AzTrials
AzTrials

Adolescent Idiopathic ScoliosisNCT04117334

Determining Best Indications for Bracing for Adolescent Idiopathic Scoliosis

An observational study of Adolescent Idiopathic Scoliosis, run by The University of Hong Kong at 2 sites in Hong Kong.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

This is a prospective study for Investigating the cost-effectiveness of current bracing protocols for adolescent idiopathic scoliosis (AIS). It is hypothesized that aggressive management of adolescent idiopathic scoliosis (AIS) including early bracing at mild curve magnitudes and surgery at 40 degrees is more… Read more about this study

Who is it for?
Ages 10 to 18 years
Conditions the study is for
Adolescent Idiopathic Scoliosis
What is being tested?
Bracing
How many people
700 participants
Where
2 sitesHong Kong
Study dates
1 Dec 2016to 31 Mar 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 10 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Study population: This is a prospective cohort of AIS patients who are newly prescribed with bracing treatment

Who may be able to join

  • Patients who are diagnosed with adolescent idiopathic scoliosis and are seen in the first setting with remaining growth potential (Risser 0-2), and are prescribed with either underarm (Boston) or Milwaukee bracing

Who cannot join

  • Patients whose diagnosis is not adolescent idiopathic scoliosis, unable to comply with study follow-up and refused consent for study

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Jason Cheung, MBBS, MS contact

(852)22554581 ext. 85222554581

cheungjp@hku.hk

Hong Kong2 sites, 2 recruiting
  • Duchess of Kent Children's Hospital

    Hong Kong

    Jason Cheung, 85222554581 ext. 85222554581, cheungjp@hku.hk

    Recruiting
  • Jason Pui Yin Cheung

    Hong Kong

    Jason Pui Yin Cheung, 22554581, cheungjp@hku.hk

    Recruiting

Other trials in Hong Kong

About this study

Official title: Determining the Best Indications for Initiating Brace Treatment for Adolescent Idiopathic Scoliosis

This is a prospective study for Investigating the cost-effectiveness of current bracing protocols for adolescent idiopathic scoliosis (AIS). It is hypothesized that aggressive management of adolescent idiopathic scoliosis (AIS) including early bracing at mild curve magnitudes and surgery at 40 degrees is more cost-effective while maintaining similar health quality of life. Scoliosis Research Society 22-item and EuroQol- 5 dimension questionnaires and direct/indirect medical costs will be utilized for the cost-effectiveness analysis and health related quality of life assessment. The findings of this study have the potential to improve decision-making and revolutionize care of AIS patients in Hong Kong and globally. Clinicians will be able to utilize our results to provide the best and most cost-effective timing for initiating brace treatment.

Read the detailed description

Bracing is the mainstay treatment for preventing adolescent idiopathic scoliosis (AIS) progression and the main purpose for treatment is to prevent deformities from reaching the surgical threshold. It has been shown to be effective at reducing curve progression especially in patients with good compliance to treatment. However, bracing should not be used indiscriminately as certain complications have been reported. Bracing too early is safe for curve control but may subject children to prolonged discomfort with the bracing and increased consumption of resources for periodic brace fabrication. Prolonged bracing also reduces spinal mobility, lead to poor body image and self-esteem, and worsen quality of life. Additional risks of osteoporosis and muscular atrophy may also occur. Hence, being able to initiate prompt and appropriate bracing is crucial for achieving optimal curve control and avoiding complications.

Yet, there are still have difficulties identifying patients who may deteriorate. Generally speaking, skeletally immature AIS patients with curves of 20-40 degrees should consider bracing. However, not all of these patients require bracing and some may not need any treatment. More importantly, the resulting curve magnitude on radiographs may not correlate directly with health-related quality of life (HRQOL) measures. As such, the relationship of the Cobb angle prior to initiating brace treatment with long-term HRQOL measures is unknown. The above suggest that there is a significant gap in our knowledge of the optimal timing of brace initiation for managing AIS patients.

