The University of Melbourne, Melbourne, VIC, Australia.
Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Orphanet J Rare Dis. 2024 Sep 5;19(1):322. doi: 10.1186/s13023-024-03320-9.
BACKGROUND/AIM: Leukodystrophies comprise a group of genetic white matter disorders that lead to progressive motor and cognitive impairment. Recent development of novel therapies has led to an increase in clinical trials for leukodystrophies. To enable recruitment of individuals with a leukodystrophy into clinical trials, clinical trial acceptability should be ascertained. We sought therefore, to identify the motivations for and barriers to clinical trial participation in addition to clinical trial features that may be of concern to individuals with a leukodystrophy and/or their carers.
Adults with a leukodystrophy and parents/carers of individuals with a leukodystrophy were recruited through the Australian Leukodystrophy Registry and through online advertisements. Qualitative semi-structured interviews were used to explore participants views on what clinical trials involve, the perceived risks and benefits of clinical trials, their desire to participate in clinical trials and their personal experience with leukodystrophy. Thematic analysis of data was performed with co-coding of interview transcripts.
5 interviews were held with parents of children with leukodystrophy, 4 with parents of adults with leukodystrophy and 3 with adults diagnosed with leukodystrophy. Motivations for clinical trial enrolment include access to potentially lifesaving novel treatments and improved prognostic outcomes. Participants were concerned about adverse clinical trial outcomes, including side effects and exacerbation of illness. Despite this, majority of participants were willing to try anything in clinical trials, demonstrating a high tolerance for first in human trials and trials utilising invasive treatment options.
Interviewees communicated a strong desire to participate in interventional clinical trials involving novel therapies. To support enrolment into future leukodystrophy clinical trials we suggest the provision of transparent information regarding clinical trial treatments, consideration of alternative trial control measures, and inclusion of treating clinicians in the trial recruitment process. Clinicians play an integral role in initiating transparent conversations regarding trial risks and adverse outcomes.
背景/目的:脑白质营养不良是一组遗传性白质疾病,可导致进行性运动和认知障碍。新型治疗方法的最新进展导致脑白质营养不良的临床试验数量增加。为了将脑白质营养不良患者招募到临床试验中,应确定临床试验的可接受性。因此,我们旨在确定除了临床试验特征外,个体参加临床试验的动机和障碍,以及脑白质营养不良患者及其照顾者可能关注的临床试验特征。
通过澳大利亚脑白质营养不良登记处和在线广告招募脑白质营养不良患者及其父母/照顾者。使用定性半结构式访谈来探讨参与者对临床试验的看法,包括对临床试验的风险和益处的看法、参与临床试验的意愿以及他们个人的脑白质营养不良经历。使用协同编码访谈记录对数据进行主题分析。
对患有脑白质营养不良的儿童的父母进行了 5 次访谈,对患有脑白质营养不良的成年患者的父母进行了 4 次访谈,对患有脑白质营养不良的成年患者进行了 3 次访谈。参加临床试验的动机包括获得潜在的救命新型治疗方法和改善预后结果。参与者担心临床试验的不良结果,包括副作用和病情恶化。尽管如此,大多数参与者愿意尝试临床试验中的任何治疗方法,表现出对首次人体试验和使用侵入性治疗方案的试验的高度容忍度。
受访者传达了强烈的愿望,希望参与涉及新型疗法的干预性临床试验。为了支持未来脑白质营养不良临床试验的入组,我们建议提供关于临床试验治疗的透明信息,考虑替代试验对照措施,并让治疗临床医生参与试验招募过程。临床医生在开始关于试验风险和不良结果的透明对话方面发挥着不可或缺的作用。