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Comparative trials on hybrid walking systems for people with paraplegia

机译:对截瘫人民混合行走系统的比较试验

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摘要

A new orthosis (SEPRIX) which combines user friendliness with low energy cost of walking has been developed and will be subject to a clinical comparison with conventional hip-knee-ankle-foot orthoses. In designing such comparative trials it was considered it may be worthwhile to use previous clinical studies as practical examples. A literature search was conducted in order to select all comparative trials which have studied two walking systems (hip-knee-ankle-foot orthoses) for patients with a complete thoracic lesion. Study population, intervention, study design, outcome measurement and statistical analyses were examined. Statistical power was calculated where possible. Of 12 selected studies, 7 were simple A-B comparisons, 2 A-B comparisons with a replication, 2 cross-over trials and 1 non-randomised parallel group design, the last of which was considered internally invalid due to severe confounding by indication. All A-B comparisons were considered internally invalid as well, since they have not taken into account that a comparison of two orthoses requires a control for aspecific effects (like test effects) which may cause a difference. Statistical power could only be examined in 4 studies and the highest statistical power achieved in one study was 47 %. It is concluded that statistical power was too low to be able to detect differences. Even analysis through interval estimation showed that the estimation of the difference was too imprecise to be useful. Since the majority of the surveyed papers have reported small studies (of only 4–6 patients), it is assumed that lack of statistical power is a more general problem. Three possibilities are discussed in order to enhance statistical power in comparative trials, i.e. multicentre studies, statistical pooling of results and improving the efficiency of study design by means of interrupted time series designs.
机译:一种新的矫正器(SEPRIX),其结合了行走的低能量成本的用户友好已经开发并会受到与常规髋膝踝足矫形器的临床对比。在设计这样的比较试验有人认为它可能是值得使用以前的临床研究,作为实际的例子。文献检索是为了选择已经研究了两名病人行走系统(髋膝踝足矫形器)拥有完整的胸椎病变都比较试验进行。研究人群,干预,研究设计,结果测量和统计分析进行了检查。计算在可能的统计力量。 12项选定的研究中,7是简单的A-B比较,与复制2 A-B比较,2交叉试验和1个非随机化平行组设计,其中最后的被指示视为严重混杂内部由于无效。所有A-B比较被认为是无效的内部为好,因为它们没有考虑到两个矫形器的比较需要用于非特异性作用的控制(如测试效果),这可能会导致的差异。只能在4项研究,并在一项研究中达到的最高统计力量进行检查统计功率为47%。它的结论是统计功率太低,能够检测的差异。通过区间估计即使分析结果表明,差的估计太不确切是有用的。由于多数被调查的论文报道的小规模研究(仅4-6个的患者),假定统计力量不足是一个更一般的问题。这三种可能性,以提高在比较试验的统计力量,即多中心研究,结果的统计池和通过的中断时间序列设计来改进研究设计的效率讨论。

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