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
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