Questionnaires in clinical trials: guidelines for optimal design and administration

Author:

Edwards Phil

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Medicine (miscellaneous)

Reference29 articles.

1. Armstrong BG: Optimizing power in allocating resources to exposure assessment in an epidemiologic study. Am J Epidemiol. 1996, 144: 192-197.

2. Hill AB: Observation and experiment. N Engl J Med. 1953, 248: 995-1001. 10.1056/NEJM195306112482401.

3. Edwards PJ, Roberts I, Clarke MJ, DiGuiseppi C, Wentz R, Kwan I, Cooper R, Felix LM, Pratap S: Methods to increase response to postal and electronic questionnaires. Cochrane Database Syst Rev. 2009, 3: MR000008-

4. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use: ICH harmonised tripartite guideline, statistical principles for clinical trials E9. http://www.ich.org/LOB/media/MEDIA485.pdf

5. CIOMS: Management of safety information from clinical trials: report of CIOMS working group VI. 2005, Geneva, Switzerland: Council for International Organisations of Medical Sciences (CIOMS)

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