230P Physiotherapy for rare hereditary NMDs- an open and free e-learning course for physiotherapists. Results after 18 months online at sjelden.no

IF 2.7 4区 医学 Q2 CLINICAL NEUROLOGY
A. Rosenberger , R. Schandy , S. Lysne , H. Hæstad
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引用次数: 0

Abstract

Physiotherapy is an important modality for patients with neuromuscular disorders, as individually targeted physiotherapy approaches may enhance functions in daily life, and thereby affect quality of life. In Norway, there is scarce knowledge of physiotherapy for neuromuscular patients among physiotherapists (PTs). The PTs at the National Neuromuscular Centre, Norway (NMK), saw the need for the development of free and easily attainable learning resources to empower PTs at hospitals and in communities in their clinical reasoning process. A service development project was conducted, resulting in an e-learning course published at the Norwegian learning platform sjelden.no. The e-learning course was developed in close collaboration with sjelden.no, a learning platform for rare diseases funded by Norwegian National Advisory Unit on Rare Disorders (NKSD). The project period ran from 2018-2022. The course is presented in written and spoken Norwegian and consists of five modules. 1) Introduction 2) Human movement- from healthy to muscle disease 3) Examples of movement analysis of patients 4) Intervention examples 5) Course test with 15 multiple choice questions. The course was published in Sep.2022. Information and advertisement has been provided from NMK at national and international conferences, on NMK's SoMe-platforms and website, and at clinical courses for PTs in Norway. From September 2022-March 2024, the e-learning course has had 2209 users and 3772 views based on statistics from Google Analytics. This is the 3rd most visited learning resource at sjelden.no. The introductory video has 400 full-length finishes, while 120 PTs has passed the course-test. The e-learning course has good statistics of use by Norwegian PTs when looking at users, views and completion of the course test. To enhance the sharing of evidence-based physiotherapy for NMD-patients to PTs, a digital course thus seems to be a cost-effective and potent tool. To enable availability for an international audience, translation to English with publishing through sjelden.no and ERN Euro-NMD is planned for 2024-2025.
230P 罕见遗传性 NMD 的物理治疗--面向物理治疗师的开放式免费电子学习课程。在 sjelden.no 上在线学习 18 个月后的结果
物理治疗是神经肌肉疾病患者的一种重要治疗方式,因为有针对性的物理治疗方法可以增强患者的日常生活功能,从而提高生活质量。在挪威,物理治疗师对神经肌肉疾病患者的物理治疗知之甚少。挪威国家神经肌肉中心(NMK)的物理治疗师们认为有必要开发免费且易于获取的学习资源,以增强医院和社区物理治疗师在临床推理过程中的能力。该中心开展了一个服务开发项目,最终在挪威学习平台sjelden.no上发布了一门电子学习课程。该电子学习课程是与挪威罕见疾病国家咨询机构(NKSD)资助的罕见疾病学习平台sjelden.no密切合作开发的。项目期限为 2018-2022 年。课程以挪威语书面和口语形式呈现,由五个模块组成。1) 简介 2) 人体运动--从健康到肌肉疾病 3) 患者运动分析实例 4) 干预实例 5) 含 15 道选择题的课程测试。该课程于 2022 年 9 月出版。NMK 在国内和国际会议上、NMK 的 SoMe 平台和网站上以及在挪威的 PT 临床课程中提供了相关信息和广告。从 2022 年 9 月到 2024 年 3 月,根据 Google Analytics 的统计数据,该电子学习课程的用户数量为 2209 人,浏览次数为 3772 次。这是sjelden.no网站上访问量排名第三的学习资源。介绍性视频有 400 个完整片段,120 个 PT 通过了课程测试。从用户、浏览量和课程测试完成情况来看,挪威理疗师对电子学习课程的使用情况统计良好。因此,为了加强康复治疗师对NMD患者循证物理治疗方法的分享,数字课程似乎是一种具有成本效益的有效工具。为了向国际受众提供该课程,计划在 2024-2025 年将其翻译成英文,并通过 sjelden.no 和 ERN Euro-NMD 发布。
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
Neuromuscular Disorders
Neuromuscular Disorders 医学-临床神经学
CiteScore
4.60
自引率
3.60%
发文量
543
审稿时长
53 days
期刊介绍: This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies). The Editors welcome original articles from all areas of the field: • Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery). • Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics. • Studies of animal models relevant to the human diseases. The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders.
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