Biesty Linda, Sheehan Sarah, Meskell Pauline, Dowling Maura, Glenton Claire, Shepperd Sasha, Chan Xin Hui S, Cox Rebecca, Devane Declan, Booth Andrew, Houghton Catherine
School of Nursing and Midwifery, University of Galway, Galway, Ireland.
Evidence Synthesis Ireland, University of Galway, Galway, Ireland.
Trials. 2024 Dec 19;25(1):837. doi: 10.1186/s13063-024-08670-0.
The COVID-19 pandemic marked a unique period characterised by an extraordinary global virus spread. The collective effort to halt the transmission of the virus led to various public health initiatives, including a variety of COVID-19 vaccine trials. Many of these trials used adaptive methods to address the pandemic's challenges, such as the need for rapid recruitment. These adaptive methods allow for modifications to the trial procedures without undermining the trial's integrity, making the research process more flexible and efficient. However, recruiting participants for vaccine trials remains a considerable challenge. The aim of this qualitative evidence synthesis (QES) is to explore the factors that influence a person's decision to participate in a COVID-19 vaccine trial. Lessons learned from this could help shape future trials' design and conduct, particularly those conducted within a pandemic.
We conducted a systematic search for qualitative studies and mixed methods studies with a qualitative component in the WHO COVID-19 Research Database, MEDLINE, CINAHL, PsycINFO, Epistemomikos, Online Resource for Research in Clinical Trials (ORCCA), and the Cochrane COVID-19 Study Register. We used the best-fit framework synthesis approach and the Social Ecological Model as an a priori framework. We used the GRADE-CERQual approach to assess our confidence in the review findings.
Five studies involving 539 participants were included. One of these studies included participants in a COVID-19 vaccine trial. In three of the studies, participants were asked hypothetically about their attitudes. Another study included people who had either not responded to or declined an invitation to participate in a COVID-19 vaccine trial. We developed six themes outlining the factors that influence a person's decision to participate in a COVID-19 vaccine trial: (1) personal gains, (2) perceived risk, (3) influence of family and community, (4) contributing for others, (5) institutional trust and mistrust, and (6) accessibility of the trial.
This review sheds light on how people perceive the potential personal, family, and community advantages of trial participation and how these perceptions may be weighed against concerns about vaccine safety. The findings also point toward specific aspects of trial methodology to consider when designing COVID-19 vaccine trials.
2019冠状病毒病(COVID-19)大流行标志着一个独特的时期,其特点是病毒在全球范围内异常传播。为阻止病毒传播而做出的集体努力导致了各种公共卫生举措,包括多项COVID-19疫苗试验。这些试验中有许多采用了适应性方法来应对大流行带来的挑战,比如快速招募参与者的需求。这些适应性方法允许在不损害试验完整性的情况下对试验程序进行修改,从而使研究过程更加灵活高效。然而,为疫苗试验招募参与者仍然是一项巨大的挑战。这项定性证据综合分析(QES)的目的是探索影响人们参与COVID-19疫苗试验决策的因素。从中吸取的经验教训有助于塑造未来试验的设计与实施,尤其是在大流行期间进行的试验。
我们在世界卫生组织COVID-19研究数据库、MEDLINE、CINAHL、PsycINFO、Epistemomikos、临床试验研究在线资源(ORCCA)和Cochrane COVID-19研究注册库中系统检索了定性研究以及包含定性成分的混合方法研究。我们采用了最佳拟合框架综合法,并将社会生态模型作为先验框架。我们使用GRADE-CERQual方法来评估我们对综述结果的信心。
纳入了五项涉及539名参与者的研究。其中一项研究的参与者来自一项COVID-19疫苗试验。在三项研究中,参与者被假设性地询问了他们的态度。另一项研究纳入了未回应或拒绝参与COVID-19疫苗试验邀请的人群。我们梳理出六个主题,概述了影响人们参与COVID-19疫苗试验决策的因素:(1)个人收益,(2)感知风险,(3)家庭和社区的影响,(4)为他人做贡献,(5)对机构的信任与不信任,以及(6)试验的可及性。
本综述揭示了人们如何看待参与试验的潜在个人、家庭和社区益处,以及这些看法如何与对疫苗安全性的担忧进行权衡。研究结果还指出了在设计COVID-19疫苗试验时需要考虑的试验方法的具体方面。