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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05298371
Other study ID # B Akcay
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 3, 2022
Est. completion date June 15, 2022

Study information

Verified date October 2023
Source Bandirma Onyedi Eylül University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The aim of this study is to investigate the acute effect of activities of daily living on trunk rotation in patients with adolescent idiopathic scoliosis.


Description:

Patients with AIS who applied to Bandırma Onyedi Eylül University Physiotherapy and Rehabilitation Department will be included in this study. Individuals diagnosed with AIS, whose Cobb angle is between 20º -50º, who do not have any chronic diseases that require neurological or psychiatric medication, and who volunteer to participate in the study will be included. Individuals with any contraindications for exercise, previous spine surgery, thoracic apex curvature of 6 or more, mental problems, non-idiopathic scoliosis but with different causes will be excluded from the study. To determine the demographic characteristics of the participants, age, gender, weight, height, presence of chronic disease, age at first diagnosis, exercise habits, treatments, and brace use will be questioned. The ATR will be used to measure degrees of trunk rotation to monitor the effects of treatment without radiographic evaluation. On the first day, the demographic characteristics of the participants will be questioned, Cobb angles, Risser findings, and ATR degrees will be recorded. After the first day, all postural activities and measurements will be taken on different days (at least three days apart) not to affect the degrees of trunk rotation in patients with AIS.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date June 15, 2022
Est. primary completion date May 15, 2022
Accepts healthy volunteers No
Gender All
Age group 10 Years to 35 Years
Eligibility Inclusion Criteria: - Being diagnosed with AIS between the ages of 10-35 - Cobb angle between 20º -50º, - To be able to continue the program to be applied, - Not having a chronic disease that requires the use of any neurological or psychiatric medication, - The willingness of parents and/or patients to participate in the study. Exclusion Criteria: - The patient has any contraindications for exercise, - Having had previous spine surgery, - Having a curvature of 6 or more thoracic apex, - Having any mental problems, - The fact that scoliosis is not idiopathic but has arisen for different reasons (neurological, congenital, etc.)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Corrected Sitting postures
Change after being in Corrected Sitting postures
Natural / relaxed sitting postures
Change after being in relaxed sitting postures
Corrected Standing posture
Change after being in Corrected Standing posture
Natural / relaxed standing postures
Change after being in relaxed standing postures

Locations

Country Name City State
Turkey Burçin Akçay Balikesir

Sponsors (1)

Lead Sponsor Collaborator
Burçin Akçay

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Angle of trunk rotation (ATR) ATR can be used to monitor the effects of treatment without radiographic evaluation. ATR measurement is done using a special inclinometer called a scoliometer. The patient is asked to lean forward with the arms relaxed. The scoliometer is placed posteriorly and the degree observed at the point of greatest gimbosity is recorded. Change from Baseline angle of trunk rotation at 5 minutes
Primary Demographic Characteristics Within the scope of the demographic information form, participants' age, gender, weight, height, presence of chronic diseases, age at which they were first diagnosed, exercise habits, treatments received, brace use will be questioned. Baseline
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