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临床试验/ACTRN12619001423101
ACTRN12619001423101终止1 期

Phase 1, dose escalating study to determine maximum safe exercise training intensity early after stroke

The Florey Institute of Neuroscience and Mental Health0 个研究点目标入组 26 人开始时间: 2019年10月15日最近更新:
适应症

试验速览

阶段
1 期
状态
终止
入组人数
26

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
Non-randomised 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

  • 1) ischaemic stroke diagnosis based on MRI/CT or clinical diagnosis, 2) are within 3 weeks post stroke, 3) have no pre-morbid or current restrictions to exercise, 4) are able to transfer from a sitting position to a standing position either independently or with physical assistance, 5) are able to provide informed consent to participate in the study

排除标准

  • 1) hospitalization for myocardial infarction, heart surgery, or congestive heart failure during the preceding 3 months; 2) significant cardiac pathology (arrhythmia, hypertrophic cardiomyopathy, severe aortic stenosis, or pulmonary embolus); 3) significant pulmonary pathology (i.e. severe chronic obstructive pulmonary disease) and 4) musculoskeletal or neurological problems from conditions other than stroke that would limit the ability to exercise (e.g. Parkinson’s Disease, severe osteoarthritis).

研究者

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