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Study identifier: NCT06320288 Synced from ClinicalTrials.gov · July 29, 2026
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Analysis of Trunk and Center of Mass Control Development During Gait in Children With Cerebral Palsy (VERTEBRAL)

Condition: Children With Cerebral Palsy  ·  Sponsor: Union de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est

PhaseN/A
Planned participants270
Who can joinAll sexes, 18 Months to 18 Years
Healthy volunteersYes

About this study

During the acquisition of posturokinetic abilities such as walking, postural control of the trunk is of paramount importance. Indeed, its development is strongly linked to the overall motor function of children. In cerebral palsy (CP), a term that refers to a set of motor disorders following a perinatal lesion, deficits in axial control are present from early childhood. These deficits are strongly correlated with the functional deficits observed in this population. In particular, during walking, deviations of the trunk (amplitudes, accelerations) are observed in the three planes of space. While recent literature increasingly questions the impact of trunk control deficit on the walking of children with CP, elements are still missing for a holistic understanding of the interaction between locomotor and postural disorders in children with CP. In particular, no study has focused on the deviations of trunk control and the center of mass (which is a global indicator of balance strategies) during the development and maturation of walking in children with CP. Therefore, the primary objective of this cross-sectional observational study will be to characterize the development of trunk control and center of mass during walking in children with CP.

This description comes directly from the study's public registry record.

Talk to the study team

Jonathan Pierret, PhD  ·  +33 3 82 52 6761  ·  jonathan.pierret@ugecam.assurance-maladie.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Institut Régional de Médecine Physique et de RéadaptationNancy, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06320288