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The eSMART study protocol: a randomised controlled trial to evaluate electronic symptom management using the advanced symptom management system (ASyMS) remote technology for patients with cancer

机译:eSMART研究方案:一项针对癌症患者使用先进症状管理系统(ASyMS)远程技术评估电子症状管理的随机对照试验

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摘要

Introduction While some evidence exists that real-time remote symptom monitoring devices can decrease morbidity and prevent unplanned admissions in oncology patients, overall, these studies have significant methodological weaknesses. The eSMART study (electronic Symptom Management using the Advanced Symptom Management System (ASyMS) Remote Technology) is designed to specifically address these weaknesses with an appropriately powered, repeated-measures, parallel-group stratified randomised, controlled trial (RCT) of oncology patients. Methods and analysis A total of 1,108 patients scheduled to commence first-line chemotherapy (CTX) for breast, colorectal, or haematological cancer will be recruited from multiple sites across 5 European countries. Patients will be randomised (1:1) to the ASyMS intervention (intervention group) or to standard care currently available at each site (control group). Patients in the control and intervention groups will complete a demographic and clinical questionnaire, as well as a set of valid and reliable electronic patient reported outcome measures (ePROMS) at enrolment, after each of their CTX cycles (up to a maximum of 6 cycles) and at 3, 6, 9 and 12 months after completion of their sixth cycle of CTX. Outcomes that will be assessed include: symptom burden (primary outcome), quality of life (QoL), supportive care needs, anxiety, self-care self-efficacy, work limitations, and cost effectiveness and, from a health professional perspective, changes in clinical practice (secondary outcomes). Ethics and dissemination eSMART received approval from the relevant ethics committees at all of the clinical sites across the 5 participating countries. In collaboration with the European Cancer Patient Coalition (ECPC), the trial results will be disseminated through publications in scientific journals, presentations at international conferences, and postings on the eSMART website and other relevant clinician and consumer websites.
机译:引言尽管有一些证据表明实时远程症状监测设备可以降低肿瘤患者的发病率并防止意外入院,但总体而言,这些研究在方法学上存在明显的缺陷。 eSMART研究(使用高级症状管理系统(ASyMS)远程技术的电子症状管理)旨在通过对肿瘤患者进行适当动力,重复测量,平行分组分层,随机对照试验(RCT)专门解决这些弱点。方法和分析将从欧洲5个国家/地区的多个地点招募总共1,108名计划开始进行乳腺癌,结肠直肠癌或血液学一线化疗(CTX)的患者。患者将被随机分配(1:1)进行ASyMS干预(干预组)或每个站点当前可用的标准护理(对照组)。对照组和干预组的患者在每个CTX周期后(最多6个周期),将在入组时填写一份人口统计学和临床​​调查表,以及一套有效且可靠的电子患者报告的结局指标(ePROMS)。在完成第六个CTX周期后的3、6、9和12个月。将评估的结果包括:症状负担(主要结果),生活质量(QoL),支持护理需求,焦虑,自我护理自我效能,工作限制和成本效益,以及从卫生专业人员的角度来看,临床实践(次要结果)。道德规范和传播eSMART在5个参与国的所有临床场所均获得了相关道德委员会的批准。与欧洲癌症患者联盟(ECPC)合作,将通过科学期刊上的出版物,国际会议上的演示文稿以及在eSMART网站以及其他相关临床医生和消费者网站上发布的内容来传播试验结果。

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