Clinical Trials Directory

Trials / Completed

CompletedNCT06812013

Impact of Idiopathic Scoliosis on Balance and Footprint Symmetry in Adolescents

Status
Completed
Phase
Study type
Observational
Enrollment
150 (actual)
Sponsor
Al-Zaytoonah University of Jordan · Academic / Other
Sex
All
Age
10 Years – 18 Years
Healthy volunteers
Accepted

Summary

Adolescent idiopathic scoliosis (AIS) is the most prevalent form of scoliosis that affects children after the age of 10 years and is considered a critical developmental stage of the musculoskeletal system of the child. AIS causes deviations in the CNS, leading to asymmetry of motor activity and, consequently, an incorrect position of the spine. The progressive deformation of the spine leads to increased asymmetry in body functions. This elevated asymmetry is understood by the nervous system as a norm, which causes children to cease to sense the correct body position that may affect both static and dynamic balance and the foot pressure symmetry of the child, which was not investigated in such cases in any previous studies till now.

Conditions

Interventions

TypeNameDescription
OTHERassessment of foot print and balanceFor static and dynamic balance assessment, Biodex Medical Systems Inc., Shirley, New York, USA (serial n.: 13020193) was used. The device consists of a circular foot platform that permits tilting in all directions, height-adjustable support rails, height adjustable display screen, and a printer. Balance assessment by the Biodex system is a valid and reliable objective measurement. For assessment of foot print symmetry Tekscan HR walkway Mat™ pressure measurement system, Tekscan Inc. USA will be use. It is made up of a digital mat inserted into a wooden walkway, sensors (4 senses/cm2) embedded in the mat, and a computer running the Tekscan Software (version 7) for data extrapolation.

Timeline

Start date
2025-02-10
Primary completion
2025-05-05
Completion
2025-05-08
First posted
2025-02-06
Last updated
2025-05-09

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06812013. Inclusion in this directory is not an endorsement.