Researcher allegiance in psychotherapy outcome research: An overview of reviews

Researcher allegiance (RA) is widely discussed as a risk of bias in psychotherapy outcome research. The relevance attached to RA bias is related to meta-analyses demonstrating an association of RA with treatment effects. However, recent meta-analyses have yielded mixed results. To provide more clari...

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Veröffentlicht in:Clinical psychology review 2013-06, Vol.33 (4), p.501-511
Hauptverfasser: Munder, Thomas, Brütsch, Oliver, Leonhart, Rainer, Gerger, Heike, Barth, Jürgen
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Sprache:eng
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Zusammenfassung:Researcher allegiance (RA) is widely discussed as a risk of bias in psychotherapy outcome research. The relevance attached to RA bias is related to meta-analyses demonstrating an association of RA with treatment effects. However, recent meta-analyses have yielded mixed results. To provide more clarity on the magnitude and robustness of the RA-outcome association this article reports on a meta-meta-analysis summarizing all available meta-analytic estimates of the RA-outcome association. Random-effects methods were used. Primary study overlap was controlled. Thirty meta-analyses were included. The mean RA-outcome association was r=.262 (p=.002, I2=28.98%), corresponding to a moderate effect size. The RA-outcome association was robust across several moderating variables including characteristics of treatment, population, and the type of RA assessment. Allegiance towards the RA bias hypothesis moderated the RA-outcome association. The findings of this meta-meta-analysis suggest that the RA-outcome association is substantial and robust. Implications for psychotherapy outcome research are discussed. ► An overview of reviews on researcher allegiance and outcome was conducted. ► A substantial association of researcher allegiance and outcome was found. ► Moderator analyses supported the robustness of the allegiance-outcome association. ► Researcher allegiance can be considered a risk of bias in psychotherapy outcome research.
ISSN:0272-7358
1873-7811
DOI:10.1016/j.cpr.2013.02.002