Evidence map›Paper›PMID 41041018›Full record

ArticleFrontiers in human neuroscience2025

Clinical Gait Evaluation with Neuromuscular Impairments (Clinical GENI) for spastic cerebral palsy.

Kylie Clewes, Yiwen Dong, Mary Meyer, Evan Lowe, Kornél Schadl, Jessica Rose

Abstract read
In one paragraph

Article in Frontiers in human neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Review
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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.

Kylie ClewesMotion & Gait Analysis Lab, Lucile Packard Children's Hospital, Stanford Medicine Children's Health, Palo Alto, CA, United States.
Yiwen DongMotion & Gait Analysis Lab, Lucile Packard Children's Hospital, Stanford Medicine Children's Health, Palo Alto, CA, United States.
Mary MeyerMotion & Gait Analysis Lab, Lucile Packard Children's Hospital, Stanford Medicine Children's Health, Palo Alto, CA, United States.
Evan LoweMotion & Gait Analysis Lab, Lucile Packard Children's Hospital, Stanford Medicine Children's Health, Palo Alto, CA, United States.
Kornél SchadlMotion & Gait Analysis Lab, Lucile Packard Children's Hospital, Stanford Medicine Children's Health, Palo Alto, CA, United States.
Jessica RoseMotion & Gait Analysis Lab, Lucile Packard Children's Hospital, Stanford Medicine Children's Health, Palo Alto, CA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gait abnormalities in spastic cerebral palsy (CP) result from four primary neuromuscular impairments: muscle weakness, short muscle-relative-to-skeletal-length, muscle spasticity, and impaired selective motor control. The Clinical Gait Evaluation with Neuromuscular Impairments (Clinical GENI) was developed to help clinicians identify gait abnormalities and contributing neuromuscular impairments in spastic CP for use in any clinical setting. Aims: This study evaluated use and validity of the observational-based Clinical GENI to identify gait abnormalities and contributing neuromuscular impairments in children with spastic CP. Methods: Patients with spastic CP seen in 2023 for instrumented gait analysis and physical exam of neuromuscular impairments were evaluated using the Clinical GENI. Validity was assessed by agreement between identification of gait abnormalities on the Clinical GENI compared to 3D gait kinematics. Severity of neuromuscular impairments associated with gait abnormalities listed on the Clinical GENI was compared, and severity of neuromuscular impairment was correlated with severity of gait abnormalities. Results: Participants included 12 children with spastic CP (4 GMFCS I, 8 GMFCS II; mean age 11.25 years). The most common gait abnormalities were forefoot/flatfoot initial contact (IC) (16/24), flexed-knee IC (19/24), hip-flexion in single limb stance (12/24), and reduced pre-swing ankle plantarflexion (19/24). Strong agreement (83-100%) occurred between gait abnormalities on the Clinical GENI and kinematic values. Severity of neuromuscular impairment was higher ( Conclusion: Results support clinical utility and validity of the Clinical GENI for evaluating gait abnormalities and contributing neuromuscular impairments in spastic CP.

Indexed as

cerebral palsygait analysisimpaired selective motor controlmuscle weaknessneuromuscular impairmentsshort muscle-tendon unitspasticity

Identifiers

PMID41041018
PMCPMC12484064

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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.