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The Effect of Core Exercises in Postoperative Scoliosis

2026年6月3日 更新者:Feride FEHİM、Hasan Kalyoncu University

The Effect of Core Stabilization Exercises on Scapular and Shoulder Asymmetry in Postoperative Adolescent Idiopathic Scoliosis.

This study aims to investigate the effects of a core stabilization-based rehabilitation program following adolescent idiopathic scoliosis (AIS) surgery on radiological parameters, pain, upper extremity function, range of motion, and scapular assessment. Participants diagnosed with AIS and treated with posterior spinal fusion surgery will undergo a rehabilitation program based on core stabilization exercises. Outcome measures will include Cobb angle, vertebral rotation, Visual Analog Scale (VAS), QuickDASH, Trunk Appearance Perception Scale (TAPS), SRS-22, cervical and shoulder range of motion, and scapular assessment tests. Assessments will be conducted before and after the rehabilitation program.

研究概览

详细说明

This study is designed to investigate the effects of a core stabilization-based rehabilitation program following adolescent idiopathic scoliosis (AIS) surgery on radiological, functional, and scapular parameters. Individuals diagnosed with AIS and treated with posterior spinal fusion surgery will be recruited for participation.

Radiological assessment will include thoracic and lumbar Cobb angles and vertebral rotation measurements. Clinical assessments will include the Visual Analog Scale (VAS) for pain, QuickDASH for upper extremity function, Trunk Appearance Perception Scale (TAPS) for body image perception, and SRS-22 for health-related quality of life. Cervical and shoulder range of motion will also be evaluated.

Scapular assessment will include the Lateral Scapular Slide Test (LSST), Scapular Assistance Test (SAT), and wall push-up test. The study aims to evaluate changes in scapular asymmetry, scapular control, and scapulothoracic mechanics following the rehabilitation program.

Assessments will be performed before and after the intervention to examine potential changes in radiological, functional, and scapular outcomes.

研究类型

介入性

注册 (实际的)

20

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  • Individuals diagnosed with adolescent idiopathic scoliosis (AIS)
  • Individuals who underwent posterior spinal fusion surgery
  • Age between 10 and 18 years
  • Individuals participating in a core stabilization-based rehabilitation program
  • Individuals who agreed to participate voluntarily

Exclusion Criteria:

  • Presence of neurological, rheumatological, or other orthopedic disorders affecting posture or upper extremity function
  • History of additional spinal surgery
  • Cognitive impairment preventing participation in evaluations
  • Incomplete assessment data
  • Noncompliance with the rehabilitation program

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Core Stabilization Rehabilitation Group
Participants received a core stabilization-based rehabilitation program after adolescent idiopathic scoliosis surgery. The program included core stabilization, postural control, and scapular stabilization exercises
Participants received a core stabilization-based rehabilitation program following adolescent idiopathic scoliosis surgery. The rehabilitation program included core stabilization exercises, postural control training, scapular stabilization exercises, and functional exercise approaches.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Scapular Assessment
大体时间:10 weeks
Scapular control and asymmetry were evaluated using the Lateral Scapular Slide Test (LSST), Scapular Assistance Test (SAT), and wall push-up test. LSST measures scapular asymmetry by assessing the distance between the scapula and spinal landmarks at different arm positions. Greater side-to-side differences indicate increased scapular asymmetry. SAT evaluates improvement in symptoms and scapular motion during assisted scapular upward rotation. The wall push-up test was used to assess scapular winging and scapular stability.
10 weeks

次要结果测量

结果测量
措施说明
大体时间
Visual Analog Scale (VAS)
大体时间:10 weeks
Pain intensity was evaluated using the Visual Analog Scale (VAS). The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Lower scores indicate reduced pain intensity.
10 weeks

其他结果措施

结果测量
措施说明
大体时间
QuickDASH Score
大体时间:10 weeks
Upper extremity function was assessed using the QuickDASH questionnaire. Scores range from 0 to 100, with higher scores indicating greater disability and poorer upper extremity function. Lower scores indicate functional improvement.
10 weeks
TAPS Score
大体时间:10 weeks
Body image perception was evaluated using the Trunk Appearance Perception Scale (TAPS). Scores range from 1 to 5, with higher scores indicating better perception of trunk appearance and lower deformity perception.
10 weeks
SRS-22 Quality of Life Score
大体时间:10 weeks
Quality of life was assessed using the Scoliosis Research Society-22 questionnaire (SRS-22). The questionnaire evaluates pain, self-image, function, mental health, and satisfaction. Higher scores indicate better quality of life.
10 weeks
Range of Motion
大体时间:10 weeks
Cervical and shoulder range of motion measurements were evaluated using goniometric assessment. Higher values indicate greater joint mobility and flexibility.
10 weeks
Radiological Parameters
大体时间:10 weeks
Vertebral rotation measurements were evaluated radiologically. Lower rotation values indicate reduced spinal deformity.
10 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Yavuz Yakut, Prof. Dr.、Hasan Kalyoncu University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年5月28日

初级完成 (实际的)

2026年4月30日

研究完成 (实际的)

2026年4月30日

研究注册日期

首次提交

2026年5月26日

首先提交符合 QC 标准的

2026年6月3日

首次发布 (实际的)

2026年6月8日

研究记录更新

最后更新发布 (实际的)

2026年6月8日

上次提交的符合 QC 标准的更新

2026年6月3日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • HasanKU-FTR-FF-01

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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