ACTRN12623000255684尚未招募未知
A reliability study in Inclusion Body Myositis (IBM) to evaluate knee extensor strength using a stabilisation strap
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Age at least 18 years or over
- •Has a confirmed diagnosis of Inclusion Body Myositis by a neuromuscular specialist
- •Able to attend the a single study visit of approximately 3 hours duration during the study period
- •Able to provide written informed consent for the study
- •Able to independently and safely transfer on and off the Humac Norm
- •Knee extensor modified Medical Research Council grade of at least 4- in one or both legs as assessed within the past 6 months.
排除标准
- •Recent history (within six months) of fracture or pathology affecting the knee joint that would reasonably cause pain or discomfort or prevent the participant from performing a resisted knee extension.
- •Any condition precluding the participant from performing any part of the study procedures.
- •Any clinical assessment by the Sponsor-Investigator that the participant is unable or unsafe to take part in the study.
研究者
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