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MOUVSCO: Kinematic Analysis of the Trunk in Patients With Moderate Scoliosis

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status

Terminated

Conditions

Scoliosis

Treatments

Other: Data recording with all sensors

Study type

Interventional

Funder types

Other
NETWORK

Identifiers

NCT02134704
MOUVSCO-DCIC-1411

Details and patient eligibility

About

The hypothesis of this study is that moderate scoliosis patients have postural and kinematic differences (static and dynamic) compared with healthy volunteers and it is possible to characterize and quantify.

The aim of this study is the detailed analysis of postural anomalies in moderate scoliosis patients compared with healthy volunteers

Full description

Subjects participating in the study must wear sensors that will be arrange at the shoulders, spine, pelvis and legs. Subjects will perform under the direction of the investigator, different tasks of a total duration of 45 minutes.

During the period of experimentation, the data collected will be:

  • the positions of each one of the sensors in all three planes of space,
  • the ground support forces

Enrollment

48 patients

Sex

Female

Ages

9 to 16 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Scoliosis Group - Inclusion Criteria:

  • female children patients from 9 to 16 years old,
  • patients with idiopathic scoliosis lumbar left and / or right thoracic,
  • patients with moderate scoliosis: Cobb angle measured on a radiograph between 10 ° and 25°,
  • both parents of patients must be affiliated to social security or similarly regime.

Healthy Volunteers Group - Inclusion Criteria:

  • female children from 9 to 16 years old, matched in age and size with scoliosis patients,
  • children with no neuromuscular disease that may have an influence on the required tasks,
  • both parents of children must be affiliated to social security or similarly regime,

Exclusion Criteria:

  • refusal to consent: from child's in age to consent or from both parents

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

48 participants in 2 patient groups

Scoliosis Group
Experimental group
Treatment:
Other: Data recording with all sensors
Healthy Volunteers Group
Experimental group
Treatment:
Other: Data recording with all sensors

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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