Evidence map›Paper›PMID 40474269›Full record

SynthesisJournal of neuroengineering and rehabilitation2025

Outcome measures of instrumented gait analysis in hereditary spastic paraplegia: a systematic review.

Veronika Koch, Alzhraa Ibrahim, Juergen Winkler, Bjoern Eskofier, Martin Regensburger, Heiko Gassner

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of neuroengineering and rehabilitation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Hereditary spastic paraplegia: from decades of therapy to future innovations.Therapeutic advances in neurological disorders · 2026
    Review
  3. A novelFrontiers in neuroscience · 2025
    Article
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

6 authors.

Veronika KochFraunhofer Institute for Integrated Circuits IIS, Erlangen, Germany.ORCID http://orcid.org/0000-0002-2246-7686
Alzhraa IbrahimDepartment of Molecular Neurology, University Hospital Erlangen, Friedrich-Alexander-Universität, Erlangen-Nürnberg (FAU), Erlangen, Germany.
Juergen WinklerDepartment of Molecular Neurology, University Hospital Erlangen, Friedrich-Alexander-Universität, Erlangen-Nürnberg (FAU), Erlangen, Germany.ORCID http://orcid.org/0000-0003-0630-9204
Bjoern EskofierMachine Learning and Data Analytics Lab, Department Artificial Intelligence in Biomedical, Engineering (AIBE), Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.ORCID http://orcid.org/0000-0002-0417-0336
Martin RegensburgerDepartment of Molecular Neurology, University Hospital Erlangen, Friedrich-Alexander-Universität, Erlangen-Nürnberg (FAU), Erlangen, Germany.ORCID http://orcid.org/0000-0002-2172-7386
Heiko GassnerFraunhofer Institute for Integrated Circuits IIS, Erlangen, Germany. heiko.gassner@uk-erlangen.de.ORCID http://orcid.org/0000-0003-2037-9460

Funding

Deutsche Forschungsgemeinschaft (DFG) collaborative research center EmpkinS CRC 1483EU-wide ERAPerMed project DIGIPD 01KU2110Fraunhofer Internal Programs Attract 044-602140TreatHSP consortium 01GM2209B
6 · The paper itself

Abstract

backgroundHereditary spastic paraplegias (HSPs) comprise a group of genetic movement disorders characterized by progressive spasticity and weakness of the lower limbs leading to gait deficits. Instrumented gait measures are applied to quantify gait patterns in HSP objectively. However, there is no consensus on the most relevant HSP-specific digital outcome measures for future clinical studies.

aimThis systematic review aims to summarize outcome measures of instrumented gait analysis in HSP patients, focusing on both traditional motion capture (MOCAP) and inertial sensor systems.

methodsFollowing PRISMA-2020 guidelines, a comprehensive literature search was conducted in PubMed, Scopus, and Web of Science to identify studies using instrumented gait analysis in HSP. Data on participant characteristics, measurement systems, outcome measures, results, and risk of bias were systematically extracted.

resultsIn total, 38 studies published between 2004 and 2024, including 29 observational studies and 9 interventional studies, met the inclusion criteria. Various gait parameters were used, including spatio-temporal, kinematic, kinetic, and electromyography (EMG) parameters. Walking speed and range-of-motion (ROM) knee were identified as important parameters for differentiating HSP patients from healthy controls, but these parameters are more general rather than disease-specific. Foot lift, ROM foot, and gait variability are promising, more disease-specific parameters, as they reflect disease severity and increased balance deficits. However, a deeper understanding of all gait parameter categories is necessary, particularly for the upper body. Few studies explored sub-cohorts that exhibit different HSP gait characteristics.

conclusionWhile MOCAP provides valuable data in controlled hospital environments, there is a need for validated mobile sensor systems capturing the gait patterns of HSP patients in real-life without supervision. Future research must focus on better longitudinal multicenter studies with larger sample sizes to establish robust digital outcomes and monitor disease progression and therapeutic response in HSP.

Indexed as

Gait AnalysisGait Disorders, NeurologicOutcome Assessment, Health CareSpastic Paraplegia, HereditaryBiomechanical PhenomenaHumansRange of Motion, ArticularGait analysisHereditary spastic paraplegiasInertial measurement unitMobile sensor systemsMotion captureSensors

Identifiers

PMID40474269
PMCPMC12139076

What OpenQuestion holds

Textmetadata
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.