In the current setting of rising health-care expenditures, it is also important to assess the "value" of management options and provide the best and cost-effective care for our AIS patients without compromising outcomes or safety. Some clinicians may be more aggressive by bracing children with minor curves while some are content with prescribing braces only when deterioration occurs in moderate curves. In this modern era of healthcare, there is increasing emphasis placed on monitoring and controlling health-care costs to the patient, hospital and insurance companies. Hence, it is an appropriate time to consider the relationship of cost-effectiveness factors and HRQOL measures in designing bracing protocols for AIS patients. With increasing health-care costs, consumption of resources, and the imperative to provide the best healthcare to these children, and focus on a cost-effective delivery of care.

It is thus timely for us to perform this prospective cost-effectiveness comparative study to identify the best indications for initiating brace treatment for AIS patients. Evidence for the best HRQOL outcomes at the lowest cost from both the patient and health-care perspective is necessary to further improve the care for AIS patients. There is potential for the derived model to be applied in other healthcare systems by using a more personalized approach.

For this study, the investigators will utilize mathematical modeling based on factors including initial Cobb angle, maturity status, brace duration, and HRQOL measures to determine the best cost-effective indications for brace treatment. Outcomes will be dependent on the Cobb angle at the end of bracing, HRQOL measures and the overall costs incurred to patients and infrastructure. Our hypothesis is given an AIS patient with significant growth potential, a Cobb angle of 25 degrees is most cost-effective for initiating bracing. On the contrary, bracing for subjects with Cobb angles of 40 degrees or more is not cost-effective regardless of remaining growth.

The main objectives of this study are:

  1. To assess the cost-effectiveness of current bracing protocols for AIS.
  2. To create a mathematical model that will determine the most cost-effective threshold for initiating brace treatment based on health quality of life measures.

This is a prospective comparative cost-effectiveness analysis between bracing groups. This study will be carried out at the Duchess of Kent Children's Hospital (DKCH). Prospective collection of data from AIS patients including clinical and radiographic information. The investigators will only include AIS patients seen in the first setting with remaining growth potential (Risser 0-2) that may be considered for bracing, and will be prescribed with either underarm (Boston) or Milwaukee bracing. The investigators will collect a minimum of two-year longitudinal data, having at least 5 follow-up data points or clinic visits. It is clinic protocol that all subjects undergo weight, height and arm span measurements, radiographs and doctor assessments at these visits. For this study, HRQOL and utility measurements are vital to its success. Thus, the SRS-22r and EQ-5D-5L questionnaire will be provided at every visit. Three subgroups for analysis between groups. For groups of baseline Cobb angles (20-<35, 35-40, >40 degrees)

Direct and indirect cost will be analyzed. The medical cost (direct costs) for each patient since the first presentation will be obtained. The cost includes the expenses for clinic follow-up, any form of outpatient and inpatient treatment (including physiotherapy, scoliosis specific exercises, bracing) and complications. Unit cost of investigation, treatment and follow-up will be based on the Hospital Authority official charges to non-eligible persons available in the 2013 Hong Kong Government Gazette and updated charges in Hospital Authority website. Brace costs include the number of orthotic visits, per visit consultation cost for the orthotist fabrication of the brace, consumables for use, number of exchanges or modifications, and the thermal sensor for monitoring compliance. In addition to the orthotist, other allied health professionals are also part of the bracing program which further increases the cost. Physiotherapists are involved to maintain body posture and teach/perform scoliosis specific exercises. A clinical psychologist will periodically assess the patient and family to maintain mental health. will be included in the cost analysis. For subjects with failed conservative treatment meaning progression of the curve and no longer indicated for bracing or further bracing will undergo surgical intervention. These subjects are still analyzed but an addition cost item of "surgery" (one lump-sum to cover general cost of implants, hospital length of stay, operating theater cost) will be included. The cost of family members missing work (indirect costs) will also be assessed.

