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NCT05227638 Clinical Trial

Investigation of the Efficacy of PNF and Schroth Treatment

Scoliosis; Adolescence Clinical Trial

Official title:
Investigation of the Efficacy of PNF and Schroth Treatment in Adolescent Idiopathic Scoliosis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05227638
Other study ID # E-10879717-050.01.04-2542
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 10, 2021
Est. completion date June 25, 2022

Study information
Verified date August 2023
Source Kirsehir Ahi Evran Universitesi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

our study was to compare the advantages of Schroth and PNF methods used in AIS treatment

Description:

there are studies showing that Schroth and PNF are effective on AIS seperately. While there are studies showing that Schroth is particularly effective on AIS, the number of studies on PNF is insufficient. However, no evidence was found comparing the efficacy of Schroth and PNF. Therefore, the aim of our study was to compare the advantages of Schroth and PNF methods used in AIS treatment

Recruitment information / eligibility
Status Completed
Enrollment 36
Est. completion date June 25, 2022
Est. primary completion date January 22, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 10 Years to 18 Years
Eligibility Inclusion Criteria: - Participants were between ages 10-18 - Volunteered for the study. - Diagnosed with adolescent idiopathic scoliosis - Cobb angle between 10-30 degrees - 0-3 Risser sign - Lenke curve type 1 Exclusion Criteria: - non-idiopathic scoliosis - previous spinal surgery - who had exercise contraindications who had rheumatological disease who had mental handicap and who another neuromuscular problem

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• exercise
participants were between ages 10-18, volunteered for the study, were diagnosed with adolescent idiopathic scoliosis, were Cobb angle between 10-30 degrees, were 0-3 Risser sign, and were Lenke curve type 1.

Locations
Country Name City State
Turkey Mehmet Hanifi KAYA Kirsehir

Sponsors (2)
Lead Sponsor Collaborator
Mehmet Hanifi Kaya Kirsehir Ahi Evran Universitesi

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cobb angle anteroposterior x-ray was taken with the entire spine of the patients standing 8 week
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