UCD School of Medicine, University College Dublin, Dublin 4, Ireland.
HRB Trials Methodology Research Network, NUI Galway, Galway, Ireland.
Trials. 2020 Nov 23;21(1):962. doi: 10.1186/s13063-020-04893-z.
In common with many countries, Ireland has seen an increasing trend in the number of clinical trials conducted over the past few years. Yet, as elsewhere, trialists in Ireland face several problems and barriers in the starting-up of clinical trials. These barriers impede trial activity significantly, with consequent impacts on patient care. It is critical to understand these issues, to develop approaches to facilitate trial start up. This study identifies the challenges in conducting clinical trials in Ireland and specifically the contractual, ethical, logistical, and regulatory barriers that hinder the start-up of investigator-led trials in Ireland.
Data for this study were collected in two stages. In the first stage, a survey was conducted among trialists in Ireland. A total of 44 trialists responded to the survey, and information was collected about their experience in conducting clinical trials, the scale and nature of their most recently completed trial, and the details of specific barriers they encountered during the starting-up of the trial. In the second stage, nine semi-structured interviews were conducted with the awardees of 2018 Irish Health Research Board's Definitive Intervention Feasibility Award. These interviews facilitated a deeper exploration of issues and problems in conducting clinical trials in Ireland.
This study identified several issues and bottlenecks in starting-up clinical trials in Ireland with contracts and ethical approval cited as the major issues. The data shows that site identification and activation was also problematic in some cases. Several respondents reported difficulties in accessing dedicated time for protocol development and believe that support in this area can be greatly beneficial. It was reported that availability of skilled staff members like statisticians and data managers was as an issue, especially for small trials.
This study found that several factors impact trial initiation and progression in Ireland. Delays associated with obtaining contract and ethics approval are perceived as major barriers. Specialist supports in areas such as ethics and regulatory affairs and availability of specialised staff members in areas such as statistics and data management are key actions to enable enhanced clinical trial activity in Ireland.
与许多国家一样,爱尔兰近年来开展的临床试验数量呈上升趋势。然而,与其他国家一样,爱尔兰的试验人员在启动临床试验时面临着一些问题和障碍。这些障碍严重阻碍了试验活动,对患者护理产生了相应的影响。了解这些问题对于制定促进试验启动的方法至关重要。本研究确定了在爱尔兰开展临床试验所面临的挑战,特别是那些阻碍爱尔兰研究者主导试验启动的合同、伦理、后勤和监管方面的障碍。
本研究分两个阶段收集数据。在第一阶段,对爱尔兰的试验人员进行了调查。共有 44 名试验人员对调查做出了回应,收集了他们在开展临床试验方面的经验、他们最近完成的试验的规模和性质,以及在试验启动过程中遇到的具体障碍的详细信息。在第二阶段,对 2018 年爱尔兰健康研究委员会明确干预可行性奖的获得者进行了 9 次半结构化访谈。这些访谈促进了对在爱尔兰开展临床试验的问题和挑战的深入探讨。
本研究确定了在爱尔兰启动临床试验的几个问题和瓶颈,合同和伦理批准被认为是主要问题。数据显示,在某些情况下,确定和激活试验地点也存在问题。一些受访者报告说,在为方案制定分配专门时间方面存在困难,并认为在这方面的支持将非常有益。报告称,像统计学家和数据管理员这样的熟练工作人员的可用性是一个问题,尤其是对于小型试验。
本研究发现,有几个因素影响了爱尔兰的试验启动和进展。获得合同和伦理批准方面的延迟被认为是主要障碍。在伦理和法规事务等领域提供专业支持,以及在统计和数据管理等领域提供专门工作人员的可用性,是在爱尔兰开展更多临床试验的关键措施。