Validation of a New Generation of Optimized Orthoses for Personalized Treatment of Adolescent Idiopathic Scoliosis
Primary Purpose
Scoliosis, Adolescent Idiopathic Scoliosis (AIS)
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Optimized brace versus conventional Boston brace
Sponsored by
About this trial
This is an interventional treatment trial for Scoliosis focused on measuring Scoliosis, Spine deformity, Brace, 3D
Eligibility Criteria
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,
Sites / Locations
- CHU Sainte-Justine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Optimized brace
Standard brace
Arm Description
Test group: Patient will receive optimized brace (3D computer assisted design of the brace)
Control goup: Patient will receive the Boston Thoracolumbosacral orthosis (TLSO) (conventional design method)
Outcomes
Primary Outcome Measures
Change in Cobb angle
Radiographics 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 Outcome Measures
Change in Scoliosis Research Society questionnaire (SRS-22r) scores
The 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 topography
Four 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.
Full Information
NCT ID
NCT02285621
First Posted
September 5, 2014
Last Updated
November 23, 2021
Sponsor
St. Justine's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02285621
Brief Title
Validation of a New Generation of Optimized Orthoses for Personalized Treatment of Adolescent Idiopathic Scoliosis
Study Type
Interventional
2. Study Status
Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
September 2013 (Actual)
Primary Completion Date
September 2019 (Actual)
Study Completion Date
September 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Justine's Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Scoliosis, Adolescent Idiopathic Scoliosis (AIS)
Keywords
Scoliosis, Spine deformity, Brace, 3D
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Optimized brace
Arm Type
Experimental
Arm Description
Test group: Patient will receive optimized brace (3D computer assisted design of the brace)
Arm Title
Standard brace
Arm Type
Active Comparator
Arm Description
Control goup: Patient will receive the Boston Thoracolumbosacral orthosis (TLSO) (conventional design method)
Intervention Type
Other
Intervention Name(s)
Optimized brace versus conventional Boston brace
Intervention Description
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.
Primary Outcome Measure Information:
Title
Change in Cobb angle
Description
Radiographics 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.
Time Frame
Baseline, 6 months, 1 year
Secondary Outcome Measure Information:
Title
Change in Scoliosis Research Society questionnaire (SRS-22r) scores
Description
The 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.
Time Frame
Baseline, 6 months, 1 year
Title
Change in surface topography
Description
Four 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.
Time Frame
Baseline, 6 months, 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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,
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hubert Labelle, MD
Organizational Affiliation
St. Justine's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Sainte-Justine
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3T 1C5
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
28770254
Citation
Cobetto N, Aubin CE, Parent S, Barchi S, Turgeon I, Labelle H. 3D correction of AIS in braces designed using CAD/CAM and FEM: a randomized controlled trial. Scoliosis Spinal Disord. 2017 Jul 23;12:24. doi: 10.1186/s13013-017-0128-9. eCollection 2017.
Results Reference
derived
PubMed Identifier
26861663
Citation
Cobetto N, Aubin CE, Parent S, Clin J, Barchi S, Turgeon I, Labelle H. Effectiveness of braces designed using computer-aided design and manufacturing (CAD/CAM) and finite element simulation compared to CAD/CAM only for the conservative treatment of adolescent idiopathic scoliosis: a prospective randomized controlled trial. Eur Spine J. 2016 Oct;25(10):3056-3064. doi: 10.1007/s00586-016-4434-3. Epub 2016 Feb 9.
Results Reference
derived
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Validation of a New Generation of Optimized Orthoses for Personalized Treatment of Adolescent Idiopathic Scoliosis
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