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TerminatedNCT02134704MOUVSCOUpdated Aug 30, 2016

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

An interventional study of Data recording with all sensors in Scoliosis, sponsored by University Hospital, Grenoble. Terminated at 1 site in France. Open to female participants aged 9 Years to 16 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-08-30.

Sponsored by University Hospital, Grenoble · Not applicable, Interventional, and Basic science

Why this study was terminated
All patients were recruted but it has been difficulte to recrute all volunteers (15/30) . However data should be sufficient for analyse of data.
Phase
Not applicable
Study type
Interventional
Enrollment
48
Allocation
Non-randomized
Ages
9 Years to 16 Years
Sex
Female
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Study summary

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

Read the detailed 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
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Conditions studied

  • Scoliosis

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03

In context

Scoliosis

593 studies on the registry are indexed under Scoliosis; 138 are open to participants now.

This study's enrollment of 48 is close to the median of 44 across 344 interventional studies indexed under Scoliosis.

Browse Scoliosis studies →

Lead sponsor

University Hospital, Grenoble is the lead sponsor of 815 studies on the registry; 205 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
9 Years to 16 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Eligibility 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
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
48 participants (actual)

Study arms

  • Experimental
    Scoliosis Group

    Other: Data recording with all sensors

  • Experimental
    Healthy Volunteers Group

    Other: Data recording with all sensors

Interventions

  • OtherData recording with all sensors

    The sensors will be placed in the child body and will allow the collection of all the data of the trial.

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What researchers measure

Primary outcomes

  1. Relative movements, in mm, of the spinous processes in the three planes of space

    Characterize the kinematic anomalies in scoliosis patients compared with healthy volunteers during typical tasks of trunk flexion.

    Time frame: 2 hours

Secondary outcomes

  1. Relative rotations of the bi-acromial line, thoracic and pelvic plan.

    * Assess the existence of kinematic differences between the scoliosis patients and healthy volunteers during forward bending. * Assess the kinematic differences between the scoliosis patients and healthy volunteers when they sit and up from a stool. * Assess the kinematic differences between the scoliosis patients and healthy volunteers during walking.

    Time frame: 2 hours

  2. Walking speed, step length and single stance time.

    Assess the performance of walking in scoliosis patients.

    Time frame: 2 hours

  3. The surface of displacement of the center of plantar pressure, static relative orientation of the bi-acromial line, thoracic and pelvic plan.

    Assess balance and static posture of scoliotic patients.

    Time frame: 2 hours

07

Study locations

1 site
  • Émilie Chipon
    Grenoble, Isère 38043, France
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 30, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02134704
Lead sponsor
University Hospital, Grenoble
Collaborators
TIMC-IMAG, Clinical Investigation Centre for Innovative Technology Network
Responsible party
Sponsor
First posted
May 9, 2014
Start date
Sep 2014
Primary completion
Jun 2016
Completion
Jun 2016
Last update
Aug 30, 2016

Study contacts

Aurelien Courvoisier, Pr
principal investigator · University Hospital, Grenoble

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

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