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Trials of Intelligent Nighttime Brace With Smart Padding to Treat of Adolescent Idiopathic Scoliosis

Primary Purpose

Adolescent Idiopathic Scoliosis

Status
Enrolling by invitation
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Intelligent Nighttime 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, Bracing Treatment

Eligibility Criteria

10 Years - 13 Years (Child)FemaleDoes not accept healthy volunteers

Inclusion Criteria: between the ages of 10-13, scoliosis with a Cobb angle larger between 10 -25 degrees; No prior treatment Pre-menarche or post- menarche by no more than 1 year Ability to read and understand English or Chinese Physical and mental ability to adhere to intelligent nighttime braces protocol Exclusion Criteria: History of previous surgical or orthotic treatment for AIS Diagnosis of other musculoskeletal or developmental illness that might be responsible for the spinal curvature Contraindications for pulmonary and/ or exercise tests Psychiatric disorders Recent trauma

Sites / Locations

  • The Hong Kong Polytechnic University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intelligent Nighttime Brace

Arm Description

The design of intelligent nighttime brace will incorporate different mechanism, such as a) compression and pulling forces through a customisable rigid brace, b) lumbar flexion by using a supporting air-belt, c) three-point pressure system is used to exert corrective forces by the intelligent paddings in the transverse direction, d) adjust the pressure of the brace padding through a pressure monitoring system in accordance with the sleeping posture of the users

Outcomes

Primary Outcome Measures

The Cobb angle measurements of intelligent nighttime brace
Measure lateral curvature of vertebra on spine x-ray AP view (unit: degree) will be measured by using EOS® low does x-ray.

Secondary Outcome Measures

Contour control
Use a 3D body scanner to measure the contour asymmetry. By using 3D scanning images, the contour asymmetry changes over a six-month period will be assessed.
Force measurements and monitoring
Measure the brace interface pressure by the Novel Pliance-xf-16 analyser. The bio-mechanics of the intelligent nighttime brace are assessed by the changes of the pressure distribution. A real-time intelligent system is use to monitor the pressure distribution.
Health-related quality of life (SRS-22)
Measure the quality of life by validated questionnaire, Euroqol (EQ-5D-5L). The five dimensions of the descriptive system are mobility, self-care, regular activities, pain/comfort, and anxiety/depression. The patients with higher values represent a worse outcome.

Full Information

First Posted
March 16, 2023
Last Updated
September 22, 2023
Sponsor
The Hong Kong Polytechnic University
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1. Study Identification

Unique Protocol Identification Number
NCT05790031
Brief Title
Trials of Intelligent Nighttime Brace With Smart Padding to Treat of Adolescent Idiopathic Scoliosis
Official Title
Development of Intelligent Nighttime Brace With Smart Padding to Treat of Adolescent Idiopathic Scoliosis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
September 1, 2023 (Actual)
Primary Completion Date
December 31, 2027 (Anticipated)
Study Completion Date
December 31, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hong Kong Polytechnic University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Adolescent idiopathic scoliosis (AIS) is a three-dimensional spinal deformity usually associated with intervertebral rotation that takes place during adolescence. Generally, bracing treatment is a common option for scoliosis patients. Non-surgical treatment for scoliosis patients is to offer a conservative solution to treat their condition and encourage a higher degree of compliance by avoiding interference with their daily life activities. Therefore, intelligent nighttime braces have been developed to solve this issue, which are intended to be worn for inhibiting the advancement of spinal deformity during sleeping hours. However, its efficacy is still controversial. Intelligent nighttime brace with a specialized design for teenagers with scoliosis is limited and most part of them are lack of mobility and lack of control over corrective forces on particular regions of the vertebra. A scientific approach should be used to design and develop intelligent nighttime brace as a treatment option for adolescents with early scoliosis.
Detailed Description
The design of intelligent nighttime brace with smart padding for adolescent idiopathic scoliosis will incorporate different mechanisms, such as compression and pulling forces through a customizable rigid brace lumbar flexion by using a supporting air-belt. three-point pressure system is used to exert corrective forces by the intelligent paddings in the transverse direction adjust the pressure of the brace padding through a pressure monitoring system in accordance with the sleeping posture of the users

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescent Idiopathic Scoliosis
Keywords
Scoliosis, Bracing Treatment

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Intelligent Nighttime Brace
Arm Type
Experimental
Arm Description
The design of intelligent nighttime brace will incorporate different mechanism, such as a) compression and pulling forces through a customisable rigid brace, b) lumbar flexion by using a supporting air-belt, c) three-point pressure system is used to exert corrective forces by the intelligent paddings in the transverse direction, d) adjust the pressure of the brace padding through a pressure monitoring system in accordance with the sleeping posture of the users
Intervention Type
Device
Intervention Name(s)
Intelligent Nighttime Brace
Intervention Description
Participants will be invited to undergo a fitting session of intelligent nighttime brace. After the fitting, participants will join a 6-month wear trial of the intelligent nighttime brace. Participants are required to wear the intelligent nighttime brace for 8 hours a day during sleeping and compliance will be recorded by an intelligent monitoring system. Participants will be invited to undergo assessments before the wear trial, after the trials of 3 months and after the trial of 6 months. The measure outcomes of the assessment include 1)ultrasound scanning image, 2)3D body scanning, 3)garment pressure, 4) questionnaires
Primary Outcome Measure Information:
Title
The Cobb angle measurements of intelligent nighttime brace
Description
Measure lateral curvature of vertebra on spine x-ray AP view (unit: degree) will be measured by using EOS® low does x-ray.
Time Frame
2 hours after wearing the brace and 6 months
Secondary Outcome Measure Information:
Title
Contour control
Description
Use a 3D body scanner to measure the contour asymmetry. By using 3D scanning images, the contour asymmetry changes over a six-month period will be assessed.
Time Frame
6 months
Title
Force measurements and monitoring
Description
Measure the brace interface pressure by the Novel Pliance-xf-16 analyser. The bio-mechanics of the intelligent nighttime brace are assessed by the changes of the pressure distribution. A real-time intelligent system is use to monitor the pressure distribution.
Time Frame
6 months
Title
Health-related quality of life (SRS-22)
Description
Measure the quality of life by validated questionnaire, Euroqol (EQ-5D-5L). The five dimensions of the descriptive system are mobility, self-care, regular activities, pain/comfort, and anxiety/depression. The patients with higher values represent a worse outcome.
Time Frame
6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: between the ages of 10-13, scoliosis with a Cobb angle larger between 10 -25 degrees; No prior treatment Pre-menarche or post- menarche by no more than 1 year Ability to read and understand English or Chinese Physical and mental ability to adhere to intelligent nighttime braces protocol Exclusion Criteria: History of previous surgical or orthotic treatment for AIS Diagnosis of other musculoskeletal or developmental illness that might be responsible for the spinal curvature Contraindications for pulmonary and/ or exercise tests Psychiatric disorders Recent trauma
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joanne Yip, phd
Organizational Affiliation
The Hong Kong Polytechnic University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Hong Kong Polytechnic University
City
Hong Kong
Country
China

12. IPD Sharing Statement

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Trials of Intelligent Nighttime Brace With Smart Padding to Treat of Adolescent Idiopathic Scoliosis

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