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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age10-18
SponsorAssistance Publique Hopitaux De Marseille

About this trial

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

Eligibility criteria

Qualifiers

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)

Disqualifiers

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

Trial design

Treatments tested in this trial

  • MRI

Treatment groups

60 Participants
are divided into 2 treatment groups