Clinical Trials Transformation Initiative, Duke University, Durham, NC, USA.
Department of Population Health Sciences, Duke University, 215 Morris Street, Suite 210, Durham, NC, 27701, USA.
Ther Innov Regul Sci. 2021 Mar;55(2):324-335. doi: 10.1007/s43441-020-00217-0. Epub 2020 Sep 29.
Patient group engagement is increasingly used to inform the design, conduct, and dissemination of clinical trials and other medical research activities. However, the priorities of industry sponsors and patient groups differ, and there is currently no framework to help these groups identify mutually beneficial engagement activities.
We conducted 28 qualitative, semi-structured interviews with representatives from research sponsor organizations (n = 14) and patient groups (n = 14) to determine: (1) how representatives define benefits and investments of patient group engagement in medical product development, and (2) to refine a list of 31 predefined patient group engagement activities.
Patient group and sponsor representatives described similar benefits: engagement activities can enhance the quality and efficiency of clinical trials by improving patient recruitment and retention, reduce costs, and help trials meet expectations of regulators and payers. All representatives indicated that investments include both dedicated staff time and expertise, and financial resources. Factors to consider when evaluating benefits and investments were also identified as were suggestions for clarifying the list of engagement activities.
Using these findings, we refined the 31 engagement activities to 24 unique activities across the medical product development lifecycle. We also developed a web-based prioritization tool ( https://prioritizationtool.ctti-clinicaltrials.org/ ) to help clinical research sponsors and patient groups identify high-priority engagement activities. Use of this tool can help sponsors and patient groups identify the engagement activities that they believe will provide the most benefit for the least investment and may lead to more meaningful and mutually beneficial partnerships in medical product development.
患者群体参与越来越多地用于为临床试验和其他医学研究活动的设计、实施和传播提供信息。然而,工业赞助商和患者群体的优先事项不同,目前还没有框架来帮助这些群体确定互利的参与活动。
我们对来自研究赞助商组织(n=14)和患者群体(n=14)的代表进行了 28 次定性、半结构化访谈,以确定:(1)代表们如何定义患者群体参与医疗产品开发的利益和投资,以及(2)细化 31 项预先确定的患者群体参与活动清单。
患者群体和赞助商代表描述了相似的利益:参与活动可以通过提高患者招募和保留率、降低成本以及帮助试验满足监管机构和支付方的期望,来提高临床试验的质量和效率。所有代表都表示,投资包括专门的员工时间和专业知识以及财务资源。在评估利益和投资时还确定了需要考虑的因素,并提出了澄清参与活动清单的建议。
利用这些发现,我们将 31 项参与活动细化为贯穿医疗产品开发生命周期的 24 项独特活动。我们还开发了一个基于网络的优先级工具(https://prioritizationtool.ctti-clinicaltrials.org/),以帮助临床研究赞助商和患者群体确定高优先级的参与活动。该工具的使用可以帮助赞助商和患者群体确定他们认为将提供最大利益的参与活动,同时投入最少的资金,这可能会导致在医疗产品开发中建立更有意义和互利的伙伴关系。