MEMO Research, Division of Molecular and Clinical Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY, UK.
Trials. 2022 Jul 30;23(1):614. doi: 10.1186/s13063-022-06521-4.
Decentralised clinical trials (DCTs) are clinical trials where all or most trial activities occur in or near participants' homes instead of hospitals or research sites. While more convenient for participants, DCTs may offer limited opportunities to build trust with investigators and trial teams. This qualitative analysis explored DCT stakeholder views to inform strategies for maximising participant recruitment, retention, and adherence.
A secondary analysis of original interview transcripts focused on participant engagement: recruitment, retention, and adherence. Semi-structured interviews were conducted with a purposive sample of stakeholders, including trial managers and administrators, investigators, nurses, vendors, and patient representatives. Interview data were coded using a thematic approach to generate descriptive themes.
Forty-eight stakeholders were interviewed. Three components of participant engagement in DCTs were identified: identifying and attracting potential participants, retaining participants and encouraging adherence, and involvement of patients and the public. Interviewees believed that a potential participant's beliefs about research value and their trust in the research team strongly influenced the likelihood of taking part in a DCT. Early involvement of patients was identified as one way to gauge participant priorities. However, perceived burden was seen as a barrier to recruitment. Factors influencing retention and adherence were related to the same underlying motivators that drove recruitment: personal values, circumstances, and burden. Being part of a DCT should not conflict with the original motivations to participate.
Recruitment, retention, and adherence in DCTs are driven by factors that have previously been found to affect conventional clinical trials. Increasing patient and public involvement can address many of these factors. In contrast to conventional trials, DCTs are perceived as requiring greater emphasis on communication, and contact, to engender trust between participants and researchers despite a relative lack of in-person interaction.
去中心化临床试验(DCT)是指所有或大部分试验活动都在参与者家中或附近进行的临床试验,而不是在医院或研究场所进行。虽然对参与者来说更方便,但 DCT 可能为研究人员和试验团队提供的建立信任的机会有限。这项定性分析探讨了 DCT 利益相关者的观点,以提供策略来最大程度地提高参与者的招募、保留和依从性。
对参与者参与度(招募、保留和依从性)的原始访谈记录进行二次分析。采用目的抽样法,对试验经理和管理人员、研究人员、护士、供应商和患者代表等利益相关者进行了半结构化访谈。使用主题方法对访谈数据进行编码,生成描述性主题。
共访谈了 48 位利益相关者。确定了 DCT 中参与者参与的三个组成部分:识别和吸引潜在参与者、保留参与者并鼓励其依从性,以及患者和公众的参与。受访者认为,潜在参与者对研究价值的看法及其对研究团队的信任程度强烈影响他们参与 DCT 的可能性。早期让患者参与被认为是衡量参与者优先事项的一种方式。然而,被认为是招募障碍的是感知负担。影响保留和依从性的因素与推动招募的相同潜在动机有关:个人价值观、情况和负担。参与 DCT 不应与最初参与的动机相冲突。
DCT 中的招募、保留和依从性是由先前发现会影响常规临床试验的因素驱动的。增加患者和公众的参与可以解决其中的许多因素。与常规试验相比,DCT 被认为需要更加注重沟通和联系,尽管缺乏面对面的互动,但要在参与者和研究人员之间建立信任。