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pmid: 15367237
This paper discusses the relations between different types of patient-reported outcomes that may be collected in clinical studies. Two models are presented that argue that there is a linear relation between the different outcomes. When needs-based quality of life (QoL) is incorporated into the model it is proposed that a two-dimensional relation is more appropriate. The new model is illustrated by data collected using different types of outcome measures. Finally, the different outcomes are related to their purpose in clinical studies.
impairment, Clinical Trials as Topic, Self Disclosure, Psychometrics, Depression, questionnaire, Health Policy, Public Health, Environmental and Occupational Health, patient-reported outcome, disability, quality of life, Surveys and Questionnaires, Outcome Assessment, Health Care, Quality of Life, Humans
impairment, Clinical Trials as Topic, Self Disclosure, Psychometrics, Depression, questionnaire, Health Policy, Public Health, Environmental and Occupational Health, patient-reported outcome, disability, quality of life, Surveys and Questionnaires, Outcome Assessment, Health Care, Quality of Life, Humans
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 20 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |