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Ergonomic Brace Wear for Adolescent Idiopathic Scoliosis

Primary Purpose

Adolescent Idiopathic Scoliosis

Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Ergonomic Brace vs hard brace
Sponsored by
The Hong Kong Polytechnic University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adolescent Idiopathic Scoliosis focused on measuring Scoliosis brace, Conventional treatment for Adolescent Idiopathic Scoliosis, In-brace correction, Trunk listing, Vertebral rotation, Interface pressure, 3D body scanning, Surface topography, Trunk asymmetry, Quality of Life

Eligibility Criteria

10 Years - 14 Years (Child)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 10 or older when brace is prescribed
  • Risser 0 to 2
  • Primary curve angles 25° to 40°
  • Female, who were either pre-menarche or less than 1 year of post-menarche
  • Undergoing hard brace treatment

Exclusion Criteria:

  • Low risk of curve progression
  • Non-idiopathic scoliosis (e.g. congenital, neuromuscular deformities)

Sites / Locations

  • The Hong Kong Polytechnic University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Ergonomic Brace vs hard brace

Arm Description

Ergonomic Brace is a new design of scoliosis brace, which consists of a knit bodice as base and also resin bones, paddings, straps and a pelvic belt as auxiliaries for spinal correction. The purpose of the bones is to keep the posture of patient upright. Paddings are placed at the convex regions of the spine while straps are used to input directional force onto the paddings. Pelvic belt, on the other hand, is for stabilizing the pelvis in order to achieve an effective spinal correction. The biomechanical principles for the correction of spine has considered both the frontal and sagittal planes, where the overall brace mechanism follows the Rigo classification. Hard brace is the brace which the participants are currently using for their ongoing conservative treatment.

Outcomes

Primary Outcome Measures

Immediate in-brace correction of spinal curve
Cobb angle: more than/equal to 40% correction (lumbar/thoracolumbar curve); slightly less than/close to 40% correction (thoracic curve)

Secondary Outcome Measures

Immediate in-brace correction of vertebral rotation assessed by the Global Torsion Index
Global torsion index: to quantify detorsion by averaging the 17 segmental rotations of thoracic and lumbar vertebrae Higher index score = the average segmental rotations of the 17 vertebrae is higher; Lower index score = the average segmental rotations of the 17 vertebrae is lower The global torsion index which result from wearing the Ergonomic Brace will be compared with which of hard brace. A higher/similar detorsion percentage as hard brace is considered satisfactory.
Immediate in-brace correction of trunk listing assessed by the plumb line method
Plumb line method: to assess the coronal and sagittal balance by drawing a vertical line from the mid-point of the C7 vertebra down to the sacrum Positive balance: the plumb line passes more than 2 cm in front of the posterosuperior corner of the S1 vertebral body Neutral balance: the plumb line passes within 2 cm of the posterosuperior corner of the S1 vertebral body Negative balance: the plumb line passes more than 2 cm behind the posterosuperior corner of the S1 vertebral body Measurement of trunk listing is significant in the treatment of scoliosis curve, as it is related to the trunk aesthetic profile of the subjects, and besides, sagittal balance of the spine and pelvis is correlated with the progression of scoliosis. An improvement in the coronal and sagittal balance of spine resulting from wearing the Ergonomic Brace is therefore considered satisfactory.
Improvement in trunk asymmetry assessed by the POTSI index
Posterior Trunk Symmetry Index (POTSI): to compare the surface topography change before and after wearing the Ergonomic Brace POTSI index: a parameter used for assessing the trunk asymmetry and deformity in the coronal plane All measurements will be performed on the 3D surface topography scans. Ideal value of POTSI is zero, meaning full asymmetry of the posterior and anterior trunk respectively. Normal value of POTSI should lie below 27. The performance of the Ergonomic Brace in terms of improving the trunk asymmetry of participants is considered effective when the index is scored within normal value (i.e. 0-27).
Improvement in trunk asymmetry assessed by the ATSI index
Anterior Trunk Symmetry Index (ASTI): to compare the surface topography change before and after wearing the Ergonomic Brace ATSI index: a parameter used for assessing the trunk asymmetry and deformity in the frontal plane All measurements will be performed on the 3D surface topography scans. Ideal value of ATSI is zero, meaning full asymmetry of the posterior and anterior trunk respectively. Normal value, on the other hand, should lie below 27 for each index. The performance of the Ergonomic Brace in terms of improving the trunk asymmetry of participants is considered effective when the index is scored within normal value (i.e. 0-27).

