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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03332251
Other study ID # GRF2017
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date March 1, 2018
Est. completion date December 31, 2025

Study information

Verified date September 2023
Source The Hong Kong Polytechnic University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Adolescent idiopathic scoliosis (AIS) is a prevalent chronic condition that gradually leads to the three dimensional deformity of the spine. Spine curvature increases in youths as puberty progresses. Generally, only observation is suggested for adolescents with early scoliosis (Cobb's angle ≤ 20°). Rigid brace treatment is too draconian for them due to the high corrective force which nearly constrains all movements. Flexible brace treatment is an alternative option; however, its efficacy is still controversial. Posture correction girdle with a specialized design for teenagers with scoliosis is limited and most part of them can only provide some improvement for bad postures, such as hunchback. A scientific approach should be used to design and develop posture correction girdle as a treatment option for adolescents with early scoliosis.


Description:

The design of posture correction girdle will incorporate different mechanisms, such as 1. compression and pulling forces through a close fit of the intimate apparel 2. lumbar flexion by using a supporting belt 3. transverse forces applied by inserting pads inside the pocket lining by using the principle of the 3-point pressure system 4. axial rotation or coupled motion by using a system with uneven straps, and 5. an active mechanism that aims to shift the trunk away from areas of pressure.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 15
Est. completion date December 31, 2025
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender Female
Age group 10 Years to 13 Years
Eligibility Inclusion Criteria: - Diagnosis of AIS - Cobb's angle 10°-20° - Risser grade = 2 - 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 anisotropic textile braces protocol Exclusion Criteria: - 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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Posture Correction Girdle
Participants will be invited to undergo a fitting session of posture correction girdle. After the fitting, participants will join a 6-month wear trial of the posture correction girdle. Participants are required to wear the girdle for 8 hours a day and the compliance will be recorded by a logbook daily. Participants will be invited to undergo assessments before the wear trial, after the trial of 3 months, and after the trial of 6 months. The measure outcomes of the assessment include 1) ultrasound scanning image, 2) 3D body scan, 3) electromyography signal, 4) garment pressure, and 5) questionnaire.

Locations

Country Name City State
China The Hong Kong Polytechnic University Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
The Hong Kong Polytechnic University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effectiveness of posture correction girdle The spinal curve progression is said to be under control if the increase in the Cobb's angle is <5° 6 months
Secondary Posture improvement Improvement of posture by clinical photographs assessment 6 months
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