- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06219772
Assessment of Dynamic Balance in Idiopathic Scoliosis Compared to Normal Subjects
Assessment of Dynamic Balance in Females With Adolescent Idiopathic Scoliosis Compared to Normal Subjects: A Comparative Study
Study Overview
Status
Conditions
Detailed Description
Adolescent idiopathic scoliosis (AIS) is one of the most common forms of scoliosis. It is a three-dimensional deformity of the spine and trunk with a lateral deviation of ≥ 10°, which can occur during the growing years from 10 years to puberty, with an apparent gender dominance rising with age and severity with a female to male ratio of 1.5:1 to 10:1.
Dynamic balance is the ability to maintain and regain the center of gravity within the base of support in response to outside perturbations or voluntary movements. It has been reported that AIS is associated with trunk imbalance and could negatively influence the sensorimotor control of posture and decrease postural balance capabilities, which increases susceptibility to injuries and impacts the individual's ability to engage in daily living activities.
Previous research reported that postural stability control in adolescents with idiopathic scoliosis is as good as in healthy individuals, and others found that AIS patients have poorer static balance control than age-matched patients without AIS. So the current study will be conducted to investigate the dynamic balance in females with adolescent idiopathic scoliosis compared to normal subjects.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Cairo, Egypt
- Doaa Ayoub Elimy
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Females with age between 10-20 years.
- Idiopathic scoliosis will be diagnosed based on clinical examination and radiological measures.
- Cobb's angle will be between 20° and 40°.
- Their BMI from 18 to 24.9 kg/m2.
- They must be willing to participate in the study.
Exclusion Criteria:
- History of previous back surgery.
- Neurological deficit.
- Current lower extremity symptoms.
- Symptoms of vertigo or dizziness.
- No other disorders in the vertebral column (disc prolapse, spondylosis, fracture).
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Dynamic balance
Time Frame: Through study completion, an average of 7 months
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A Biodex balance system will be used for measuring the dynamic balance.
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Through study completion, an average of 7 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Ghada MR Koura, Ass. prof, King Khalid University, Saudi Arabia
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ECM#2023-2105
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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