Full Information

First Posted
July 25, 2018
Last Updated
February 11, 2020
Sponsor
The Hong Kong Polytechnic University
Collaborators
Innovation and Technology Commission, Hong Kong, The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT03617120
Brief Title
Ergonomic Brace Wear for Adolescent Idiopathic Scoliosis
Official Title
Ergonomic Brace Wear for Adolescent Idiopathic Scoliosis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
December 31, 2019 (Actual)
Study Completion Date
January 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hong Kong Polytechnic University
Collaborators
Innovation and Technology Commission, Hong Kong, The University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
This study assesses the effectiveness of a new scoliosis brace design for adolescent idiopathic scoliosis (AIS) patients, named Ergonomic Brace, by comparing the outcome with hard brace in terms of three aspects: To assess the efficacy in spinal correction To evaluate the improvement made to the body appearance of AIS subjects To evaluate the impacts on the quality of life (QoL) of AIS subjects All participants will be fitted with an Ergonomic Brace and required to wear it during the days of experiment only. The ongoing treatment with hard brace will not be substituted with the Ergonomic Brace, unless its immediate treatment effect is equivalent to hard brace and with approval from the doctor.
Detailed Description
To assess the efficacy in spinal correction The efficacy of the Ergonomic Brace refers to the magnitude of spinal correction that could be obtained for patients with AIS. The assessments in this study focus on two aspects, which are i) the in-brace correction and ii) the interface pressure. In-brace correction is used to judge the quality of bracing and also a prognostic indicator for the long-term treatment outcome. Clinical parameters such as Cobb angle, vertebral rotation and trunk listing will be measured with radiographs by a single observer. Interface pressure in this study refers to the pressure between the brace and the trunk of subject. The purpose is to assess the time response of trunk to the intervention of the Ergonomic Brace, and correlation will also be made with the extent of spinal correction. To evaluate the improvement made to the body appearance of AIS subjects The trunk aesthetic profile of AIS subjects are being affected by spinal deformities. Surface topography of the subjects will be captured by 3D body scanner, and followed by the evaluation of body aesthetics through the trunk asymmetry scales called POTSI and ATSI index. The purpose is to compare the surface topography change before and after wearing the Ergonomic Brace. To evaluate the impacts on the QoL of AIS subjects Bracing can negatively affect the QoL of patients with AIS. The Chinese version of Brace Questionnaire (BrQ) will be adopted in this study to compare the impact of hard brace and Ergonomic Brace on the QoL of AIS subjects. Difficulties experienced by AIS subjects during bracing will be highlighted and used for future improvements in scoliosis brace design.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescent Idiopathic Scoliosis
Keywords
Scoliosis brace, Conventional treatment for Adolescent Idiopathic Scoliosis, In-brace correction, Trunk listing, Vertebral rotation, Interface pressure, 3D body scanning, Surface topography, Trunk asymmetry, Quality of Life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ergonomic Brace vs hard brace
Arm Type
Experimental
Arm Description
Ergonomic Brace is a new design of scoliosis brace, which consists of a knit bodice as base and also resin bones, paddings, straps and a pelvic belt as auxiliaries for spinal correction. The purpose of the bones is to keep the posture of patient upright. Paddings are placed at the convex regions of the spine while straps are used to input directional force onto the paddings. Pelvic belt, on the other hand, is for stabilizing the pelvis in order to achieve an effective spinal correction. The biomechanical principles for the correction of spine has considered both the frontal and sagittal planes, where the overall brace mechanism follows the Rigo classification. Hard brace is the brace which the participants are currently using for their ongoing conservative treatment.
Intervention Type
Device
Intervention Name(s)
Ergonomic Brace vs hard brace
Intervention Description
