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临床试验/NCT06730269
NCT06730269已完成不适用

Comparative Efficacy of Face-to-Face and Telerehabilitation Approaches in Managing Thoracic Hyperkyphosis Among 9-12-Year-Olds: a Randomized Clinical Trial

Medipol University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
1
主要终点
Thoracic Kyphosis Angle (TKA)

研究概览

简要总结

This study evaluates the effectiveness of face-to-face versus telerehabilitation programs for children aged 9-12 with thoracic hyperkyphosis, a condition caused by poor posture that leads to excessive forward curvature of the spine. Twenty children participated in a six-week corrective exercise program, either in person or through an online platform. Both approaches significantly improved spinal posture, back muscle strength, and pain levels, with no notable differences in outcomes between the two methods. The findings suggest that telerehabilitation is as effective as face-to-face rehabilitation, offering a flexible option for managing thoracic hyperkyphosis in children.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
9 Years 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged 9-12 years.
  • Diagnosed with thoracic hyperkyphosis (Thoracic Kyphosis Angle > 40 degrees).
  • Able to participate in a 6-week rehabilitation program (face-to-face or telerehabilitation).

排除标准

  • Children with congenital spinal malformations.
  • Children with mental health issues that could interfere with participation or compliance in the study.

结局指标

主要结局

Thoracic Kyphosis Angle (TKA)

时间窗: 6 weeks

It was measured using a flexicurve ruler to assess the curvature of the thoracic spine before and after the intervention. \>45° is considered hyperkyphosis

Manual Muscle Test (MMT)

时间窗: 6 weeks

Evaluates back muscle strength before and after the intervention. Minimum = 0 (no muscle contraction), Maximum = 5 (normal muscle strength).

Visual Analog Scale (VAS)

时间窗: 6 weeks

Assesses pain levels before and after the intervention. Minimum = 0 (no pain), Maximum = 10 (worst possible pain)

次要结局

未报告次要终点

研究者

发起方
Medipol University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Seda GÖZENER CANBÜLBÜL

PhD candidate

Medipol University

研究点 (1)

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