Predictive Progressive Factors of Adolescent Idiopathic Scoliosis
NCT ID: NCT02862392
Last Updated: 2025-09-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
95 participants
OBSERVATIONAL
2017-03-15
2024-12-04
Brief Summary
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Detailed Description
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AIS is progressive (in 3 out of 10 cases) when the scoliosis radiographic frontal angle (Cobb angle) strictly increases by 5° between the diagnosis date and the end of growth. This progression can be severe requiring heavy treatments (corset, surgery) and it can generate adverse effects (spine pain, cardio-respiratory and functional consequences on walking). The lack of reliable criteria to predict the evolution of AIS is a real problem for the therapeutic decision and it can impact the socio-economic cost of the disease.
Several studies show orthostatic postural control anomalies in AIS. The orthostatic postural control is elaborated from the central integration of different sensorial signals (visual, somesthesic and vestibular).
Posturography, on computerized integrate force plates, allows to quantify sensorial components of orthostatic postural control. This technique can confirm the disorders of orthostatic postural control in AIS, but the parameters used can not evaluate with precision the progressive potential.
The posturographic signal analysis could lead to the implementation of therapeutic strategies adapted to progressive risk. Moreover, this method could prevent the progression in major scoliosis, limit the use of radiography, the application of a constraining corset (worn 23 hours a day) and the possibility of heavy surgery (extent arthrodesis).
The hypothesis of this study is that progressive AIS is characterized by a disorder of orthostatic postural control. The analysis and the treatment of posturographic signal on computerized integrate force plates, coupled to clinical and radiographic examinations, could highlight predictive and reliable factors at the moment of diagnosis. Thus, it could help the clinician in his therapeutic approach, based on the postural control improvement (individualized prescription in kinesitherapy, better adaptation to orthopedic treatments by corset). This method is non-invasive, without side effects, fast and achievable in routine care at the moment of the diagnosis of AIS.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patient with AIS, associated with a frontal deviation of spine measured by the radiographic frontal angle of Cobb between 15° and 20°, and a spinal rotation attested by the presence of a gibbosity minimum 5° with Bunnell scoliometer.
* Risser test \< 2 (evaluation of the spine bone maturity)
* Patient having front and side views radiographies from spine (huge prints) of less than three months (children have a radiographic check-up from total spine every 6 months on average, no additional print is requested)
* Capable of receiving clear informations
* Giving a written consent for their participation via a consent signed by both parents of the patient (or legal tutor)
* Covered by a healthcare insurance
Exclusion Criteria
* AIS with principal cervico-thoracic curve, according to the Scoliosis Research Society (SRS) classification (this patient category only represents 1% of SIA)
* Primary left thoracic topographic AIS, according to the SRS classification (this category of scoliosis is rare and frequently has a secondary origin: neurologic, polymalformative)
* AIS treated by corrective corset
* Length inequality between inferior members more than 20 mm during clinical examination
* Patient with clinical neurological signs
* Pathological ligamentous laxity
* Known vestibular disease
* BMI \> 30
* Refusal to sign an informed consent
* Impossibility to receive clear information
11 Years
14 Years
FEMALE
No
Sponsors
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Ecole des hautes études d'ingénieur (HEI)
UNKNOWN
Lille Catholic University
OTHER
Responsible Party
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Principal Investigators
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Catanzariti Jean-François, MD
Role: PRINCIPAL_INVESTIGATOR
Lille Catholic University
Olivier Agnani
Role: STUDY_CHAIR
Lille Catholic University
Locations
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Fondation Hopale
Berck, Hauts-de-France, France
Centre de MPR pour enfants de Bois Larris
Lamorlaye, Hauts-de-France, France
SSR pédiatrique Marc Sautelet
Villeneuve-d'Ascq, Hauts-de-France, France
CHU d'Amiens
Amiens, Picardie, France
Countries
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Other Identifiers
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RC-P0047
Identifier Type: -
Identifier Source: org_study_id
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