Visit 1: Usual check-up: standing in-brace radiograph of hard brace and doctor consultation Pressure measurement of participant wearing their hard brace Visit 2: Brace Questionnaire (BrQ) for hard brace; Trunk Appearance Perception Scale (TAPS) 3D body scanning (before wearing the Ergonomic Brace) Fitting of the Ergonomic Brace Pressure measurement of participant wearing the Ergonomic Brace (instant) Pressure measurement of participant wearing the Ergonomic Brace (after 2 hours) 3D body scanning (after wearing the Ergonomic Brace for 2 hours) Brace Questionnaire (BrQ) for the Ergonomic Brace Visit 3: Standing in-brace radiograph of the Ergonomic Brace Doctor consultation
Primary Outcome Measure Information:
Title
Immediate in-brace correction of spinal curve
Description
Cobb angle: more than/equal to 40% correction (lumbar/thoracolumbar curve); slightly less than/close to 40% correction (thoracic curve)
Time Frame
2 hours
Secondary Outcome Measure Information:
Title
Immediate in-brace correction of vertebral rotation assessed by the Global Torsion Index
Description
Global torsion index: to quantify detorsion by averaging the 17 segmental rotations of thoracic and lumbar vertebrae Higher index score = the average segmental rotations of the 17 vertebrae is higher; Lower index score = the average segmental rotations of the 17 vertebrae is lower The global torsion index which result from wearing the Ergonomic Brace will be compared with which of hard brace. A higher/similar detorsion percentage as hard brace is considered satisfactory.
Time Frame
2 hours
Title
Immediate in-brace correction of trunk listing assessed by the plumb line method
Description
Plumb line method: to assess the coronal and sagittal balance by drawing a vertical line from the mid-point of the C7 vertebra down to the sacrum Positive balance: the plumb line passes more than 2 cm in front of the posterosuperior corner of the S1 vertebral body Neutral balance: the plumb line passes within 2 cm of the posterosuperior corner of the S1 vertebral body Negative balance: the plumb line passes more than 2 cm behind the posterosuperior corner of the S1 vertebral body Measurement of trunk listing is significant in the treatment of scoliosis curve, as it is related to the trunk aesthetic profile of the subjects, and besides, sagittal balance of the spine and pelvis is correlated with the progression of scoliosis. An improvement in the coronal and sagittal balance of spine resulting from wearing the Ergonomic Brace is therefore considered satisfactory.
Time Frame
2 hours
Title
Improvement in trunk asymmetry assessed by the POTSI index
Description
Posterior Trunk Symmetry Index (POTSI): to compare the surface topography change before and after wearing the Ergonomic Brace POTSI index: a parameter used for assessing the trunk asymmetry and deformity in the coronal plane All measurements will be performed on the 3D surface topography scans. Ideal value of POTSI is zero, meaning full asymmetry of the posterior and anterior trunk respectively. Normal value of POTSI should lie below 27. The performance of the Ergonomic Brace in terms of improving the trunk asymmetry of participants is considered effective when the index is scored within normal value (i.e. 0-27).
Time Frame
0 and 6 month
Title
Improvement in trunk asymmetry assessed by the ATSI index
Description
Anterior Trunk Symmetry Index (ASTI): to compare the surface topography change before and after wearing the Ergonomic Brace ATSI index: a parameter used for assessing the trunk asymmetry and deformity in the frontal plane All measurements will be performed on the 3D surface topography scans. Ideal value of ATSI is zero, meaning full asymmetry of the posterior and anterior trunk respectively. Normal value, on the other hand, should lie below 27 for each index. The performance of the Ergonomic Brace in terms of improving the trunk asymmetry of participants is considered effective when the index is scored within normal value (i.e. 0-27).
Time Frame
0 and 6 month

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 10 or older when brace is prescribed Risser 0 to 2 Primary curve angles 25° to 40° Female, who were either pre-menarche or less than 1 year of post-menarche Undergoing hard brace treatment Exclusion Criteria: Low risk of curve progression Non-idiopathic scoliosis (e.g. congenital, neuromuscular deformities)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joanne Yip
Organizational Affiliation
The Hong Kong Polytechnic University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Hong Kong Polytechnic University
City
Tsim Sha Tsui
State/Province
Kolwoon
ZIP/Postal Code
00852
Country
Hong Kong

12. IPD Sharing Statement

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Ergonomic Brace Wear for Adolescent Idiopathic Scoliosis

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