Structured 3D Exercise and the Conventional Exercise Program for Scoliosis in Children With Rheumatic Disease

NCT ID: NCT05377086

Last Updated: 2023-06-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-05-17

Study Completion Date

2023-02-01

Brief Summary

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Usage including cases followed up with rheumatism diagnosis and treatment in Istanbul University-Cerrahpasa Medical Faculty Pediatric Rheumatology Clinic, Physiotherapy and Rehabilitation Unit. The study included 50 patients with a spinal x-ray scoliosis problem, aged 8-16 years, who were diagnosed with rheumatism at least 6 months ago, whose medical treatment was stable, Risser 0-4 and exercise indication (Cobb = 10-45ͦ). Patients with additional neurological diagnosis against rheumatism, who have received any previous treatment for a spine problem, who have a mental state and who do not have the consent of their family will not be included. The cases will be divided into 2 groups by method. In the first group (n = 25), structured 3-dimensional scoliosis exercises are taught in the clinic, and the second group (n = 25) is taught conventional physiotherapy applications (posture-core applications-bennet protocols) in the clinic, and both groups are followed by the WTE method.

Detailed Description

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The demographic and clinical characteristics of all subjects willing to participate in the study will be questioned with the "Sociodemographic Data Form". Sociodemographic data form; pain, age, gender, height, weight, type of rheumatism, how many years ago the patient was diagnosed, the presence of rheumatism and scoliosis in the family, the drugs used, exercise habits, exacerbation history, whether they used a device before, and the awareness of the family about scoliosis. The trunk rotation angles with the forward bend test and the Cobb angle with the SubrotoAngleAid application via x-ray. Respiratory functions will be evaluated with portable spirometer, body awareness will be evaluated with Walter Reed Visual Assessment Scale, and quality of life will be evaluated with Scoliosis Research Association Scale-22 (SRS-22). After the evaluations, in the first treatment session in the clinic, the cases in the first group; Body awareness, respiratory control, differences between rotational and normal breathing, posture exercises and core stabilization exercises will be taught and family training will be provided. In the next session, a home program will be created by applying 3D scoliosis exercises that are structured according to the needs of the patients. Body awareness, respiratory control, posture exercises and core stabilization exercises will be taught and family training will be given to the patients in the second group in the first treatment session. In the next session, conventional exercises for the needs of the cases will be taught and a home exercise program will be created. Both groups will be interviewed for 2-week periods using the WTE method, and the exercises will be progressed gradually as needed. At the beginning of the treatment and in the 6th month, all evaluations will be repeated and the effectiveness of the exercises will be investigated. SPSS (Statistical Package for Social Sciences) (SPSS 21.0) statistical program will be used in the statistical analysis of the data. In all statistical analyzes, p \<0.05 will be considered significant.

Conditions

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Scoliosis Juvenile Idiopathic Arthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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schroth group

This arm was planned as the exercise group which includes Schroth 3-Dimensional scoliosis exercise.

Group Type EXPERIMENTAL

Schroth 3-Dimensional scoliosis exercise

Intervention Type OTHER

Schroth 3-Dimensional scoliosis exercises

conventional group

This arm was planned as the exercise group which includes conventional scoliosis exercise.

Group Type EXPERIMENTAL

conventional scoliosis exercise

Intervention Type OTHER

conventional scoliosis exercise

Interventions

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Schroth 3-Dimensional scoliosis exercise

Schroth 3-Dimensional scoliosis exercises

Intervention Type OTHER

conventional scoliosis exercise

conventional scoliosis exercise

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Cases with a diagnosis of rheumatism in whom scoliosis problems were detected by spine X-ray,
* be between the ages of 8-16,
* Being between 0-4 in the riser,
* Being in exercise indication (Cobb=10-45 ˚)

Exclusion Criteria

* Having an additional neurological or orthopedic diagnosis other than scoliosis accompanying rheumatism and affecting treatment results
* Having had any surgery on the spine
* Have had previous scoliosis treatment poor mental state
Minimum Eligible Age

8 Years

Maximum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Biruni University

OTHER

Sponsor Role lead

Responsible Party

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Eylül Pınar KISA

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Eylül Pınar Kısa

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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PHD Thesis

Identifier Type: -

Identifier Source: org_study_id

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