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Trial on Three Treatments for Scoliosis (CONTRAIS)

Primary Purpose

Idiopathic Scoliosis

Status
Active
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Hypercorrective night-time brace
Scoliosis specific exercises.
Self-mediated physical activity.
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Scoliosis focused on measuring Idiopathic scoliosis, Brace, Scoliosis specific exercise, Physical activity

Eligibility Criteria

9 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of idiopathic scoliosis
  • Skeletally immature with estimated remaining growth for at least one year.
  • Not more than one year after menarche
  • Primary Cobb angle between 25 and 40 degrees.
  • Curve apex T7 or caudal

Exclusion Criteria:

  • Scoliosis with a possible non-idiopathic ethiology. Patients will be excluded from the study if the pathogenesis of the scoliosis is not idiopathic, but due to a neuromuscular, neurological, congenital malformation or trauma related comorbidity.
  • Previous brace or surgical treatment for scoliosis.

Sites / Locations

  • Mälarsjukhuset / Eskilstuna hospital
  • Ryhov Hospital
  • Linköping University, Linköping University Hospital
  • Karolinska University Hospital
  • Sundsvall Hospital
  • Umeå University, Norrland University Hospital
  • Västerås Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Brace

Scoliosis specific exercises.

Self-mediated physical activity.

Arm Description

Hypercorrective night-time brace worn 8 hours per night. A prescription of general physical activity will be provided at a dose of 60 minutes per day. Instructions regarding physical activity will be delivered during a one hour session.

Scoliosis specific exercises. The intervention will be delivered in 3 x 90 minute sessions, once per month during the first 3 months. An additional session will be provided every 6 months for the entirety of the study. A prescription of general physical activity will be provided at a dose of 60 minutes per day.

A prescription of general physical activity will be provided at a dose of 60 minutes per day. Instructions will be delivered during a 1 hour session.

Outcomes

Primary Outcome Measures

Radiological progression of scoliosis
Progression of the Cobb angle more than 6 degrees, compared to the primary x-ray, seen on two consecutive spinal standing x-rays.

Secondary Outcome Measures

Quality of life assessed with questionnaire instruments
Quality of life measured with validated questionnaires such as Euroqol (EQ5D-Y), Scoliosis Research Society outcomes questionnaire 22r (SRS22r), International Physical Activity Questionnaire (IPAQ) and the Walter Reed Visual Assessment Scale.
Curve severity at end of study.
Curve severity measured as Cobb angle at end of study.
Health economic evaluations; actual cost for a treatment
Actual analysis of direct costs, and estimations of indirect costs.

Full Information

First Posted
December 28, 2012
Last Updated
October 13, 2023
Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital, Region Stockholm, The Swedish Research Council, University Hospital, Linkoeping
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1. Study Identification

Unique Protocol Identification Number
NCT01761305
Brief Title
Trial on Three Treatments for Scoliosis
Acronym
CONTRAIS
Official Title
CONTRAIS: CONservative TReatment for Adolescent Idiopathic Scoliosis. A Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2013 (undefined)
Primary Completion Date
August 29, 2021 (Actual)
Study Completion Date
December 2030 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital, Region Stockholm, The Swedish Research Council, University Hospital, Linkoeping

