NCT06219772

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 12, 2024

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 23, 2024

Completed
9 days until next milestone

Study Start

First participant enrolled

February 1, 2024

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2024

Completed
Last Updated

September 23, 2024

Status Verified

September 1, 2024

Enrollment Period

7 months

First QC Date

January 12, 2024

Last Update Submit

September 19, 2024

Conditions

Keywords

adolescent idiopathic scoliosisdynamic balanceCobb anglestability index

Outcome Measures

Primary Outcomes (1)

  • Dynamic balance

    A Biodex balance system will be used for measuring the dynamic balance.

    Through study completion, an average of 7 months

Eligibility Criteria

Age10 Years - 20 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodProbability Sample
Study Population

Adolescent idiopathic scoliosis and normal subjects

You may qualify if:

  • 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.

You may not qualify if:

  • 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).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Doaa Ayoub Elimy

Cairo, Egypt

Location

Study Officials

  • Ghada MR Koura, Ass. prof

    King Khalid University, Saudi Arabia

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of physical therapy for basic science department., faculty of physical Therapy

Study Record Dates

First Submitted

January 12, 2024

First Posted

January 23, 2024

Study Start

February 1, 2024

Primary Completion

August 31, 2024

Study Completion

August 31, 2024

Last Updated

September 23, 2024

Record last verified: 2024-09

Locations