跳至主要内容
临床试验/NCT03479632
NCT03479632Unknown不适用

Aerobic Walking Exercise for Non-Ambulatory Stroke Survivors

University of Kansas Medical Center2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年3月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
40
试验地点
2
主要终点
Resting Heart Rate

研究概览

简要总结

By doing this study, researchers hope to learn the effects of aerobic exercise on heart, lung, and bone health in people who cannot walk after a stroke.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Independent ambulation before stroke
  • Be able to understand and follow verbal commands in English
  • Have physicians' approval for exercise, and be in stable medical condition
  • Participant's first stroke
  • Unable to walk independently according to Functional Ambulation Category (FAC) (<2) after in-patient rehabilitation treatment
  • Between 6 weeks to 5 years after stroke onset

排除标准

  • Current cardiovascular abnormalities other than stroke such as ischemic cardiovascular event or coronary artery bypass surgery less than 3 months ago
  • Musculoskeletal disorder which prevents subjects from participating in the exercise
  • Resting blood pressure more than 200/110 mm Hg
  • Current or previous pulmonary diseases in the past two years
  • Osteoporosis and restricted passive movement in the major joints of the lower limbs
  • Subjects will be excluded if they are unable to speak or understand English and/or unable to travel to the University of Kansas Medical Center (KUMC) Neuromuscular Research Laboratory

研究组 & 干预措施

Intervention Group

Experimental

The intervention group will undergo an aerobic walking program using a treadmill, a body-weight support system, and an assistive device.

干预措施: Aerobic walking program (Behavioral)

Control Group

Active Comparator

The control group will receive standard physical therapy (PT).

干预措施: Standard physical therapy (Behavioral)

结局指标

主要结局

Resting Heart Rate

时间窗: Change from Baseline to Week 8

次要结局

  • Change in vital capacity (VC)(Change from Baseline to Week 8)
  • Resting blood pressure(Change from Baseline to Week 8)
  • Change in forced vital capacity (FVC)(Change from Baseline to Week 8)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验