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Scoliosis-specific Exercises for Mild Idiopathic Scoliosis

Primary Purpose

Idiopathic Scoliosis

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Active self-corrective exercises
Observation
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, Randomized controlled trial, Exercise, Rehabilitation, Self-correction

Eligibility Criteria

9 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cobb 15-24 degrees
  • Skeletally immature, Sanders score of 4 or less and Risser < 2.
  • No menarche for females
  • Aged 9-15 years
  • Apex of the primary curve at T7 or caudal

Exclusion Criteria:

  • Non-idiopathic scoliosis (i.e. neuromuscular, syndromic or congenital scoliosis)
  • No previous surgical or brace treatment for scoliosis

Sites / Locations

  • Linköping university hospitalRecruiting
  • Karolinska university hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Active self-corrective exercises

Observation

Arm Description

An active self-correction tailored to the individual type of curve and clinical presentation will be applied with the aim to correct the scoliosis in all three planes. Patients will also be informed and educated in task oriented activities of daily living. Training goals are directed towards postural control, spinal stability, muscular stabilization and endurance in corrective postures. Patients will have outpatient sessions once every two weeks the first 3 months and perform the exercises at home in 30-minutes sessions three times per week. Patients are encouraged to continue with non-specific self-mediated physical activities of moderate intensity at least 60 minutes daily. Compliance will be monitored through a mobile application (Physitrack) where the patients record their sessions and can have contact with the research personnel. A cognitive behavioral therapy approach to reinforce physical activity will be performed every 6 months.

Patients are encouraged to continue with non-specific self-mediated physical activities of moderate intensity at least 60 minutes daily, for the entirety of the study. A cognitive behavioral therapy approach to reinforce physical activity will be performed every 6 months.

Outcomes

Primary Outcome Measures

Number of patients progressing in curve severity
Increase in curve severity (Cobb angle) of more than 6 degrees on two consecutive full-spine frontal radiographs as compared with baseline

Secondary Outcome Measures

Angle of trunk rotation
Angle of trunk rotation in forward bending, assessed according to Adams forward bending test with Bunnell's scoliometer
Patient-reported outcome measures
Scoliosis Research Society-22r questionnaire (SRS-22r) ranging from 1 (worst) to 5 (best)
Patient-reported outcome measures
The child-friendly EQ-5D version (EQ-5D-Y) with values ranging from 1 (best) to 3 (worst)
Patient-reported outcome measures
Pictorial part of Spinal Appearance Questionnaire (pSAQ) with values ranging from 7 (best) to 35 (worst)
Patient-reported outcome measures
International Physical Activity Questionnaire-short form (IPAQ-SF) where data will be presented as energy expenditure, Metabolic Equivalent Task (MET) minutes, and proportion of individuals reaching moderate activity level. Moderate activity level is considered if 3 or more days of vigorous activity of at least 20 minutes per day, 5 or more days of moderate-intensity activity and/or walking of at least 30 minutes per day, or 5 or more days of any combination of walking, moderate-intensity, or vigorous-intensity activities accumulating at least 600 MET-minutes per week
Brace treatment
Number of patients needing brace treatment. Indication for brace treatment is progression of more than 6 degrees on standing frontal radiograph and a primary curve surpassing 25 degrees.

Full Information

First Posted
November 5, 2021
Last Updated
October 13, 2023
Sponsor
Karolinska Institutet
Collaborators
Linkoeping University
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1. Study Identification

Unique Protocol Identification Number
NCT05138393
Brief Title
Scoliosis-specific Exercises for Mild Idiopathic Scoliosis
Official Title
PREventing Mild Idiopathic SCOliosis PROgression (PREMISCOPRO): a Randomized Controlled Trial Comparing Scoliosis-specific Exercises to Observation in Mild Idiopathic Scoliosis
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 18, 2022 (Actual)
Primary Completion Date
November 30, 2027 (Anticipated)
Study Completion Date
November 30, 2037 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Linkoeping University

