Centre for Trials Research, Cardiff University, 4th floor Neuadd Meirionnydd, Heath Park, Cardiff, CF14 4YS, UK.
Division of Population Medicine, School of Medicine, Cardiff University, 8th floor Neuadd Meirionnydd, Heath Park, Cardiff, UK.
Trials. 2022 Sep 6;23(1):756. doi: 10.1186/s13063-022-06705-y.
The number of interventions to improve recruitment and retention of participants in trials is rising, with a corresponding growth in randomised Studies Within Trials (SWATs) to evaluate their (cost-)effectiveness. Despite recognised challenges in conducting trials involving adults who lack capacity to consent, until now, no individual-level recruitment interventions have focused on this population. Following the development of a decision aid for family members making non-emergency trial participation decisions on behalf of people with impaired capacity, we have designed a SWAT to evaluate the decision aid in a number of host trials (CONSULT). Unlike in recruitment SWATs to date, the CONSULT intervention is aimed at a 'proxy' decision-maker (a family member) who is not a participant in the host trial and does not receive the trial intervention. This commentary explores the methodological and ethical considerations encountered when designing such SWATs, using the CONSULT SWAT as a case example. Potential solutions to address these issues are also presented.
We encountered practical issues around informed consent, data collection, and follow-up which involves linking the intervention receiver (the proxy) with recruitment and retention data from the host trial, as well as issues around randomisation level, resource use, and maintaining the integrity of the host trial. Unless addressed, methodological uncertainty about differential recruitment and heterogeneity between trial populations could potentially limit the scope for drawing robust inferences and harmonising data from different SWAT host trials. Proxy consent is itself ethically complex, and so when conducting a SWAT which aims to disrupt and enhance proxy consent decisions, there are additional ethical issues to be considered.
Designing a SWAT to evaluate a recruitment intervention for non-emergency trials with adults lacking capacity to consent has raised a number of methodological and ethical considerations. Explicating these challenges, and some potential ways to address them, creates a starting point for discussions about conducting these potentially more challenging SWATs. Increasing the evidence base for the conduct of trials involving adults lacking capacity to consent is intended to improve both the ability to conduct these trials and their quality, and so help build research capacity for this under-served population.
为了提高试验参与者的招募和保留率,干预措施的数量不断增加,同时也相应地增加了旨在评估其(成本)效益的试验内随机对照研究(SWAT)。尽管在涉及缺乏同意能力的成年人的试验中存在公认的挑战,但迄今为止,尚无针对该人群的个别干预措施来专门解决招募问题。在为缺乏能力的人制定了一项用于代表他们做出非紧急试验参与决策的家属决策辅助工具之后,我们设计了一项 SWAT,以在多个宿主试验(CONSULT)中评估该决策辅助工具。与迄今为止的招募 SWAT 不同,CONSULT 干预措施的目标是“代理人”决策者(家属),他们不是宿主试验的参与者,也不接受试验干预。本文使用 CONSULT SWAT 作为案例示例,探讨了在设计此类 SWAT 时遇到的方法学和伦理问题。还提出了一些潜在的解决方案来解决这些问题。
我们遇到了与知情同意、数据收集和随访相关的实际问题,这些问题涉及将干预措施的接受者(代理人)与宿主试验的招募和保留数据联系起来,以及涉及随机化水平、资源利用和保持宿主试验完整性的问题。除非得到解决,否则关于试验人群之间不同招募和异质性的方法学不确定性可能会限制从不同 SWAT 宿主试验中得出可靠推断和协调数据的范围。代理同意本身在伦理上就很复杂,因此,当进行旨在扰乱和增强代理同意决策的 SWAT 时,还需要考虑其他伦理问题。
设计一项用于评估非紧急试验中缺乏同意能力的成年人的招募干预措施的 SWAT 提出了一些方法学和伦理问题。阐明这些挑战以及一些潜在的解决方法为讨论进行这些潜在更具挑战性的 SWAT 提供了起点。增加涉及缺乏同意能力的成年人的试验实施的证据基础旨在提高这些试验的实施能力和质量,从而帮助为这个服务不足的人群建立研究能力。