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临床试验/ACTRN12623001135606
ACTRN12623001135606尚未招募Unknown

Objective measurement of muscle co-contraction pre-and post-Botulinum Toxin-A injection in adults with focal spasticity

A/Prof Ian Baguley0 个研究点目标入组 90 人开始时间: 2023年11月3日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Clinical Group:
  • Ability to understand verbal instructions in English
  • Motor overactivity resulting from an UMN syndrome of greater than 3 months duration
  • Predominately unilateral disability.
  • Presence of active grip strength in the most affected upper limb (a minimum of 0.75kg of force)
  • * People who are receiving Botulinum Toxin-A injections as part of their spasticity management.
  • Control group
  • Age 18+ years
  • Ability to understand verbal instructions in English
  • Available for two assessments

排除标准

  • Other causes of upper limb weakness including non-neurological pain, rheumatological conditions, lower motor neuron lesions, etc.
  • Inadequate ability to understand and follow instructions, such as language barriers or inadequate voluntary motor control.
  • People with spasticity who are not being offered OnabotulinumtoxinA injections as a clinical treatment.
  • * People with a known contraindication to OnabotulinumtoxinA e.g., Eaton-Lambert syndrome, pregnancy, hypersensitivity etc.
  • Control group
  • Self-reported neurological impairment
  • Self-reported acute or chronic arm injury or impairment

研究者

发起方
A/Prof Ian Baguley

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