Safety and Efficacy of Posture Correction Girdle for Adolescent With Early Scoliosis

Sponsor
The Hong Kong Polytechnic University (Other)
Overall Status
Completed
CT.gov ID
NCT01776736
Collaborator
(none)
50
1
1
114
0.4

Study Details

Study Description

Brief Summary

For AIS, the caring of patients with spinal deformities has a long and varied history. Severe spinal deformities can greatly reduce pulmonary and cardiac functions, which may lead to death from cardiopulmonary failure. Therefore, surgery is generally suggested when the curvature of the spine is greater than 45-50 degrees. The adverse psychological impact of orthoses treatment on patients and its poor compliance has been a well-recognised problem. Some orthotic research studies indicate that early intervention of spinal deformities is particularly desirable. Taking into consideration current clinical practices, if the curve is less than 20 degrees, even if the child is at a high risk of progressive spinal deformity during the age of 10-16 at puberty, treatment is nothing more than just observation.

This project aims to combine clinical experience with textile and materials sciences to research and develop a posture correction girdle for adolescents with early scoliosis. As a result, this will reduce the future likelihood of brace wear or surgery.

In this study, the eligible subjects will be given tailor-made posture correction girdles to wear it 8 hours daily. Monitoring and observation will be provided during the six months girdling period. Data will be collected before and after the girdling by X-ray radiograph for analysis, in order to comparison the spine curvature condition. Locomotion of the subject with and without wearing the posture correction girdle will also be reference.

Condition or Disease Intervention/Treatment Phase
  • Device: Posture Correction Girdle
N/A

Detailed Description

For AIS, the caring of patients with spinal deformities has a long and varied history. Severe spinal deformities can greatly reduce pulmonary and cardiac functions, which may lead to death from cardiopulmonary failure. Therefore, surgery is generally suggested when the curvature of the spine is greater than 45-50 degrees. The adverse psychological impact of orthoses treatment on patients and its poor compliance has been a well-recognised problem. Some orthotic research studies indicate that early intervention of spinal deformities is particularly desirable. Taking into consideration current clinical practices, if the curve is less than 20 degrees, even if the child is at a high risk of progressive spinal deformity during the age of 10-16 at puberty, treatment is nothing more than just observation.

This project aims to combine clinical experience with textile and materials sciences to research and develop a posture correction girdle for adolescents with early scoliosis. As a result, this will reduce the future likelihood of brace wear or surgery.

The eligible subjects will be given tailor-made posture correction girdles. Monitoring and observation will be provided during the girdling period. Data will be collected before and after the girdling by X-ray radiograph for analysis, in order to comparison the spine curvature condition. Locomotion of the subject with and without wearing the posture correction girdle will also be reference.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Study of Posture Correction Girdle of Adolescents With Early Scoliosis
Actual Study Start Date :
Jul 1, 2012
Actual Primary Completion Date :
Dec 30, 2020
Actual Study Completion Date :
Dec 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Posture Correction Girdle

Posture Correction Girdle applied for 8 hours per day. Clinical, radiographic, and self-report follow-up within the girdling period (6 months).

Device: Posture Correction Girdle
Posture Correction Girdle applied for 8 hours per day. Clinical, radiographic, and self-report follow-up within the girdling period (6 months).

Outcome Measures

Primary Outcome Measures

  1. Progression of the spinal curve [From baseline to 6 months]

    No progression of the spinal curve (no increase of Cobb angle) by radiographic measures.

Secondary Outcome Measures

  1. Progression of the spinal curve [From baseline to 6 months]

    The progression of the spinal curve within control (increase of Cobb angle < 5 degrees)

  2. Posture improvement [From baseline to 6 months]

    Improvement of posture by clinical photographs assessment

Eligibility Criteria

Criteria

Ages Eligible for Study:
10 Years to 13 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Aged 10 to 13 years

  • Diagnosis of AIS in early stage

  • Primary Cobb angle equals to or less than 20 degrees

  • Pre-menarchal or post-menarchal by no more than 1 year

  • Ability to read and understand English or Chinese

  • At high risk for curve progression

  • Skeletally immature (Risser grade 0, 1, or 2)

  • Physical and mental ability to adhere to posture correction girdle protocol

Exclusion Criteria:
  • Contraindications for x-ray exposure

  • Diagnosis of other musculoskeletal or developmental illness that might be responsible for the spinal curvature

  • History of previous surgical or orthotic treatment for AIS

  • Contraindications for pulmonary and / or exercise tests

  • Psychiatric disorders

  • Recent trauma

  • Recent traumatic (emotional) event

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Hong Kong Polytechnic University Hong Kong China

Sponsors and Collaborators

  • The Hong Kong Polytechnic University

Investigators

  • Principal Investigator: Joanne Yip, PhD, The Hong Kong Polytechnic University
  • Study Chair: Kit-Lun Yick, Ph.D, The Hong Kong Polytechnic University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Joanne Yip, Lecturer, The Hong Kong Polytechnic University
ClinicalTrials.gov Identifier:
NCT01776736
Other Study ID Numbers:
  • ITF-237-11
First Posted:
Jan 28, 2013
Last Update Posted:
Aug 16, 2022
Last Verified:
Aug 1, 2022
Keywords provided by Joanne Yip, Lecturer, The Hong Kong Polytechnic University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 16, 2022