Sensitivity of an Upper Limb Motion Analysis Protocol to Changes in Kinematics and Muscle Activity After Constraint Induced Therapy in Children With Hemiplegia (MouvsupTCIHemi)
2026年9月10日 更新者:Nantes University Hospital
Quantified Analysis of the Movements of the Upper Limb of Children With Hemiparesis Participating in the Stress Induced Therapy Program
In France, Cerebral Palsy (CP) affects 1 in 450 births.
It results from lesions of the brain, before, during, or shortly after birth.
These non-progressive lesions cause muscle impairments, responsible for activity limitations.
These muscle impairments include muscle stiffness, and muscle weakness.
Children with Unilateral CP (UCP) have these impairments on only one side of the body.
To compensate for activity limitations with their impaired arm, these children over-use their non-impaired arm.
The objective of constraint-induced therapy (CIT) is to minimize this asymmetry which deteriorates mobility on the impaired side, by forcing the child to only use its impaired arm several hours a day during several weeks of therapy.
It is known using clinical tests that this therapy improves the overall motor function of the impaired arm.
However, the underlying mechanisms are yet unknown.
An understanding of these mechanisms would suggest ways to maximize the effectiveness of this therapy, which requires a significant commitment from the child and its family.
The investigaors propose in this project a quantitative and objective evaluation of the effect of CIT on the movements of the impaired arm of children with UCP.
The investogators focus their analysis on muscle activation, to assess which aspect of muscle impairments is modified by CIT.
To this end, the investigators will use sensors identical to those already used in clinics for the Quantified Gait Analysis of children with CP, recognized since 2006 by the Haute Autorité de Santé as providing key supplementary data in the evaluation of complex gait disorders.
Results from this study will provide leads to optimize CIT.
Some children could for example benefit from CIT paired with treatments to reduce muscle stiffness or to strengthen muscles
研究概览
地位
完全的
条件
详细说明
Quantitative and objective evaluation of upper limb movements will take place in a motion analysis laboratory and will take place as follow:
- A clinical exam of the participant will be performed by the physician to collect maximal passive joint amplitudes with a goniometer and anatomical measures (length, circumference) of the upper limb.
- The participant will be equipped with surface electromyographic electrodes to measure the activation of his superficial muscles, and with retroreflective markers placed on anatomical landmarks of his thorax, shoulder, and arm, to measure upper limb kinematics with a 3D motion capture system composed of 8 VICON cameras.
- Maximal forces of elbow pronosupination and flexion-extension will be measured with a portable dynamometer.
The participant will be placed on a height adjustable bench, in the center of the laboratory. He will be asked to perform upper limb movements:
- A few movements not measured, to familiarize with the equipment;
- Recorded movements: a trial is composed of a few consecutive cycles of a movement such as elbow flexion-extension. A trial usually last about 10seconds. A few seconds-time of rest is imposed between each trial. The required movements are the following: elbow flexion-extension, elbow pronosupination, and "hand to mouth".
- Finally, the participant will be asked to lie down on an exam table and to rest relax, in order to measure the electromyographic signal of his muscles at rest.
Duration of the protocol is about 1h30, with less than 30seconds of effort, and a few minutes of performing simple upper limb movements.
研究类型
介入性
注册 (实际的)
28
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
-
-
-
Nantes、法国、46208
- CHU de Nantes
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-
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
6年 至 17年 (孩子)
接受健康志愿者
是的
描述
Inclusion Criteria:
- Participants (excluding healthy volunteers) must have hemiparesis.
- Children must be between 6 and 17 years of age. The protocol requires a minimum concentration difficult to obtain for children under 6 years.
- Participants must be enrolled in a health insurance plan.
Exclusion Criteria:
- Inability to understand or follow instructions during 1h30.
- Physical incapacity to carry out the requested movements
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:其他
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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其他:A: Healthy volunteers
|
Maximal forces of elbow pronosupination and flexion-extension will be measured with a portable dynamometer.
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其他:B: Patient with heamiplegia
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Maximal forces of elbow pronosupination and flexion-extension will be measured with a portable dynamometer.
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其他:C: Patient with heamiplegia and constraint induced therapy
arm with constraint induced therapy (done before the protocol)
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Maximal forces of elbow pronosupination and flexion-extension will be measured with a portable dynamometer.
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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 |
|---|---|---|
|
Upper limb muscle activation envelopes
大体时间:5 weeks
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Muscle activation envelopes come from electromyographic signals of upper limb muscles.
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5 weeks
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kinematics during active movements
大体时间:5 weeks
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Kinematics: angles, velocities, accelerations of the thorax, shoulder, elbow and wrist in the three anatomical plans (sagittal, frontal, transverse).
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5 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。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
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)
2017年3月28日
初级完成 (实际的)
2019年4月17日
研究完成 (实际的)
2019年4月17日
研究注册日期
首次提交
2017年3月20日
首先提交符合 QC 标准的
2017年3月28日
首次发布 (实际的)
2017年4月4日
研究记录更新
最后更新发布 (实际的)
2026年9月14日
上次提交的符合 QC 标准的更新
2026年9月10日
最后验证
2019年6月1日
更多信息
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