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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06219772
Other study ID # ECM#2023-2105
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2024
Est. completion date August 2024

Study information

Verified date April 2024
Source Cairo University
Contact Doaa A Elimy, lecturer
Phone 00201066474654
Email do3aayoub25@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess dynamic balance in females with adolescent idiopathic scoliosis compared to normal subjects.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date August 2024
Est. primary completion date August 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 10 Years to 20 Years
Eligibility Inclusion Criteria: 1. Females with age between 10-20 years. 2. Idiopathic scoliosis will be diagnosed based on clinical examination and radiological measures. 3. Cobb's angle will be between 20° and 40°. 4. Their BMI from 18 to 24.9 kg/m2. 5. They must be willing to participate in the study. Exclusion Criteria: 1. History of previous back surgery. 2. Neurological deficit. 3. Current lower extremity symptoms. 4. Symptoms of vertigo or dizziness. 5. No other disorders in the vertebral column (disc prolapse, spondylosis, fracture).

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Doaa Ayoub Elimy Cairo

Sponsors (2)

Lead Sponsor Collaborator
Cairo University King Khalid University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dynamic balance A Biodex balance system will be used for measuring the dynamic balance. Through study completion, an average of 7 months
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