Cost-effectiveness analysis of initiating for bracing will be performed via Markov modelling that will simulate the clinical management of AIS patients since first presentation assuming at age of 11 years (female). Each patient starting at the assumed age 11 will thus follow an annual cycle with a time horizon until 18 years of age. Modelling will be carried out for the AIS patients as a whole, and by the 5 Cobb angle magnitude groups (20-25 degrees, >25-30 degrees, >30-35 degrees, >35-40 degrees, and >40 degrees). For each cycle year, patients initiating bracing may wear the brace until maturity, stop wearing (compliance rate), or switch to surgical approach over the years. Patients with failed bracing will proceed to surgery, and stay with a post-operation health status from operation date to the end. Costs and utility data for AIS patients initiating bracing will be obtained from above prospective study. Clinical model parameters related to compliance rate of bracing, maturity rate of bracing, probability of treatment switch from bracing to surgery will also be identified through a comprehensive review of local and overseas literature as reference. Based on the regression model found, the investigators will estimate the effects of bracing at variable initial curvature and maturity status on direct and indirect costs, SRS-22r domain and total scores, and EQ-5D utility scores. The cost-effectiveness analysis will also recommend a threshold of curvature and maturity combination to indicate when bracing initiated will be the most cost-effective or even cost-saving treatment option for AIS patients.

Being tested
Bracing
Keywords
Bracing, Cost-effectiveness, Adolescent idiopathic scoliosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BracingOther

Study groups in NCT04117334
Study groupRoleWhat they receive
Bracing AIS patientsThese are patients undergoing brace treatment for AIS
Receives: Other: Bracing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Cobb angle

    Cobb angle changes from final visit as compared to baseline

    Measured: up to 3 years

  2. Cost-effectiveness of bracing - direct and indirect costs

    Costs involve number of clinic follow-up, any form of outpatient and inpatient treatment (including physiotherapy, scoliosis specific exercises, bracing) and complications. Unit cost of investigation, treatment and follow-up. These will be analyzed against the benefits of bracing on clinical parameters, that is, any deterioration of Cobb angle

    Measured: up to 3 years

  3. Change in C7-CSVL

    Changes in C7-central sacral vertical line with brace follow-up

    Measured: up to 3 years

  4. Change in truncal shift

    Changes in truncal shift with brace follow-up

    Measured: up to 3 years

  5. Change in sagittal vertical axis

    Change sagittal vertical axis with brace follow-up

    Measured: up to 3 years

  6. Change in thoracic kyphosis

    Change in thoracic kyphosis with brace follow-up

    Measured: up to 3 years

  7. Change in lumbar lordosis

    Change in lumbar lordosis with brace follow-up

    Measured: up to 3 years

  8. Change in rotational profile

    Change in 3D parameters/apical rotation with brace follow-up

    Measured: up to 3 years

Secondary outcomes (3)
  1. Patient's quality of life - SRS-22r

    Using the refined Chinese version of the Scoliosis Research Society-22 (SRS-22r) questionnaire scores changes of total score and domain scores (Domains: Activity, Self-image, Pain, Mental Health, Satisfaction with Treatment). The highest score is 5 for total score and each domain score. The higher the score, the better the patient's quality of life is.

    Total

    Measured: up to 3 years

  2. Patient's quality of life - EQ5DY

    Using the changes of EQ5DY scores (total score and dimension scores: Mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, and EQ-visual analogue scale (EQ-VAS)). Each dimension has 5 levels of response and each response will provide one digit to represent it. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state. These health states can be converted into a single index value by using the standard EQ-value sets for the local population. For the EQ-VAS, it is a patient's perception of own general health status on a scale from 0 to 100, with higher the score, the better the status.

    Measured: up to 3 years

  3. Brace compliance

    Thermal sensor objective compliance data

    Measured: up to 3 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Oct 2019
  2. Study start1 Dec 2016
  3. Primary completion31 Dec 2025 (estimated)
  4. Study completion31 Mar 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
700 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04117334
Sponsor's protocol ID
PB version 1.0
Status last verified
Nov 2024
First submitted
30 Sep 2019
Last updated
6 Dec 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Adolescent Idiopathic Scoliosis, run by The University of Hong Kong at 2 sites in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Jason Cheung, MBBS, MS ((852)22554581 ext. 85222554581, cheungjp@hku.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Cobb angle (time frame: up to 3 years). The study lists 8 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Dec 2024.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in