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Idiopathic scoliosis is a three-dimensional structural deformity of the spine that occurs in children. Recent reviews on bracing and exercise treatment have provided some evidence for effect of these interventions. The purpose of this study is to compare the effectiveness of night time bracing, scoliosis specific exercises and physical activity prescription in adolescents with idiopathic scoliosis.
Detailed Description
Today, bracing is used to prevent progression of idiopathic scoliosis in children. The evidence for bracing and physical activity for treatment of idiopathic scoliosis is poor. Only one low quality study has compared bracing with physical exercise, showing no statistical differences in the reduction or progression of scoliosis curves between the groups. To draw valid conclusions about the effectiveness of postural specific physical exercise and brace therapeutic interventions compared to a self mediated activity exercise group, a randomized controlled trial research design will be used. Preliminary data suggests that approximately 8 hours of night-time bracing with an over-corrective brace is as effective as bracing during 23 hours per day. Night-time bracing is attractive since you wear the brace a limited amount of time. Several theories propose that during the adolescent period of skeletal growth, bone deformation may occur due to a combination of asymetrical growth plate activity, vertebral body weakness or an imbalance of muscle forces and joint flexibility. An association between low bone mineral density and idiopathic scoliosis has been reported in the literature. Adequate physical activity levels is a requirement for normal growth and development during childhood and adolescents. It is well documented that physical exercise is associated with improvements in not only muscle strength, aerobic fitness and motor development but also bone density which may help decrease the risk of osteopenic related bone deformation. Patients included in the study will be randomized to one of three groups. Each of the three groups will receive a physical activity prescription according to World Health Organisation recommendations. One group will additionally wear a hyper-corrective night-time brace. One group will additionally perform postural scoliosis-specific exercises. Patients not wanting to be randomized to the alternative treatments in the clinical trial will receive bracing which is the current standard treatment offered. The purpose of the study is to compare the risk of curve progression in the different groups. Curve progression is measured on x-rays. Participation in the study will last until the curve has progressed, or until cessation of skeletal growth. Participants with braces will be instructed to wear the brace 8 hours per night. Participants receiving scoliosis specific training will receive 3x90 minute physiotherapist guided sessions with an additional session provided every 6 months for the entirety of the study. All participants will be recommended to be physically active at least 60 minutes per day.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Scoliosis
Keywords
Idiopathic scoliosis, Brace, Scoliosis specific exercise, Physical activity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
135 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Brace
Arm Type
Experimental
Arm Description
Hypercorrective night-time brace worn 8 hours per night. A prescription of general physical activity will be provided at a dose of 60 minutes per day. Instructions regarding physical activity will be delivered during a one hour session.
Arm Title
Scoliosis specific exercises.
Arm Type
Experimental
Arm Description
Scoliosis specific exercises. The intervention will be delivered in 3 x 90 minute sessions, once per month during the first 3 months. An additional session will be provided every 6 months for the entirety of the study. A prescription of general physical activity will be provided at a dose of 60 minutes per day.
Arm Title
Self-mediated physical activity.
Arm Type
Active Comparator
Arm Description
A prescription of general physical activity will be provided at a dose of 60 minutes per day. Instructions will be delivered during a 1 hour session.
Intervention Type
Procedure
Intervention Name(s)
Hypercorrective night-time brace
Intervention Description
Hypercorrective night-time brace worn 8 hours per night. Patients are encouraged to also continue with non-specific self-mediated physical activities of moderate intensity at least 60 minutes daily, for the entirety of the study. Reinforcement of the assigned intervention will be performed in conjunction with reassessment every 6 months. A training diary will be implemented to follow and motivate the patient's training behaviour.
Intervention Type
Behavioral
Intervention Name(s)
Scoliosis specific exercises.
Intervention Description
The intervention will be delivered in 3 x 90 minute sessions, once per month during the first 3 months. Goals are directed towards active self-correction and postural control, spinal stability, aerobic functioning and development of a positive body image. Additional postural specific exercises including self-mediated hyper-corrective exercises are to be performed with moderate intensity at least for 30 minutes at least 2-3 times per week. Other physical activities to fulfill the general recommended quota of more than 60 minutes moderate intensity physical activity per day are recommended. Reinforcement of the intervention will be performed in conjunction with reassessment every 6 months. A training diary will be implemented to follow and motivate the patient's training behaviour.
Intervention Type
Other
Intervention Name(s)
Self-mediated physical activity.
Intervention Description
Instructions for self-mediated physical activity will be delivered during a 1 hour session. Patients are encouraged to perform self-mediated physical activities of moderate intensity at least 60 minutes daily, for the entirety of the study. Reinforcement of the assigned intervention will be performed in conjunction with reassessment every 6 months. A training diary will be implemented to follow and motivate the patient's training behaviour.
Primary Outcome Measure Information:
Title
Radiological progression of scoliosis
Description
Progression of the Cobb angle more than 6 degrees, compared to the primary x-ray, seen on two consecutive spinal standing x-rays.
Time Frame
Measured every 6 months, for an expected average of three years
Secondary Outcome Measure Information:
Title
Quality of life assessed with questionnaire instruments
Description
Quality of life measured with validated questionnaires such as Euroqol (EQ5D-Y), Scoliosis Research Society outcomes questionnaire 22r (SRS22r), International Physical Activity Questionnaire (IPAQ) and the Walter Reed Visual Assessment Scale.
Time Frame
Measured every 6 months, for an expected average of three years
Title
Curve severity at end of study.
Description
Curve severity measured as Cobb angle at end of study.
Time Frame
Measured at end of study, expected at an average of three years after study inclusion
Title
Health economic evaluations; actual cost for a treatment
Description
Actual analysis of direct costs, and estimations of indirect costs.
Time Frame
Measured at end of study, expected an average of three years after study inclusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of idiopathic scoliosis Skeletally immature with estimated remaining growth for at least one year. Not more than one year after menarche Primary Cobb angle between 25 and 40 degrees. Curve apex T7 or caudal Exclusion Criteria: Scoliosis with a possible non-idiopathic ethiology. Patients will be excluded from the study if the pathogenesis of the scoliosis is not idiopathic, but due to a neuromuscular, neurological, congenital malformation or trauma related comorbidity. Previous brace or surgical treatment for scoliosis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Gerdhem, MD, PhD
Organizational Affiliation
Karolinska Institutet, Karolinska University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Allan Abbott, MPhyt, PhD
Organizational Affiliation
Linköping University- Sweden, Linköping and Karolinska University Hospital - Sweden
Official's Role
Study Director
Facility Information:
Facility Name
Mälarsjukhuset / Eskilstuna hospital
City
Eskilstuna
ZIP/Postal Code
63188
Country
Sweden
Facility Name
Ryhov Hospital
City
Jönköping
ZIP/Postal Code
55185
Country
Sweden
Facility Name
Linköping University, Linköping University Hospital
City
Linköping
ZIP/Postal Code
58183
Country
Sweden
Facility Name
Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
14186
Country
Sweden
Facility Name
Sundsvall Hospital
City
Sundsvall
ZIP/Postal Code
85186
Country
Sweden
Facility Name
Umeå University, Norrland University Hospital
City
Umeå
ZIP/Postal Code
90185
Country
Sweden
Facility Name
Västerås Hospital
City
Västerås
ZIP/Postal Code
72189
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified manuscript data.
IPD Sharing Time Frame
At the time of publication
IPD Sharing Access Criteria
Data will be made available upon reasonable request.
Citations:
PubMed Identifier
24007599
Citation
Abbott A, Moller H, Gerdhem P. CONTRAIS: CONservative TReatment for Adolescent Idiopathic Scoliosis: a randomised controlled trial protocol. BMC Musculoskelet Disord. 2013 Sep 5;14:261. doi: 10.1186/1471-2474-14-261.
Results Reference
derived

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Trial on Three Treatments for Scoliosis

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