A written protocol is vital before conducting research, and should consist of sections on preliminary comments, subjects and methods, details of interventions and outcome measures, and methods of analysis. The process of developing the protocol provides a disciplined consideration of all aspects of the study.
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References
1.
Committee for Proprietary Medicinal Products (CPMP)Working Party on Efficacy of Medicinal Products. Good clinical practice for trials on medicinal products in the European Community: EEC notes for guidance. Pharmacology & Toxicology1990; 67: 361–72.
2.
Editorial. Denmark takes a lead on research ethics. British Medical Journal1998; 316: 1189.
3.
AltmanDG. Practical Statistics for Medical Research. 1 st ed. London: Chapman and Hall; 1991. p.455–60.
4.
FilshieJ, CummingsTM. Western medical acupuncture. In: ErnstE, WhiteAR, editors. Acupuncture: A Scientific Appraisal.Oxford: Butterworth-Heinemann; 1999.
5.
MotulskyH.Intuitive Biostatistics.Oxford: Oxford University Press1995; p.298.