Postural Balance of the Adult (POSTURADULT)

May 6, 2013 updated by: University Hospital, Bordeaux

3D Evaluation of Postural Balance of the Adult Affected by Postural Trouble, Using EOS™ Images and 3D-reconstructions With Regard to Gravity Line.

Description of the geometrical configuration of the skeleton with regard to gravity line by patients suffering from spinal disorders that may induce postural troubles

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

In clinical routine, 3D analysis of postural balance is only made using clinical examination. When dealing with specific pathologies, in particular spine disorders, a better understanding of the balance could help better treat and prevent late complications. This prospective study aims at describing the pathologies of the musculoskeletal system using 3D reconstruction of the spine, the pelvis and the inferior limbs with regard to gravity line by patients suffering from postural trouble and defining new parameters to assess postural balance

Study Type

Interventional

Enrollment (Actual)

26

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Bordeaux, France, 33076
        • Unité de Pathologie Rachidienne Tripode CHU Pellegrin, Place Amélie Raba-Léon

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Affiliated to social insurance
  • Informed of the benefits, the risks and the conduction of the study and have given their free informed consent.

For Patients

  • Medical prescription for an EOS™ exam, or for Frontal AND Lateral full-spine radiographs or for a pangonogram.

For Healthy Volunteers

  • 50 years old

Exclusion Criteria:

For Patients

  • Patients that neither need any EOS™ exam, nor Face & Lateral full-spine radiographs, nor pangonogram.

For Healthy Volunteers

  • Children or young adults (<50)
  • Psychiatric or neurologic deficit.
  • Anterior Surgery of Spine or inferior Member
  • Chronic back pain
  • Recent acute back Pain

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Healthy volunteers
Small group of aged healthy volunteers
Double Incidence Postero Anterior and Lateral full body low-dose X-ray acquisition on EOS™ device following SOP of the service of radiology.
Other: Patients
Patients consulting for spine disorders that may or may not have postural troubles
Double Incidence Postero Anterior and Lateral full body low-dose X-ray acquisition on EOS™ device following SOP of the service of radiology.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
To assess the three-dimensional geometrical configuration of the skeleton with respect to the gravity line on a large population of patient presenting a broad spectrum of pathologies inducing postural imbalance.
Time Frame: 1 day
1 day

Secondary Outcome Measures

Outcome Measure
Time Frame
3D Position of the middle of acoustic meati, of each vertebral body, of the center of both acetabula and the barycentre of the four condyles with respect to the gravity line.
Time Frame: 1 day
1 day
Morphologic and positioning parameters of the pelvis (pelvic incidence, pelvic version, sacral slope & pelvic radius)
Time Frame: 1 day
1 day
Kyphosis, lordosis and sinopelvic balance
Time Frame: 1 day
1 day
To validate the measure of femoral and tibial torsion using EOS™ images
Time Frame: 1 day
1 day
influence of position change on the evaluation of changes in postural balance following surgery
Time Frame: After surgery
After surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Jean-Marc VITAL, Professor, Hospital University, Bordeaux
  • Study Director: Wafa SKALLI, PhD, Pr, Laboratoire de Biomécanique Arts et Metiers ParisTech-CNRS UMR 8005

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2009

Primary Completion (Actual)

December 1, 2010

Study Completion (Actual)

December 1, 2010

Study Registration Dates

First Submitted

June 18, 2009

First Submitted That Met QC Criteria

June 22, 2009

First Posted (Estimate)

June 23, 2009

Study Record Updates

Last Update Posted (Estimate)

May 7, 2013

Last Update Submitted That Met QC Criteria

May 6, 2013

Last Verified

May 1, 2013

More Information

Terms related to this study

Other Study ID Numbers

  • CHUBX 2008/32

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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