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Designing Clinical Research, 4ed. [Hulley - LIPPINCOTT Williams and Wilkins]

ISBN/EAN
9781608318049
Editore
LIPPINCOTT Williams and Wilkins
Formato
Brossura
Anno
2013
Edizione
4
Pagine
378

Disponibile

90,00 €
Designing Clinical Research has been extensively revised and continues to set the standard as a practical guide for doctors, nurses, pharmacists, and other health professionals involved in all forms of clinical, translational, and public health research. It presents advanced epidemiologic concepts in a reader-friendly way, and suggests common sense approaches to the challenging judgments involved in designing, funding, and implementing. New to this edition: Expanded and updated content in every chapter, with new material on: • non-inferiority trials for comparative effectiveness research • incidence-density case-control studies • confounding and effect modification • diagnostic test studies to inform prediction rules • ethical aspects of whole genome sequencing • automated data management approaches • new NIH grant-writing requirements Color format, and Electronic access, powered by Inkling™ as a free companion to the text • viewable through your browser or as a download to tablet or smartphone • the complete text with optimized navigation • note-sharing, highlighting and bookmarking capability • cross-linking of references and content • rapid search options linked to the new glossary

Maggiori Informazioni

Autore Hulley Stephen B.; Cummings Steven R.; Browner Warren S.; Grady Deborah G.; Newman Thomas B.
Editore LIPPINCOTT Williams and Wilkins
Anno 2013
Tipologia Libro
Lingua Inglese
Indice Section I Basic Ingredients 1 Getting Started: The Anatomy and Physiology of Clinical Research Stephen B. Hulley, Thomas B. Newman, and Steven R. Cummings 2 Conceiving the Research Question and Developing the Study Plan Steven R. Cummings, Warren S. Browner, and Stephen B. Hulley 3 Choosing the Study Subjects: Specification, Sampling, and Recruitment Stephen B. Hulley, Thomas B. Newman, and Steven R. Cummings 4 Planning the Measurements: Precision, Accuracy and Validity Stephen B. Hulley, Thomas B. Newman and Steven R. Cummings 5 Getting Ready to Estimate Sample Size: Hypotheses and Underlying Principles Warren S. Browner, Thomas B. Newman, and Stephen B. Hulley 6 Estimating Sample Size and Power: Applications and Examples Warren S. Browner, Thomas B. Newman, and Stephen B. Hulley Section II Study Designs 7 Designing Cross-Sectional and Cohort Studies Stephen B. Hulley, Steven R. Cummings, and Thomas B. Newman 8 Designing Case–Control Studies Thomas B.Newman, Warren S.Browner, Steven R.Cummings, and Stephen B.Hulley 9 Enhancing Causal Inference in Observational Studies Thomas B. Newman, Warren S. Browner, and Stephen B. Hulley 10 Designing a Randomized Blinded Trial Steven R. Cummings, Deborah Grady, and Stephen B. Hulley 11 Alternative Trial Designs and Implementation Issues Deborah Grady, Steven R. Cummings, and Stephen B. Hulley 12 Designing Studies of Medical Tests Thomas B.Newman, Warren S.Browner, Steven R.Cummings, and Stephen B. Hulley 13 Research Using Existing Data Deborah Grady, Steven R. Cummings and Stephen B. Hulley Section III Implementation 14 Addressing Ethical Issues Bernard Lo and Deborah Grady 15 Designing Questionnaires, Interviews and Online Surveys Steven R. Cummings, Michael A. Kohn, and Stephen B. Hulley 16 Data Management Michael A. Kohn, Thomas B. Newman, and Stephen B. Hulley 17 Implementing the Study and Quality Control Deborah Grady and Stephen B. Hulley 18 Community and International Studies Norman Hearst and Thomas Novotny 19 Writing and Funding a Research Proposal Steven R. Cummings and Stephen B. Hulley Exercises Answers to Exercises Glossary
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