Randomization
is a practice used to assign subjects
to experimental groups in a research
study.
For example, consider a fictitious research
study meant to compare the effectiveness of a new drugs for
reducing blood pressure. The researchers will recruit a number
of participants or subjects, making every attempt to make
sure the participants are as similar as possible (similar
medical histories, similar pre-existing blood pressure, etc.).
Then the researchers will randomly assign each subject to
either the experimental or the control
group -- for example, by flipping a coin. Subjects in
the experimental group will take the new drug for a number
of weeks; subjects in the control group will take an inactive
compound or placebo
for comparison. At the end of some period, the researchers
will then test blood pressure in all subjects, to see if those
subjects who took the new drug have lower blood pressure,
on average, than subjects who took the placebo. If so, this
would imply that the new drug is effective for lowering blood
pressure.
The practice of randomization is one way to help make sure
that there are no preexisting differences between the subjects
in each group. That way, any differences in blood pressure
at the end of the study can reasonably be attributed to the
effects of the drug being evaluated -- and not to some inadvertent
bias on the part of the researcher for assigning people to
one group or the other. Well-designed research studies, particularly
clinical trials
of new drugs, usually employ randomization, placebo controls
and double-blind
techniques.
Further Reading: "Putting
Ginkgo to the Test"
by Catherine E. Myers. Copyright © 2006 Memory Loss and the Brain
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