Evidence map›Paper›PMID 42856621›Full record

ArticlebioRxiv : the preprint server for biology2026

Deep learning models detect neuromuscular disease and quantify functional impairment from video-derived biomechanics data.

Sydney C Covitz, Parker S Ruth, Shelby Vogt-Domke, Carmichael Ong, Tian Tan, Audrey Chun, Sarah Ismail, Lin Karman, Julie Muccini, Shannon Li and 7 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

17 authors.

Sydney C CovitzDepartment of Bioengineering, Schools of Engineering & Medicine, Stanford University, Stanford, CA.ORCID 0000-0002-7430-4125
Parker S RuthDepartment of Computer Science, School of Engineering, Stanford University, Stanford, CA.ORCID 0000-0003-1030-4916
Shelby Vogt-DomkeDepartment of Neurology, Stanford Medicine, Stanford, CA.ORCID 0009-0000-0422-2848
Carmichael OngDepartment of Bioengineering, Schools of Engineering & Medicine, Stanford University, Stanford, CA.ORCID 0000-0002-0589-5347
Tian TanDepartment of Bioengineering, Schools of Engineering & Medicine, Stanford University, Stanford, CA.ORCID 0000-0003-4639-8301
Audrey ChunDepartment of Neurology, Stanford Medicine, Stanford, CA.ORCID 0009-0004-9350-5207
Sarah IsmailDepartment of Neurology, Stanford Medicine, Stanford, CA.ORCID 0009-0003-6719-1286
Lin KarmanDepartment of Neurology, Stanford Medicine, Stanford, CA.ORCID 0009-0002-7645-620X
Julie MucciniDepartment of Radiology, Stanford Medicine, Stanford, CA.ORCID 0000-0001-6118-4999
Shannon LiDepartment of Mechanical Engineering, School of Engineering, Stanford, CA.ORCID 0009-0009-9840-2342
Melina RogersDepartment of Neurology, Stanford Medicine, Stanford, CA.ORCID 0009-0001-0526-8167
Scott UhlrichDepartment of Mechanical Engineering, University of Utah, Salt Lake City, Utah.ORCID 0000-0002-3113-367X
John W DayDepartment of Neurology, Stanford Medicine, Stanford, CA.ORCID 0000-0002-0086-9529
Jennifer L HicksDepartment of Bioengineering, Schools of Engineering & Medicine, Stanford University, Stanford, CA.ORCID 0000-0002-2516-9334
Constance de MontsDepartment of Neurology, Stanford Medicine, Stanford, CA.ORCID 0009-0004-7659-8069
Tina DuongDepartment of Neurology, Stanford Medicine, Stanford, CA.ORCID 0000-0003-3177-4722
Scott L DelpDepartment of Bioengineering, Schools of Engineering & Medicine, Stanford University, Stanford, CA.ORCID 0000-0002-9643-7551

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Measurements of human movement are critical for evaluating patients with neuromuscular diseases. However, current clinical tools are limited in sensitivity and can fail to detect the full spectrum of movement changes patients may exhibit. These limitations can obscure early signs of decline, delaying interventions that could preserve function and independence. OpenCap-a smartphone application that performs video-based markerless motion capture-can help address this gap by enabling scalable, out-of-lab measurements of human movement. Here, we present a method for both detecting disease and quantifying the severity of impaired movement from smartphone videos of a patient's motion. We used OpenCap to measure kinematics from 337 individuals with diagnoses spanning 12 rare, genetically-defined neuromuscular diseases and 78 age-matched healthy controls. Our dataset is the largest existing publicly available resource of body segment kinematics for this class of diseases. These data were collected in neuromuscular clinics during regular clinic visits as well as at conferences and community events across the United States. We trained deep learning models on these kinematic time series to differentiate between participants with neuromuscular disease and controls (AUROC = 0.97 [0.93-1.00]). We also developed a movement impairment severity score that correlates with both participants' ratings of their own functional abilities (ρ= -0.81, p<0.001) and existing clinical tests of movement capabilities such as run speed (ρ= -0.83, p<0.001). Our methods for detecting disease and deriving quantitative biomarkers of movement impairment from smartphone videos have the potential to complement clinical assessments, inform screening protocols, and improve clinical trial endpoints.

Identifiers

PMID42856621
PMCPMC13648720

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.