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Inconsistencies in Quality of Life Data Collection in Clinical Trials: A Potential Source of Bias? Interviews with Research Nurses and Trialists

Overview of attention for article published in PLOS ONE, October 2013
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Title
Inconsistencies in Quality of Life Data Collection in Clinical Trials: A Potential Source of Bias? Interviews with Research Nurses and Trialists
Published in
PLOS ONE, October 2013
DOI 10.1371/journal.pone.0076625
Pubmed ID
Authors

Derek Kyte, Jonathan Ives, Heather Draper, Thomas Keeley, Melanie Calvert

Abstract

Patient-reported outcomes (PROs), such as health-related quality of life (HRQL) are increasingly used to evaluate treatment effectiveness in clinical trials, are valued by patients, and may inform important decisions in the clinical setting. It is of concern, therefore, that preliminary evidence, gained from group discussions at UK-wide Medical Research Council (MRC) quality of life training days, suggests there are inconsistent standards of HRQL data collection in trials and appropriate training and education is often lacking. Our objective was to investigate these reports, to determine if they represented isolated experiences, or were indicative of a potentially wider problem.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 68 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 1%
Spain 1 1%
Unknown 66 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 9 13%
Researcher 8 12%
Student > Bachelor 7 10%
Student > Master 6 9%
Other 5 7%
Other 15 22%
Unknown 18 26%
Readers by discipline Count As %
Medicine and Dentistry 17 25%
Nursing and Health Professions 9 13%
Unspecified 5 7%
Social Sciences 5 7%
Agricultural and Biological Sciences 2 3%
Other 10 15%
Unknown 20 29%