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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03391895
Other study ID # BVUgbasbug01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 23, 2018
Est. completion date June 26, 2018

Study information

Verified date June 2018
Source Bezmialem Vakif University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Scoliosis is the abnormality of the spine with direct effects on the shape and mechanics of the thoracic cage. Adolescent Idiopathic Scoliosis (AIS) is the most common 3-dimensional deformity of the spine which can potentially affect respiratory function, exercise capacity as well as the performance of inspiratory and expiratory muscles. During growth morphological changes of thoracic cage affects the pulmonary tissues and functions. Respiratory functions shows negative changes due to Cobb angle, curve localization, number of vertebra and onset age in patient with scoliosis.

Exercise approaches include respiratory training program and aim to improve respiratory functions.It is reported that respiratory muscle weakness is a potent contributor to pulmonary impairment in mild, moderate, and severe forms of scoliosis. Studies showed that exercise training and respiratory exercises may improve respiratory function and exercise capacity in patients with AIS. Thus the aim of this study was to investigate the effect of inspiratory muscle training on respiratory muscle strength, respiratory function and functional capacity in adolescents with idiopathic scoliosis.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date June 26, 2018
Est. primary completion date June 21, 2018
Accepts healthy volunteers No
Gender All
Age group 10 Years to 18 Years
Eligibility Inclusion Criteria:

- Adolescent Idiopathic Scoliosis diagnosis

Exclusion Criteria:

- Documented diagnosis any of cardiopulmonary, neurological, orthopedic or mental disorders which may affect the assessment results.

- Subjects previously involved in exercise training or physiotherapy programs

- Subjects previously undertaken any of spinal surgeries.

Study Design


Intervention

Other:
Home based exercise program
Program will include deep diaphragmatic breathing exercises, local expansion exercise on the collapsed areas in scoliosis concave sides with elastic exercise bands, dynamic lumber stabilization exercises for core stabilisation, strengthening of interscapular muscles with elastic bands and stretching exercises for lumbar extensor, hip flexor and hamstring muscles. Exercises will be applied 2 sets of 10 repetitions and once a day.
Inspiratory Muscle Training
Threshold IMT device will be used for the training. Training intensity will set at 30% of the maximum inspiratory pressure after assessment of respiratory muscle strength for each patient every week.

Locations

Country Name City State
Turkey Bezmialem Vakif University Istanbul

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 Peak Expiratory Flow (PEF) at 8 weeks Eight weeks
Primary Change from baseline Maximum Inspiratory Pressure (MIP) at 8 weeks Eight weeks
Primary Change from baseline Maximum Expiratory Pressure (MEP) 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 thoracic axial trunk rotation (ATR) Measurements will be applied with Bunnell Scoliometer by a qualified physiotherapist. Eight weeks
Secondary Change from baseline thoracic-lumber junction axial trunk rotation (ATR) Measurements will be applied with Bunnell Scoliometer by a qualified physiotherapist. Eight weeks
Secondary Change from baseline lumber axial trunk rotation (ATR) Measurements will be applied with Bunnell Scoliometer by a qualified physiotherapist. Eight weeks
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