Enhancing vaccine clinical trials participation among elderly: challenges and strategies.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-02-03 DOI:10.1186/s13063-025-08754-5
Paul Gillard, Samer Nakhle, Darin Brimhall, Ouzama Henry, Narcisa Mesaros
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引用次数: 0

Abstract

As the fastest growing demographic worldwide, the elderly population is projected to reach nearly 1 billion by 2030 and double the 2022 number by 2050. Despite being the largest consumers of medications, they have been historically underrepresented in clinical trials. However, we are witnessing a promising shift as their participation in trials is on the rise. In fact, recent megatrials enrolling more than 30,000 elderly participants demonstrated the feasibility of large-scale clinical trials involving this very specific population. However, unique challenges, including multi-morbidities, frailty, and ethically sound informed consent in those with cognitive deficits, require continuous careful reassessments and flexibility. Creative and tailored strategies are of paramount importance to bolster elderly trial participation. This paper highlights challenges and shares our experiences on novel methods and success stories associated with the enrollment and retention of elderly individuals in clinical trials. Successful tactics to balance the burden of clinical trial participation with its benefits encompass regular contact, family and friends' engagement, making travel easier or unnecessary, use of digital tools, and building relationships with community organizations. Through innovative strategies that consider the unique needs and limitations of this population, we can achieve successful participation in clinical trials. This will lead to more effective treatments and interventions for our growing elderly population.

加强老年人参与疫苗临床试验:挑战和策略。
作为世界上增长最快的人口,到2030年,老年人口预计将达到近10亿,到2050年将是2022年的两倍。尽管他们是最大的药物消费者,但他们在临床试验中的代表性一直不足。然而,我们正在目睹一个有希望的转变,因为他们参与试验的人数正在上升。事实上,最近招募了3万多名老年人参与者的大型材料证明了针对这一特定人群进行大规模临床试验的可行性。然而,独特的挑战,包括认知缺陷患者的多发病、脆弱性和合乎道德的知情同意,需要持续仔细的重新评估和灵活性。创造性和量身定制的策略对于促进老年人参与试验至关重要。本文强调了老年人临床试验的挑战,并分享了我们在新方法和成功案例方面的经验。平衡临床试验参与负担与益处的成功策略包括定期联系、家人和朋友的参与、使旅行更容易或不必要、使用数字工具以及与社区组织建立关系。通过考虑到这一人群的独特需求和局限性的创新策略,我们可以成功地参与临床试验。这将为我们日益增长的老年人口带来更有效的治疗和干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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