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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03823053
Other study ID # BVUsyildirim01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 25, 2019
Est. completion date June 28, 2019

Study information

Verified date November 2020
Source Bezmialem Vakif University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The vertebral column is a structure that transfers the weight of the head and torso to the lower extremity, provides trunk movements and protects the spinal cord.A three dimensional deformity involving lateral flexion of the vertebrae in the frontal plane at 10 ° and above, including axial rotation and physiologic flexion (hypokyphosis) components in the sagittal plane, is defined as scoliosis. Adolescent idiopathic scoliosis (AIS) is a type of idiopathic scoliosis that occurs in the period from the onset of puberty (up to 10 years) until the closure of growth plates. Scoliosis is caused by postural, balance and neuromotor disorders as a primary cause of impaired sensory integrity, proprioceptive feedback deficits, secondary lung problems, organ disorders and pain. In addition, the quality of life in these individuals is also seen to decrease.Children with adolescent idiopathic scoliosis have inadequate respiratory function and a decrease in functional capacity. At the same time, these children show muscle weakness in certain parts of the body. The aim of this study was to investigate the relationship between home based core stabilization training, respiratory parameters, peripheral muscle strength, balance, functional capacity and quality of life in individuals with young scoliosis. The investigators suggest that the addition of core stabilization training to children with mild and moderate adolescent idiopathic scoliosis will produce good results.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 28, 2019
Est. primary completion date June 21, 2019
Accepts healthy volunteers No
Gender All
Age group 10 Years to 24 Years
Eligibility Inclusion Criteria: - Adolescent Idiopathic Scoliosis diagnosis Exclusion Criteria: - Documented diagnosis any of cardiopulmonary, neurological, orthopedic or mental disorders which may affect the assessments results. - Subjects previously undertaken any of spinal surgeries. - Subjects involved in exercise training 3 or more days a week.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Home Based Traditional Scoliosis Exercise
Program will include posture exercises, strengthening exercises of interscapular muscle and limb, diaphragmatic breathing exercises and stretching exercises for lumbar extensor, hip flexor, hamstring, pectoral muscles. Exercises will be applied 1 sets of 10 repetitions and once a day.
Home Based Core Stabilization Training
Program will include posture exercises, strengthening exercises of interscapular muscle and limb, diaphragmatic breathing exercises and stretching exercises for lumbar extensor, hip flexor, hamstring, pectoral muscles. In addition, the training group received core stabilization exercises for multifidus, transversus abdominis, diaphragm,erector spines, rectus abdominis, internal and external obliques, quadratus lumborum, gluteus maximus, and pelvic floor muscles.Exercises will be applied 1 sets of 10 repetitions and once a day.

Locations

Country Name City State
Turkey Bezmialem Vakif University Istanbul Eyüp

Sponsors (1)

Lead Sponsor Collaborator
Bezmialem Vakif University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline Forced Vital Capacity (FVC) at 8 weeks Eight weeks
Primary Change from baseline Forced Expiratory volume in 1 second (FEV1)at 8 weeks Eight weeks
Primary Change from baseline Peripheral Muscle strength at 8 weeks Eight weeks
Primary Change from baseline Balance at 8 weeks Eight weeks
Primary Change from baseline distance covered in Six- Minute Walk Test at 8 weeks Eight weeks
Secondary Change from baseline axial trunk rotation (ATR) Measurements will be applied with Bunnell Scoliometer by physiotherapist. Eight weeks
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