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

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Show simple item record Maguire, Roma Fox, Patricia A. McCann, Lisa Furlong, Eileen Buick, Alison et al. 2017-09-12T11:47:06Z 2017-09-12T11:47:06Z 2017 the authors en 2017-05
dc.identifier.citation BMJ Open en
dc.description.abstract 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. en
dc.description.sponsorship European Commission - Seventh Framework Programme (FP7) en
dc.language.iso en en
dc.publisher BMJ en
dc.subject Cancer en
dc.subject Chemotherapy en
dc.subject Information technology en
dc.subject Randomised controlled trial en
dc.subject Symptom management en
dc.title 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 en
dc.type Journal Article en
dc.status Peer reviewed en
dc.identifier.volume 7 en
dc.identifier.issue 5 en
dc.identifier.startpage e015016 en
dc.identifier.doi 10.1136/bmjopen-2016-015016
dc.neeo.contributor Maguire|Roma|aut|
dc.neeo.contributor Fox|Patricia A.|aut|
dc.neeo.contributor McCann|Lisa|aut|
dc.neeo.contributor Furlong|Eileen|aut|
dc.neeo.contributor Buick|Alison|aut|
dc.neeo.contributor et al.||aut|
dc.internal.rmsid 764322735 2017-06-18T17:14:47Z

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