The Effect of Exercise on Paravertebral Muscle Thickness and Quality of Life in Adolescent Idiopathic Scoliosis

NCT ID: NCT07250295

Last Updated: 2026-01-09

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

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-01

Study Completion Date

2022-08-15

Brief Summary

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The study population comprised patients with AIS who had applied to the outpatient clinic between January and June 2022. The patients were divided into two groups. Treatment group(TG) was instructed in specific scoliosis exercises, while the Control group(CG) was given exercises for the lower extremities. Each patient was included in a 12- week exercise program accompanied by a physiotherapist. The patients' quality of life, and paravertebral muscles were evaluated ultrasonographically before and after treatment.

Detailed Description

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Conditions

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Adolescent Idiopathic Scoliosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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Treatment Group

The treatment group (TG) was given exercises for the thoracic and lumbar regions for scoliosis.

Group Type ACTIVE_COMPARATOR

Exercise

Intervention Type OTHER

Patients were expected to attend treatment under the supervision of a physiotherapist. If they missed a day, they were contacted by phone and advised to do their exercises at home. The number of days they missed did not exceed five. Each set included a 30-second rest period to prevent fatigue. A five-minute warm-up and cool-down period was allotted before and after the exercise session. The exercise program was implemented by a physiotherapist with three years of experience in scoliosis management. Before initiating the intervention, the physiotherapist underwent a structured training session, including practical demonstrations, supervised practice, and detailed exercise protocols.

Control Group

The control group (CG) was instructed to perform gluteus maximus, hamstring, and quadriceps strengthening exercises.

Group Type PLACEBO_COMPARATOR

Exercise for Lower Extremities

Intervention Type OTHER

The control group (CG) was instructed to perform gluteus maximus, hamstring, and quadriceps strengthening exercises.

Interventions

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Exercise

Patients were expected to attend treatment under the supervision of a physiotherapist. If they missed a day, they were contacted by phone and advised to do their exercises at home. The number of days they missed did not exceed five. Each set included a 30-second rest period to prevent fatigue. A five-minute warm-up and cool-down period was allotted before and after the exercise session. The exercise program was implemented by a physiotherapist with three years of experience in scoliosis management. Before initiating the intervention, the physiotherapist underwent a structured training session, including practical demonstrations, supervised practice, and detailed exercise protocols.

Intervention Type OTHER

Exercise for Lower Extremities

The control group (CG) was instructed to perform gluteus maximus, hamstring, and quadriceps strengthening exercises.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients who had been diagnosed with AIS by means of radiographic and clinical examination of the spine were included in the study.

Exclusion Criteria

* Cases with a history of surgery to the paravertebral region
* Metabolic bone disease
* Neuromuscular disease
* chromosomal anomaly
* Serious autoimmune and endocrine disease
* Congenital scoliosis
* Skeletal dysplasia and serious cognitive impairment
Minimum Eligible Age

10 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sisli Hamidiye Etfal Training and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Roza Jizel Dagdelen MD

MD, Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hamidiye Etfal Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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28.12.2021 / 3388

Identifier Type: -

Identifier Source: org_study_id

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