4. Oversight

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

5. Study Description

Brief Summary
Idiopathic scoliosis is the most common spinal deformity in children and adolescents with an estimated prevalence of 3%. About one tenth of the children with scoliosis develop a deformity that requires treatment with brace or surgery with the current treatment protocol. In Sweden, mild scoliosis curves not requiring treatment, but at risk for progression during childhood, are only observed until skeletal maturity without active treatment. If progression occurs and treatment is required, standard treatment consists of bracing 20 hours or more per day. Scoliosis-specific exercises have been reported to be a possible treatment modality in terms of halting progression in mild scoliosis, but the findings are not generally accepted.
Detailed Description
Mild forms of idiopathic scoliosis are usually observed with regular clinical and radiological follow-ups during growth periods. Scoliosis specific exercises have been used as a method aiming to halt progression and ultimately avoid the need of brace treatment. However, many cases of mild idiopathic scoliosis will not progress irrespective of treatment. As of today, there are a number of different methods and approaches to scoliosis specific exercises, but all with the aim to correct scoliosis in the sagittal, frontal and transverse plane. In a multicenter randomized controlled trial, the investigators seek to compare an active self corrective management of scoliosis specific exercises to observation for patients with mild scoliosis. Skeletally immature patients with mild idiopathic scoliosis will be randomized in an online module through the Swedish spine register (www.swespine.se), to receive either the intervention or observation. Outcome assessors will be blinded for the type of management the patients are having. Compliance will be monitored with a mobile application (Physitrack) where the patients and their families can have direct access to the research personnel and their treatment. Outcome measures include changes in curve severity, quality of life, number of patients requiring brace treatment and clinical outcomes. All patients will be evaluated with clinical follow-ups every six months and both clinical and radiological follow-ups each twelve months until either progression occurs or skeletal maturity is reached. Individuals progressing and requiring brace treatment will be offered standard TLSO or nighttime brace to be worn 20 hours and 8 hours, respectively, per day and will be followed in the same way as other participants. Skeletal maturity is defined as less than 1 cm of growth in six months. All patients will be encouraged to be physically active for 60 minutes per day. When skeletal maturity has occured, patients will have clinical and radiological follow-ups at 2, 5 and 10 years after treatment termination. Based on a hypothesized failure rate of 10% in the scoliosis specific exercise group and 39% in the observation group, with a significance level of 5% and a power of 80% and consideration for dropout of up to 20% and an additional adding of five individuals per group, an estimated number of 45 individuals in each group is required. For individuals who are not willing to be randomized and participate in the study, observation will be offered and these individuals will serve as an observational group with similar follow-ups and will be asked to answer the same survey as the study groups will do.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Scoliosis
Keywords
Idiopathic scoliosis, Randomized controlled trial, Exercise, Rehabilitation, Self-correction

