NCT07639632尚未招募不适用
Reduce Inefficiencies in Management of Spasticity
The University of Texas Health Science Center, Houston1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年6月15日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
研究概览
简要总结
The purpose of this study is to evaluate the effectiveness of a spasticity screener and to determine if the spasticity screener results are useful to healthcare providers and impact clinical decision making
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Currently admitted for an acute hemorrhagic or ischemic stroke; recurrent stroke allowed if no spasticity at baseline
- •NIHSS score of > 0 on items 5 or 6 (required of at least 1 limb)
- •Willingness to participate in the study for 24 months
- •Able to sign consent form or availability of a legally authorized representative to sign
- •Able to read/write in English
- •Identified MD for follow up post hospitalization
排除标准
- •Botulinum toxin use for any indication within the past 12 weeks
- •Acute life threatening illness
- •Prior limb injury or neurological diagnosis that limited movement in the now affected limb(s)
- •Any terminal illness that would limit participation in study follow ups
- •Known spasticity or other movement disorders that impact tone
研究组 & 干预措施
Standard of care
Active Comparator
干预措施: Standard of care (Other)
Screener
Experimental
干预措施: Screener (Other)
研究者
Sean Savitz
Professor
The University of Texas Health Science Center, Houston
研究点 (1)
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