Effect of Lyon and Schroth Techniques on Adolescent İdiopathic Scoliosis
Primary Purpose
Adolescent Idiopathic Scoliosis
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Schroth Treatment
Sponsored by
About this trial
This is an interventional treatment trial for Adolescent Idiopathic Scoliosis
Eligibility Criteria
Inclusion Criteria:
- Participants were between ages 10-18,
- Volunteered for the study,
- Diagnosed with adolescent idiopathic scoliosis,
- Cobb angle between 10-30 degrees,
- 0-3 Risser sign,
- Sanders classification 0-4 ,
- Lenke curve type 1
Exclusion Criteria:
- Participants who other type of scoliosis
- Previous spinal surgery
- Exercise contraindications
- Rheumatological disease
- Another neuromuscular problem were excluded from the study.
Sites / Locations
- Kırşehir Ahi Evran University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Scoliosis Treatment Group
Lyon Treatment
Arm Description
For the scoliosis group treatment include schroth theraphy
For the scoliosis group treatment include Lyon theraphy..
Outcomes
Primary Outcome Measures
Cobb angle
Cobb measurement
Secondary Outcome Measures
Scoliosis research society-22
Quality of life
Full Information
NCT ID
NCT05223972
First Posted
January 12, 2022
Last Updated
August 7, 2023
Sponsor
Kirsehir Ahi Evran Universitesi
1. Study Identification
Unique Protocol Identification Number
NCT05223972
Brief Title
Effect of Lyon and Schroth Techniques on Adolescent İdiopathic Scoliosis
Official Title
The Comparasion Effect of Lyon and Schroth Techniques on Adolescent İdiopathic Scoliosis
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
March 10, 2022 (Actual)
Primary Completion Date
June 12, 2022 (Actual)
Study Completion Date
June 30, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kirsehir Ahi Evran Universitesi
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
Today, it is known that the conservative treatment of scoliosis is gaining importance. In addition, no study has been found comparing the efficacy of two important conservative treatment methods, the Schroth and Lyon method, in adolescent idiopathic scoliosis. Accordingly, this study was conducted to compare the effectiveness of schroth and Lyon exercises in individuals with AIS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescent Idiopathic Scoliosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
34 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Scoliosis Treatment Group
Arm Type
Experimental
Arm Description
For the scoliosis group treatment include schroth theraphy
Arm Title
Lyon Treatment
Arm Type
Experimental
Arm Description
For the scoliosis group treatment include Lyon theraphy..
Intervention Type
Other
Intervention Name(s)
Schroth Treatment
Other Intervention Name(s)
Lyon Treatment
Intervention Description
Schroth exercises consist of passive and active postural auto-correction exercises done repeatedly and based on kinesthetic and sensorimotor principles. The ultimate goal of the Schroth method is to enable the patient to consciously maintain correct posture in their daily living activities. To achieve this requires repeating corrective movements performed to improve postural motor control. Schroth exercises also include strength and endurance training of postural muscles in order to improve the curve, raise the patient's self-image, and reduce pain. In this study, the Schroth exercises progressed from more to less passive support, from more to less feedback, and from lying to sitting or standing positions, according to the patient's ability to perform the specific exercise
Primary Outcome Measure Information:
Title
Cobb angle
Description
Cobb measurement
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Scoliosis research society-22
Description
Quality of life
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Participants were between ages 10-18,
Volunteered for the study,
Diagnosed with adolescent idiopathic scoliosis,
Cobb angle between 10-30 degrees,
0-3 Risser sign,
Sanders classification 0-4 ,
Lenke curve type 1
Exclusion Criteria:
Participants who other type of scoliosis
Previous spinal surgery
Exercise contraindications
Rheumatological disease
Another neuromuscular problem were excluded from the study.
Facility Information:
Facility Name
Kırşehir Ahi Evran University
City
Kırşehir
ZIP/Postal Code
40100
Country
Turkey
12. IPD Sharing Statement
Learn more about this trial
Effect of Lyon and Schroth Techniques on Adolescent İdiopathic Scoliosis
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