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Active self-corrective exercises
Arm Type
Experimental
Arm Description
An active self-correction tailored to the individual type of curve and clinical presentation will be applied with the aim to correct the scoliosis in all three planes. Patients will also be informed and educated in task oriented activities of daily living. Training goals are directed towards postural control, spinal stability, muscular stabilization and endurance in corrective postures. Patients will have outpatient sessions once every two weeks the first 3 months and perform the exercises at home in 30-minutes sessions three times per week. Patients are encouraged to continue with non-specific self-mediated physical activities of moderate intensity at least 60 minutes daily. Compliance will be monitored through a mobile application (Physitrack) where the patients record their sessions and can have contact with the research personnel. A cognitive behavioral therapy approach to reinforce physical activity will be performed every 6 months.
Arm Title
Observation
Arm Type
Active Comparator
Arm Description
Patients are encouraged to continue with non-specific self-mediated physical activities of moderate intensity at least 60 minutes daily, for the entirety of the study. A cognitive behavioral therapy approach to reinforce physical activity will be performed every 6 months.
Intervention Type
Other
Intervention Name(s)
Active self-corrective exercises
Intervention Description
Scoliosis specific exercises with an Active self-corrective approach. Non-specific physical activity 60 minutes per day.
Intervention Type
Other
Intervention Name(s)
Observation
Intervention Description
Non-specific physical activity 60 minutes per day.
Primary Outcome Measure Information:
Title
Number of patients progressing in curve severity
Description
Increase in curve severity (Cobb angle) of more than 6 degrees on two consecutive full-spine frontal radiographs as compared with baseline
Time Frame
Measured at each radiological (annual) follow-up until skeletal maturity. Skeletal maturity is defined as less than 1 cm body height increase in 6 months
Secondary Outcome Measure Information:
Title
Angle of trunk rotation
Description
Angle of trunk rotation in forward bending, assessed according to Adams forward bending test with Bunnell's scoliometer
Time Frame
At each six-month follow-up and at 2, 5, 10 years after skeletal maturity
Title
Patient-reported outcome measures
Description
Scoliosis Research Society-22r questionnaire (SRS-22r) ranging from 1 (worst) to 5 (best)
Time Frame
At each six-months follow-up and 2, 5, 10 years after skeletal maturity
Title
Patient-reported outcome measures
Description
The child-friendly EQ-5D version (EQ-5D-Y) with values ranging from 1 (best) to 3 (worst)
Time Frame
At each six-month follow-up and 2, 5, 10 years after skeletal maturity
Title
Patient-reported outcome measures
Description
Pictorial part of Spinal Appearance Questionnaire (pSAQ) with values ranging from 7 (best) to 35 (worst)
Time Frame
At each six-month follow-up, and 2, 5, 10 years after skeletal maturity
Title
Patient-reported outcome measures
Description
International Physical Activity Questionnaire-short form (IPAQ-SF) where data will be presented as energy expenditure, Metabolic Equivalent Task (MET) minutes, and proportion of individuals reaching moderate activity level. Moderate activity level is considered if 3 or more days of vigorous activity of at least 20 minutes per day, 5 or more days of moderate-intensity activity and/or walking of at least 30 minutes per day, or 5 or more days of any combination of walking, moderate-intensity, or vigorous-intensity activities accumulating at least 600 MET-minutes per week
Time Frame
At each six-month follow-up, and 2, 5, 10 years after skeletal maturity
Title
Brace treatment
Description
Number of patients needing brace treatment. Indication for brace treatment is progression of more than 6 degrees on standing frontal radiograph and a primary curve surpassing 25 degrees.
Time Frame
At each six-months follow-up and 2, 5, 10 years after skeletal maturity

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cobb 15-24 degrees Skeletally immature, Sanders score of 4 or less and Risser < 2. No menarche for females Aged 9-15 years Apex of the primary curve at T7 or caudal Exclusion Criteria: Non-idiopathic scoliosis (i.e. neuromuscular, syndromic or congenital scoliosis) No previous surgical or brace treatment for scoliosis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elias Diarbakerli, PT, PhD
Phone
+460851770000
Email
elias.diarbakerli@regionstockholm.se
First Name & Middle Initial & Last Name or Official Title & Degree
Paul Gerdhem, MD, PhD
Email
paul.gerdhem@uu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elias Diarbakerli, PT, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Linköping university hospital
City
Linköping
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Allan Abbott, PT, PhD
Facility Name
Karolinska university hospital
City
Stockholm
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elias Diarbakerli, PT, PhD
First Name & Middle Initial & Last Name & Degree
Paul Gerdhem, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
IPD underlying published manuscripts will be accessible for other researchers.
IPD Sharing Time Frame
The study protocol will be submitted to a peer-reviewed journal.
IPD Sharing Access Criteria
The investigators in charge will be responsible for reviewing access requests. Crude data, randomization procedures and intervention details can be shared with other researchers upon request.

Learn more about this trial

Scoliosis-specific Exercises for Mild Idiopathic Scoliosis

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