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    J Clin Epidemiol. 2011 Nov;64(11):1223-9. Epub 2011 Apr 23.

    Placebo effect studies are susceptible to response bias and to other types of biases.

    Source

    The Nordic Cochrane Centre, Rigshospitalet, Copenhagen, Denmark. ah@cochrane.dk

    Abstract

    OBJECTIVE:

    Investigations of the effect of placebo are often challenging to conduct and interpret. The history of placebo shows that assessment of its clinical significance has a real potential to be biased. We analyze and discuss typical types of bias in studies on placebo.

    STUDY DESIGN AND SETTING:

    A methodological analysis and discussion.

    RESULTS:

    The inherent nonblinded comparison between placebo and no-treatment is the best research design we have in estimating effects of placebo, both in a clinical and in an experimental setting, but the difference between placebo and no-treatment remains an approximate and fairly crude reflection of the true effect of placebo interventions. A main problem is response bias in trials with outcomes that are based on patients' reports. Other biases involve differential co-intervention and patient dropouts, publication bias, and outcome reporting bias. Furthermore, extrapolation of results to a clinical settings are challenging because of a lack of clear identification of the causal factors in many clinical trials, and the nonclinical setting and short duration of most laboratory experiments.

    CONCLUSIONS:

    Creative experimental efforts are needed to assess rigorously the clinical significance of placebo interventions and investigate the component elements that may contribute to the therapeutic benefit.

    Copyright © 2011 Elsevier Inc. All rights reserved.

    PMID:
    21524568
    [PubMed - indexed for MEDLINE]
    PMCID:
    PMC3146959
    [Available on 2012/11/1]

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