Investigating Proprioceptive Impairment in Adolescents With Idiopathic Scoliosis (AIS) (SCOLIO-PROPRIO)

Official title

Investigating Proprioceptive Impairment in Adolescents With Idiopathic Scoliosis (AIS)

Overview

The goal of this interventionnal study is to learn if teenagers who have severe scoliosis (a curvature of the spine) have trouble sensing their body's position in space (this sense is called proprioception), which are directly linked to abnormalities in the part of the brain that controls movement and/or caused by the muscles on each side of the spine not being the same size or not developing in the same way. The main question the investigators aim to answer are : * Do adolescents with severe scoliosis have problems with their sense of body position (proprioception)? * If so, are these proprioceptive issues linked to specific problems in the part of the brain that controls movement? * Are these proprioceptive issues also possibly linked to an uneven muscle structure on either side of the spinal curve? Researchers will compare the part of the brain that controls movement (ensorimotor brain network) of healthy subjects to that of the participants that will enroll in this study. Participants will only have to do one more MRI that is not included in the routine of clinical management of scoliosis before surgery. Data will also be retrieved from clinical practice Participants will answer questionnaires after the day of the surgery

Detailed description

Adolescent Idiopathic Scoliosis (AIS) affects 2 to 4% of the pediatric population. While its exact etiology remains unclear, one leading hypothesis implicates deficits in muscle proprioception, though this remains poorly understood. In addition, structural and functional alterations in brain connectivity have been reported in AIS patients, raising the possibility of a neurobiological underpinning linked to proprioceptive dysfunction.

The primary objective of this study is to determine whether adolescents with severe AIS requiring surgical treatment exhibit structural alterations in the brain's sensorimotor network compared to age-matched control subjects, and whether these alterations are associated with their level of proprioceptive sensitivity. A secondary objective is to assess whether resting-state functional connectivity within the sensorimotor network is also disrupted in AIS patients and whether these functional changes correlate with proprioceptive performance.

The investigators will combine behavioral assessments of static and dynamic proprioception with structural (diffusion MRI) and functional (resting-state fMRI) neuroimaging (using MR scanner at 3T). Static proprioception will be assessed using a joint repositioning test, while dynamic proprioception will be evaluated through vibration-induced movement illusions. This is a prospective, single-center study involving 30 AIS patients and 30 age- and gender-matched healthy controls drawn from open-access neuroimaging databases.

Demonstrating a correlation between brain network alterations and proprioceptive deficits in AIS would provide new evidence in favor of a neuroproprioceptive origin of scoliosis. Such findings could pave the way for the development of targeted proprioceptive rehabilitation strategies in affected adolescents.

Interventions

• Radiation MRI
  Brain and Spinal Cord MRI

Primary outcome measures

• Correlation between scoliosis and structural brain alteration as assed by dynamic proprioception test and MRI [Time frame: One day before surgery]

Secondary outcome measures (5)

• Resting state functional connectivity (rs-FC) alteration in AIS assed by MRI [Time frame: One day before surgery]
• Correlation between Resting-State Functional Connectivity (z-score) as assessed from brain MRI's and Proprioceptive Performance as assessed by measuring the Reproduced Leg Extension Amplitude in degres (°) [Time frame: Day before surgery]
• Correlation between scoliosis gravity as assessed by the cobb angle (°) with previous MRI's and propriovceptive performance as assessed by measuring the Reproduced Leg Extension Amplitude in degres (°) and the quantified gait analysis (°) [Time frame: One day before surgery]
• Analysis of scores on body perception as assed by the BESAA [Time frame: From day one after surgery to 14 day after surgery]
• Physical activity as assessed by the Physical Effort Scale (PES) correlated with cobb angle [Time frame: From day one after surgery to 14 day after surgery]

Eligibility criteria

Inclusion criteria

• Adolescents diagnosed with Adolescent Idiopathic Scoliosis (AIS) and followed in the pediatric orthopedic surgery department, scheduled to undergo spinal fusion surgery (arthrodesis)
• No history or clinical signs of neurological disorders
• Aged between 10 and 18 years
• Written informed consent obtained from both the adolescent and their legal guardians (parents)
• Control Group only: Participants will be selected from open-access neuroimaging databases, matched to the patient group by age and sex.

Exclusion criteria

• Presence of any other clinically significant condition that could be associated with spinal deformity
• Insufficient proficiency in French to understand the informed consent form
• Current treatment with psychotropic medication
• Ongoing pregnancy or breastfeeding
• Subject under legal or judicial supervision
• Contraindications to brain MRI (including: pacemaker; electrically, magnetically, or mechanically activated implants; surgical clips; metallic sutures; staples; etc. - see MRI safety questionnaire annex)
• Subject or their parent(s)/legal guardian(s) refuse to be informed of incidental findings detected during MRI
• Claustrophobia

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Non-randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Other

Study locations

France · 1 center

• Assistance Publique Hôpitaux de Marseille — Marseille

Identifiers

NCT: NCT07208929 · 2025-A00864-45

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