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临床试验/NCT06907381
NCT06907381已完成不适用

Blood Flow-restricted Resistance Exercise to Promote Muscle Strength and Use in Adults With Incomplete Spinal Cord Injury

Quality Living, Inc.1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2025年4月1日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
Change in muscle strength

研究概览

简要总结

Recovery of arm and hand motor control is critical for independence and quality of life following incomplete spinal cord injury (iSCI). Blood flow-restricted resistance exercise (BFRE) has emerged as a potential treatment addressing this need, but treatment guidelines and research reporting effectiveness are sparse. The purpose of this work is to provide case reports of people with cervical iSCI who use BFRE supplemented by electrical stimulation (ES) to increase the strength and functional use of selected upper extremity muscles.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
19 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Incomplete cervical spinal cord injury
  • Resting blood pressure between 80/50 mmHg and 150/90 mmHg for at least three consecutive days
  • Native speaker of English

排除标准

  • Recent history of deep vein thrombosis or cardiovascular disease including uncontrolled hypertension or a blood-clotting disorder
  • Routine experience of orthostatic hypotension as defined as a drop in systolic/diastolic blood pressure greater than 20/10 mmHg when engaging in physical activity
  • Severe cognitive, communication, or behavioral disorder as determined by treatment team

结局指标

主要结局

Change in muscle strength

时间窗: Baseline and end of treatment at a maximum of 6 months

Change in strength of target muscle(s) contraction as measured in pounds of force using a dynamometer.

次要结局

  • Change in number of repetitions of unassisted target muscle(s) contractions(Baseline and end of treatment at a maximum of 6 months)
  • Change in support required to perform functional task(Baseline and end of treatment at a maximum of 6 months)
  • Change in perceived exertion when performing a functional task(Baseline and end of treatment at a maximum of 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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