Evidence map›Paper›PMID 40432027›Full record

ArticleSensors (Basel, Switzerland)2025

Harnessing Fast Fourier Transform for Rapid Community Travel Distance and Step Estimation in Children with Duchenne Muscular Dystrophy.

Erik K Henricson, Albara Ah Ramli

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

2 authors.

Erik K HenricsonDepartment of Physical Medicine and Rehabilitation, School of Medicine, University of California, Davis, 1 Shields Ave., Davis, CA 95616, USA.ORCID 0000-0002-7511-6441
Albara Ah RamliDepartment of Physical Medicine and Rehabilitation, School of Medicine, University of California, Davis, 1 Shields Ave., Davis, CA 95616, USA.ORCID 0000-0002-4617-225X

Funding

Muscular Dystrophy Association 646805U.S. Department of Defense W81XWH-17-1-0477
6 · The paper itself

Abstract

Accurate estimation of gait characteristics, including step length, step velocity, and travel distance, is critical for assessing mobility in toddlers, children, and teens with Duchenne muscular dystrophy (DMD) and typically developing (TD) peers. This study introduces a novel method leveraging Fast Fourier Transform (FFT)-derived step frequency from a single waist-worn consumer-grade accelerometer to predict gait parameters efficiently. The proposed FFT-based step frequency detection approach, combined with regression-derived stride length estimation, enables precise measurement of temporospatial gait features across various walking and running speeds. Our model, developed from a diverse cohort of children aged 3-16, demonstrated high accuracy in step length estimation (R2=0.92, RMSE=0.06 m) using only step frequency and height as inputs. Comparative analysis with ground-truth observations and AI-driven Walk4Me models validated the FFT-based method, showing strong agreement across step count, step frequency, step length, step velocity, and travel distance metrics. The results highlight the feasibility of using widely available mobile devices for gait assessment in real-world settings, offering a scalable solution for monitoring disease progression and mobility changes in individuals with DMD. Future work will focus on refining model performance and expanding applicability to additional movement disorders.

Indexed as

GaitMuscular Dystrophy, DuchenneAccelerometryAdolescentChildChild, PreschoolFemaleFourier AnalysisHumansMaleWalkingcommunity ambulationdigital biomarkersDuchenne muscular dystrophyFast Fourier Transformgait analysisinertial measurement unit (IMU)machine learningmobile health (mHealth)step frequencystep length estimationwearable sensors

Identifiers

PMID40432027
PMCPMC12115490

What OpenQuestion holds

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LicenceCC BY
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.