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Validation of a New Generation of Optimized Orthoses for Personalized Treatment of Adolescent Idiopathic Scoliosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02285621
Enrollment
90
Registered
2014-11-07
Start date
2013-09-30
Completion date
2021-09-30
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adolescent Idiopathic Scoliosis (AIS), Scoliosis

Keywords

Scoliosis, Spine deformity, Brace, 3D

Brief summary

Adolescent Idiopathic scoliosis affects 3-4% of the Canadian population, of which about 10% will need a brace treatment during pubertal growth spurt. The design is made relatively corsets empirically, hence the relative efficiency of this treatment. Our team has developed innovative methods for design, optimization and computer aided manufacturing-based numerical simulation models customized to each patient, and a system of evaluation and adjustment of corsets. In this project, the investigators will evaluate the effectiveness of this platform customized treatment and demonstrate its clinical application

Interventions

OTHEROptimized brace versus conventional Boston brace

Surface topography using Inspeck cameras allows production of a 3D reconstruction of the patient's trunk, this reconstruction will help to produce the optimized brace. Radiographic and patient-reported data will be gathered and analyzed to observe changes between time points. All radiographs will be taken with an EOS imaging system to allow 3D reconstructions. The SRS-22r will be collected at all clinical visits. Study questions will be aligned as much as possible with other prospective scoliosis protocols so as to minimize patient and surgeon response burden. The study protocol requires no additional visits or radiographs beyond standard of care. Ibuttons are installed in each brace and used to measure the compliance of the patient.

Sponsors

St. Justine's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
10 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* 10 years or older * AIS diagnosis * Risser 0-2 * Primary curve angles 20 degrees - 40 degrees * If female, either premenarchal or less than 18 months postmenarchal.

Exclusion criteria

* Patients with a pre-existing cardiovascular condition * Patients with symptom of a neurological disorder * Patients with any other disorder of the musculoskeletal system affecting the lower limbs,

Design outcomes

Primary

MeasureTime frameDescription
Change in Cobb angleBaseline, 6 months, 1 yearRadiographics will be gathered and analyzed to observe changes between time points. All radiographs will be taken with an low-dose biplane radiographic system (EOS) to allow 3D reconstructions.

Secondary

MeasureTime frameDescription
Change in Scoliosis Research Society questionnaire (SRS-22r) scoresBaseline, 6 months, 1 yearThe SRS-22r questionnaire is available from SRS.org. It is a self-reported tools assessing self-image, function, pain, mental health with 5 questions each and satisfaction with care with 2 questions. A total score is also available based on all 22 questions.
Change in surface topographyBaseline, 6 months, 1 yearFour optical scanners are used to capture full trunk images. Subjects are positioned in a standard frame, and reference points marked. Parameters quantifying the external back surface deformity are assessed.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026