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This Cross-sectional Study Investigates the Relationship Between Different Curve Patterns in Adolescent Idiopathic Scoliosis (AIS) and the Distribution of Foot Pressure. It Aims to Determine Whether Coronal and Sagittal Curve Patterns Are Associated With Asymmetries in Plantar Pressure Distribution

NCT07172048 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 84

Last updated 2025-09-15

No results posted yet for this study

Summary

This cross-sectional study investigates the relationship between different curve patterns in Adolescent Idiopathic Scoliosis (AIS) and the distribution of foot pressure. It aims to determine whether coronal and sagittal curve patterns are associated with asymmetries in plantar pressure distribution during static standing.

Conditions

  • Scoliosis Idiopathic

Interventions

DIAGNOSTIC_TEST

Foot pressure Distribution test

This study is observational and does not involve any therapeutic or experimental intervention. Participants will be divided into two groups based on their scoliosis curve pattern: Group 1: Adolescents with a major thoracic curve. Group 2: Adolescents with a major lumbar curve. Each participant will undergo non-invasive assessments including: Baropodometric foot pressure analysis during static standing to evaluate pressure distribution in both coronal and sagittal planes. Radiographic evaluation to classify curve patterns using Cobb's angle, Central Sacral Vertical Line, and Plumb Line.

Sponsors & Collaborators

  • Advanced Rehabilitation Center, Egypt

    collaborator OTHER

  • Mahmoud Ibrahim Elsayed Aly Mahmoud

    lead OTHER

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-08-01
Primary Completion
2025-10-30
Completion
2025-10-30

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07172048 on ClinicalTrials.gov