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肌萎缩侧索硬化症的研究准入障碍。

Research access barriers in amyotrophic lateral sclerosis.

作者信息

Giacomelli Elisa, Scirocco Erica, Higgins Max, Pilja Arian, Paganoni Sabrina, Ho Doreen

机构信息

Sean M. Healey and AMG Center for ALS & the Neurological Clinical Research Institute, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Harvard Medical School, Spaulding Rehabilitation Hospital, Boston, MA, USA.

出版信息

Amyotroph Lateral Scler Frontotemporal Degener. 2025 Jul 31:1-8. doi: 10.1080/21678421.2025.2539900.

Abstract

As the general population ages, amyotrophic lateral sclerosis (ALS) incidence and prevalence are expected to rise, and the barriers that limit participation in ALS clinical research studies may increase. In this report, we highlight key challenges and available resources for accessing clinical research. We emphasize the importance of education and engagement among individuals with ALS and their families, clinicians, and researchers. Addressing accessibility and fostering trust in ALS research participation is essential to advance treatments for this devastating disease. We propose practical strategies to overcome participation barriers, including decentralized trial models, remote participation options, and expanded outreach through patient navigators, advisory committees, and digital tools. Strengthening partnerships among individuals with ALS, caregivers, researchers, ALS organizations, regulators, and industry, will help align research efforts with community needs and accelerate therapeutic development.

摘要

随着普通人群老龄化,预计肌萎缩侧索硬化症(ALS)的发病率和患病率将会上升,而限制参与ALS临床研究的障碍可能也会增加。在本报告中,我们重点介绍了参与临床研究的关键挑战和可用资源。我们强调了ALS患者及其家属、临床医生和研究人员进行教育和参与的重要性。解决ALS研究参与的可及性问题并增强信任对于推进针对这种毁灭性疾病的治疗至关重要。我们提出了克服参与障碍的实用策略,包括去中心化试验模式、远程参与选项,以及通过患者导航员、咨询委员会和数字工具扩大宣传范围。加强ALS患者、护理人员、研究人员、ALS组织、监管机构和行业之间的伙伴关系,将有助于使研究工作与社区需求保持一致,并加速治疗开发。

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