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Questionnaires in clinical trials: guidelines for optimal design and administration

Overview of attention for article published in Trials, January 2010
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Title
Questionnaires in clinical trials: guidelines for optimal design and administration
Published in
Trials, January 2010
DOI 10.1186/1745-6215-11-2
Pubmed ID
Authors

Phil Edwards

Abstract

A good questionnaire design for a clinical trial will minimise bias and maximise precision in the estimates of treatment effect within budget. Attempts to collect more data than will be analysed may risk reducing recruitment (reducing power) and increasing losses to follow-up (possibly introducing bias). The mode of administration can also impact on the cost, quality and completeness of data collected. There is good evidence for design features that improve data completeness but further research is required to evaluate strategies in clinical trials. Theory-based guidelines for style, appearance, and layout of self-administered questionnaires have been proposed but require evaluation.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 374 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Denmark 3 <1%
United Kingdom 3 <1%
Italy 2 <1%
Brazil 2 <1%
Bangladesh 1 <1%
Colombia 1 <1%
Australia 1 <1%
Indonesia 1 <1%
Mexico 1 <1%
Other 3 <1%
Unknown 356 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 61 16%
Researcher 60 16%
Student > Master 60 16%
Student > Bachelor 34 9%
Other 25 7%
Other 67 18%
Unknown 67 18%
Readers by discipline Count As %
Medicine and Dentistry 119 32%
Nursing and Health Professions 32 9%
Social Sciences 28 7%
Psychology 21 6%
Agricultural and Biological Sciences 18 5%
Other 78 21%
Unknown 78 21%