NCT06802653

Brief Summary

The purpose of this study is to investigate the prevalence and etiology of adolescent idiopathic scoliosis in the Nanchang region. Elementary and middle school students who met the inclusion criteria were included in the study and school-based scoliosis screening was conducted. Diagnosis of suspected scoliosis was determined by physical examination, Adams forward bend test, measurement of trunk rotation angle, and Standing Anteroposterior X-ray of the Spine. The prevalence of suspected scoliosis among elementary and middle school students was calculated. At the same time, the researchers kept detailed records of all costs incurred in the school screening.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 26, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 31, 2025

Completed
6 months until next milestone

Study Start

First participant enrolled

July 28, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 15, 2025

Completed
13 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 28, 2025

Completed
Last Updated

May 30, 2025

Status Verified

March 1, 2025

Enrollment Period

2 months

First QC Date

January 26, 2025

Last Update Submit

May 25, 2025

Conditions

Keywords

scoliosisscreeningadolescentsprevalencecost of screening

Outcome Measures

Primary Outcomes (4)

  • Footscan Plantar Pressure Test Parameters

    The results of the Footscan plantar pressure test parameters for participants included total pressure on the left foot, total pressure on the right foot, forefoot pressure on both sides, and hindfoot pressure on both sides.

    The process from enrollment to the completion of screening takes about one week.

  • Physical Examination

    The examinee has a bare back, stands naturally, feet shoulder-width apart, eyes flat, arms down, palms facing inward. The examiner observes whether the patient's shoulders are equal in height; whether the angles of both subscapularis are at the same level; whether the lumbar concavity is symmetrical on both sides; whether the iliac crests are equal in height bilaterally; and whether the spinous processes are deviating from the median axis.

    The process from enrollment to the completion of screening takes about one week.

  • standing anteroposterior X-rays of the spine

    Information from standing anteroposterior X-rays of the spine, including Cobb angle, Risser grade, Nash-Moe grade, and curve type

    The process from enrollment to the completion of screening takes about one week.

  • participants' basic information

    basic information from participants, including age, sex, height, weight, BMI, and medical history.

    The process from enrollment to the completion of screening takes about one week.

Interventions

not providedDIAGNOSTIC_TEST

Eligibility Criteria

Age9 Years - 14 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)
Sampling MethodProbability Sample
Study Population

adolescents aged 9 to 14 years in primary and secondary schools

You may qualify if:

  • Age 9-14 years old, enrolled in elementary or middle school.
  • Local residents of Nanchang, excluding students from special schools for children with physical or intellectual disabilities.
  • No underlying medical conditions, and able to complete all examinations without difficulty.
  • Willing to participate in the screening and having signed an informed consent form.

You may not qualify if:

  • Severe Medical Conditions: Individuals with severe diseases of the heart, liver, kidneys, endocrine system, or hematopoietic system.
  • Neurological or Psychiatric History: Individuals with a history of neurological or psychiatric disorders.
  • Refusal to Participate: Individuals who are unwilling or refuse to participate in the screening.
  • Severe Osteoporosis: Individuals diagnosed with severe osteoporosis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nanchang University Affiliated Rehabilitation Hospital

Nanchang, Jiangxi, 330003, China

Location

MeSH Terms

Conditions

Scoliosis

Condition Hierarchy (Ancestors)

Spinal CurvaturesSpinal DiseasesBone DiseasesMusculoskeletal Diseases

Central Study Contacts

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
YING Liang

Study Record Dates

First Submitted

January 26, 2025

First Posted

January 31, 2025

Study Start

July 28, 2025

Primary Completion

September 15, 2025

Study Completion

September 28, 2025

Last Updated

May 30, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will share

Locations