2012
DOI: 10.2196/jmir.2214
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Electronic Symptom Reporting Between Patient and Provider for Improved Health Care Service Quality: A Systematic Review of Randomized Controlled Trials. Part 1: State of the Art

Abstract: BackgroundOver the last two decades, the number of studies on electronic symptom reporting has increased greatly. However, the field is very heterogeneous: the choices of patient groups, health service innovations, and research targets seem to involve a broad range of foci. To move the field forward, it is necessary to build on work that has been done and direct further research to the areas holding most promise. Therefore, we conducted a comprehensive review of randomized controlled trials (RCTs) focusing on … Show more

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Cited by 53 publications
(65 citation statements)
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References 93 publications
(115 reference statements)
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“…Electronic health records and mobile consumer technologies may aid these efforts. 43,44 From a literacy perspective, using technology for action plans or other engagement activities would increase the proficiency required by patients to assume self-care roles. The result might widen literacy disparities in knowledge, behavior, and outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…Electronic health records and mobile consumer technologies may aid these efforts. 43,44 From a literacy perspective, using technology for action plans or other engagement activities would increase the proficiency required by patients to assume self-care roles. The result might widen literacy disparities in knowledge, behavior, and outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…At the individual level, a majority of those who access health information online found the information useful (92%) and learned something new (81%) [24]. Online health information seekers also reported greater level of empowerment and awareness of their role in their health [3,10,[24][25][26]. Approximately 80% sought health information online for convenience, the volume of recent health information available, and the anonymity [27].…”
Section: Introductionmentioning
confidence: 99%
“…12,13 Moreover, evidence suggests that patient-reported outcome measures (PROMs) enable patient-centered care that guides the clinical decisionmaking process. 14,15 Therefore, COS should be a composite of both clinically observed indicators as well as PROMs, as recommended in a number of recent outcome initiatives, such as Outcome Measures in Rheumatology (OMERACT) and Core Outcome Measures in Effectiveness Trials (COMET). 13,15 The OMERACT Filter 2.0 is a framework for researchers to determine what outcomes should be measured, how they should be measured, and for deciding which outcomes should be selected when creating a COS. Envisioned in 1992 and continually developed through consensus-driven discussion, OMERACT was established as a procedural framework for the identification and selection of valid, responsive, and feasible rheumatologic outcomes in clinical trials.…”
mentioning
confidence: 99%