Electronic Patient Reported Outcomes
Strategies to use tablet computers for collection of electronic patient-reported outcomes
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<p>Patient Perspective in the Development of Electronic Patient-Reported Outcomes (ePROs) in Seizure Disorders: A Patient-Centric Approach</p>
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Feasibility test of a UK scalable electronic system for regular collection of patient reported outcome measures and linkage with clinical cancer registry data: the electronic Patient reported Outcomes from Cancer Survivors (ePOCS) system
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Feasibility test of a UK-scalable electronic system for regular collection of patient-reported outcome measures and linkage with clinical cancer registry data: The electronic Patient-reported Outcomes from Cancer Survivors (ePOCS) system
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Integrating Patient Reported Outcomes with Clinical Cancer Registry Data: A Feasibility Study of the Electronic Patient-Reported Outcomes from Cancer Survivors (ePOCS) system.
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Evaluating the psychometric properties of an e-based version of the 39-item Parkinson’s Disease Questionnaire
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Oh, the Places We’ll Go: Patient-Reported Outcomes and Electronic Health Records
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Bilateral mammoplasty for cancer: Surgical, oncological and patient-reported outcomes.
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Patient-reported outcomes in neurofibromatosis and schwannomatosis clinical trials
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Proceedings of Patient Reported Outcome Measure’s (PROMs) Conference Sheffield 2016: advances in patient reported outcomes research
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Proceedings of Patient Reported Outcome Measure’s (PROMs) Conference Oxford 2017: Advances in Patient Reported Outcomes Research
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Developing core outcomes sets: methods for identifying and including patient reported outcomes (PROs)
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Requirements for the collection of electronic PROMS either “in clinic” or “at home” as part of the PROMs, PREMs and Effectiveness Programme (PPEP) in Wales: a feasibility study using a generic PROM tool
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<p>Correlations between patient-reported outcomes and self-reported characteristics in adults with hemophilia B and caregivers of children with hemophilia B: analysis of the B-HERO-S study</p>
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Application of Bother in patient reported outcomes instruments across cultures
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Potential of patient-reported outcomes as nonprimary endpoints in clinical trials
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Measuring what matters to rare disease patients – reflections on the work by the IRDiRC taskforce on patient-centered outcome measures
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Strategies for incorporating patient-reported outcomes in the care of people with chronic kidney disease (PRO kidney): a protocol for a realist synthesis
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Evaluation of electronic patient-reported outcome assessment with cancer patients in the hospital and at home
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