Effect of Barcelona School and Schroth for Adolescent Idiopathic Scoliosis.

• Sponsor: Kafrelsheikh University (Other)
• Overall Status: Recruiting
• CT.gov ID: NCT05723952
• Collaborator: (none)
• Enrollment: 30
• Location: 1
• Arms: 2
• Anticipated Duration (Months): 3.9
• Patients Per Site Per Month: 7.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Adolescent Idiopathic Scoliosis, Thoracic Region	Other: Barcelona scoliosis physical therapy school; Other: International scoliosis schroth therapy	N/A

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 30 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Participant)
• Primary Purpose: Treatment
• Official Title: Effect of Barcelona Scoliosis Physical Therapy Versus International Scoliosis Schroth Therapy in Adolescent Idiopathic Scoliosis
• Anticipated Study Start Date: Feb 1, 2023
• Anticipated Primary Completion Date: May 1, 2023
• Anticipated Study Completion Date: May 30, 2023

Arms and Interventions

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

Outcome Measures

Primary Outcome Measures

1. Cobb's Angle [3 month]

   to determine angle of scoliosis

2. Angle Trunk Rotation (ATR): [3 month]

   to determine amount of hump

Secondary Outcome Measures

1. SRS-22 patient questionnaire [3 month]

   questionnaire to evaluate pain for spinal deformity patient

Eligibility Criteria

Criteria

• Ages Eligible for Study: 12 Years to 15 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

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.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Physical Therapy	Kafr Ash Shaykh	Kafrelsheikh	Egypt

Sponsors and Collaborators

• Kafrelsheikh University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Eman Mahmoud sherf eldin, master student, Kafrelsheikh University
• ClinicalTrials.gov Identifier: NCT05723952
• Other Study ID Numbers: EG,KFS lab research
• First Posted: Feb 13, 2023
• Last Update Posted: Feb 13, 2023
• Last Verified: Feb 1, 2023

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Scoliosis

Study Results

No Results Posted as of Feb 13, 2023