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临床试验/NCT06128746
NCT06128746招募中不适用

Repetitive Transcranial Magnetic Stimulation (rTMS) for the Treatment of Spasticity in Children With Hemiplegic Cerebral Palsy/ Hemiplegia Due to Acquired Brain Injury - a Randomized Controlled Trial

The University of Hong Kong2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年1月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
2
主要终点
The range of motion scores

研究概览

简要总结

This RCT aims to investigate the effect of repetitive transcranial magnatic stimulation (rTMS) in treating children with hemiplegoc cerebral palsy. The study will measure any improvement in spasticity after using contra-lesional inhibitory rTMS follow by intensive limb training.

Participants will attend a 10-day rTMS treatment sessions, follow by intensive training of the impaired limb. They will also undergo MRI scans before and after the treatment to investiagte the underlying neurophysiological mechanisms that lead to changes clinically by using TMS as well as MR-DKI. Researchers will compare the intervention group and the sham group to see if rTMS could result in improvement of participants' spasticity.

详细描述

Cerebral palsy is the most common cause of lifelong physical disability in childhood, with an estimated prevalence of 1.5 per 1000 living biths for primary school-aged children. Spasticity is the most common symptoms in children with cerebral palsy, leading to muscle weakness affecting gross motor functions and causing complications such as pain, contracture and subluzation which will lead to inability to perform activity-based training and subsequently lead to further muscle weakness. Standard therapy with regular physiotherapy and occupational therapy are essential but time-consuming and the effects might not last for longer duration. Patients or caregivers decline medications because of side effects drowsiness while other interventions such as intra-thecal baclofen pump, rhizotomy or surgery are invasive.

Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive brain stimulation technique that has the ability to modulate excitation of the motor cortex area of the brain. There were past studies suggesting that using contralesional inhibitory rTMS was safe and feasible for patients with paediatric subcortical stroke and seemed to improve hand function in patients with hemiparesis. However, limited studies have been published on the effects of rTMS on improving spasticity in children with cerebral palsy. Hence, the objective of this study is to use low-frequency rTMS to the contra-lesional hemisphere in children with hemiplegic cerebral palsy to investigate if rTMS follow by intensive limb training would improve spasiticity of these children and whether the improvement can be sustained for a longer time. The underlying mechanisms that lead to the changes clinically will also be investigated by TMS and MRI.

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
7 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged between 7 years and 18 years
  • Diagnosis of cerebral palsy with hemiplegia
  • Upper limb spasticity ≥ 1

排除标准

  • Any contra-indications to rTMS
  • Severe spasticity (score of 4 or more in Ashworth scale)
  • Uncontrollable epilepsy
  • History of Botulinum toxin A injection in previous 6 months
  • Upper limb casting in previous 6 months

研究组 & 干预措施

Interventional rTMS group

Experimental

The intervention group will receive 1 Hz active rTMS during treatment, lasting for 20 minutes, follow up by 30 minutes of intensive limb training.

干预措施: Repetitive Transcranial Magnetic Stimulation (Device)

Sham rTMS group

Sham Comparator

The sham group will not receive any Hz of rTMS during treatment, also lasting for 20 minutes with 30 minutes of intensive limb training afterwards.

干预措施: Sham Repetitive Transcranial Magnetic Stimulation (Device)

结局指标

主要结局

The range of motion scores

时间窗: Day 10, 17 of intervention and 2 months post intervention

ROM of thumb adduction, wrist dorsal flexion and extension, and elbow dorsal flexion and extension. Patients' range of motion score will be compared to the normative values

Modified Ashworth Scale

时间窗: Day 10, 17 of intervention and 2 months post intervention

Clinical measure of spasticity. Scores range from 0 to 4, with a higher score indicate worse in muscle tone

次要结局

  • Zancolli scale(Day 10, 17 of intervention and 2 months post intervention)
  • Gross motor function measure(Day 10, 17 of intervention and 2 months post intervention)
  • Pediatric Quality of Life Cerebral Palsy module(Day 10, 17 of intervention and 2 months post intervention)
  • MRI Brain: fMRI and DKI(Day 10, 17 of intervention and 2 months post intervention)
  • Assisting hand assessment(Day 10, 17 of intervention and 2 months post intervention)
  • House functional classification scale(Day 10, 17 of intervention and 2 months post intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Winnie Wan Yee Tso (Dr)

Clinical Assistant Professor

The University of Hong Kong

研究点 (2)

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