkinson's disease shows a smoother transition from low- to high-function phenotypes. Individuals with lower-limb difference were distributed across other conditions which reflected their variable and shared gait patterns. Supervised machine-learning analysis further identified gait signatures for each phenotype. This framework enables mapping new patients into interpretable functional phenotypes, supports targeted intervention planning, and permits clinical decision-making from sensor data.
Identifiers
42393385What OpenQuestion holds
Registered trials
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.