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首页> 外文期刊>Journal of neurotrauma >Facilitators and Barriers to Spinal Cord Injury Clinical Trial Participation: Multi-National Perspective of People Living with Spinal Cord Injury
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Facilitators and Barriers to Spinal Cord Injury Clinical Trial Participation: Multi-National Perspective of People Living with Spinal Cord Injury

机译:脊髓损伤临床试验参与的促进因素和障碍:脊髓损伤患者的多民族视角

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摘要

These are exciting times for the translation of promising interventions for spinal cord injury (SCI) into testing with clinical trials. These interventions include acute surgical decompression, neuroprotection, neural repair, cell replacement, activity-based rehabilitation, and medical devices, including devices requiring surgical implantation. By nature, clinical trials can have strict inclusion and exclusion criteria, which narrow down the pool of potential participants. Meeting enrollment numbers for properly powered trials is a daunting task. Therefore, it is important that trials are designed in a manner that facilitates participation. The purpose of this research study was to learn more about the factors that encourage or interfere with the decision to participate in clinical trials from the perspective of people living with SCI. A multi-national survey was conducted, primarily online, in which 802 participants with SCI ranked 32 factors as facilitators or barriers, using a Likert-type scale. There were 13 universal facilitators, five universal barriers, and three universally neutral factors. The number one facilitator was possible improvement in functionality and the number one barrier was possible decline in functionality-as may be expected. However, many unexpected facilitators and barriers were identified. There also were certain factors that were strong barriers or facilitators to certain sub-groups of people living with SCI. All of these factors should be taken into careful consideration when designing clinical trials so as to promote enrollment and enable adherence to different protocols.
机译:现在是将令人振奋的脊髓损伤(SCI)干预措施转化为临床试验测试的激动人心的时刻。这些干预措施包括急性手术减压,神经保护,神经修复,细胞置换,基于活动的康复和医疗器械,包括需要手术植入的器械。从本质上讲,临床试验可以具有严格的纳入和排除标准,从而缩小了潜在参与者的范围。满足注册人数以进行正确的试验是一项艰巨的任务。因此,以有助于参与的方式设计试验很重要。这项研究的目的是从患有SCI的人的角度了解更多有关鼓励或干扰参与临床试验决定的因素。进行了一项多国调查,主要是在线进行的,其中,使用李克特型量表,有SCI的802名参与者将32个因素作为促进因素或障碍进行了排名。有13个普遍推动者,5个普遍障碍和3个普遍中立因素。如预期的那样,第一促进者是功能方面的可能改进,而第一障碍是功能方面的可能降低。但是,发现了许多意外的促进因素和障碍。也有某些因素成为SCI某些亚人群的强大障碍或促进者。在设计临床试验时,应仔细考虑所有这些因素,以促进入组并遵循不同的方案。

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