Effect of Barcelona School and Schroth for Adolescent Idiopathic Scoliosis.

February 1, 2023 updated by: Eman Mahmoud sherf eldin, Kafrelsheikh University

Effect of Barcelona Scoliosis Physical Therapy Versus International Scoliosis Schroth Therapy in Adolescent Idiopathic Scoliosis

for adolescent idiopathic scoliosis child, investigator will use Barcelona scoliosis physical therapy school and International scoliosis schroth therapy to see which school is better in dealing with scoliosis.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Egypt
    • Kafrelsheikh
      • Kafr Ash Shaykh, Kafrelsheikh, Egypt
        • Recruiting
        • Physical Therapy
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 15 years (CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

scoliosis with angle < 25 participant has Risser sign of П-V participant is not receiving other treatment during study participant not using braces or muscle relaxants

Exclusion Criteria:

scoliosis due to congenital, neuro-muscular, or syndromic etiology, participant who has true leg length discrepancy participant who has cardiac anomalies participant who has kyphosis.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Barcelona scoliosis physical therapy school
procedure for treating scoliosis
Other: Barcelona scoliosis physical therapy school
procedure for treating Adolescent Idiopathic scoliosis
EXPERIMENTAL: International scoliosis schroth therapy
procedure for treating scoliosis
Other: International scoliosis schroth therapy
procedure for treating Adolescent Idiopathic scoliosis

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cobb's Angle
Time Frame: 3 month
to determine angle of scoliosis
3 month
Angle Trunk Rotation (ATR):
Time Frame: 3 month
to determine amount of hump
3 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
SRS-22 patient questionnaire
Time Frame: 3 month
questionnaire to evaluate pain for spinal deformity patient
3 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Kafrelsheikh University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ANTICIPATED)

February 1, 2023

Primary Completion (ANTICIPATED)

May 1, 2023

Study Completion (ANTICIPATED)

May 30, 2023

Study Registration Dates

First Submitted

December 23, 2022

First Submitted That Met QC Criteria

February 1, 2023

First Posted (ACTUAL)

February 13, 2023

Study Record Updates

Last Update Posted (ACTUAL)

February 13, 2023

Last Update Submitted That Met QC Criteria

February 1, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • EG,KFS lab research

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

share the result of the study not any personal information about patient

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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