The regression discontinuity design showed to be a valid alternative to a randomized controlled trial for estimating treatment effects

Iris L. Maas, Sandra Nolte, Otto B. Walter, Thomas Berger, Martin Hautzinger, Fritz Hohagen, Wolfgang Lutz, Björn Meyer, Johanna Schröder, Christina Späth, Jan Philipp Klein, Steffen Moritz, Matthias Rose*

*Korrespondierende/r Autor/-in für diese Arbeit
8 Zitate (Scopus)

Abstract

Objectives To compare treatment effect estimates obtained from a regression discontinuity (RD) design with results from an actual randomized controlled trial (RCT). Study Design and Setting Data from an RCT (EVIDENT), which studied the effect of an Internet intervention on depressive symptoms measured with the Patient Health Questionnaire (PHQ-9), were used to perform an RD analysis, in which treatment allocation was determined by a cutoff value at baseline (PHQ-9 = 10). A linear regression model was fitted to the data, selecting participants above the cutoff who had received the intervention (n = 317) and control participants below the cutoff (n = 187). Outcome was PHQ-9 sum score 12 weeks after baseline. Robustness of the effect estimate was studied; the estimate was compared with the RCT treatment effect. Results The final regression model showed a regression coefficient of −2.29 [95% confidence interval (CI): −3.72 to −.85] compared with a treatment effect found in the RCT of −1.57 (95% CI: −2.07 to −1.07). Conclusion Although the estimates obtained from two designs are not equal, their confidence intervals overlap, suggesting that an RD design can be a valid alternative for RCTs. This finding is particularly important for situations where an RCT may not be feasible or ethical as is often the case in clinical research settings.

OriginalspracheEnglisch
ZeitschriftJournal of clinical epidemiology
Jahrgang82
Seiten (von - bis)94-102
Seitenumfang9
ISSN0895-4356
DOIs
PublikationsstatusVeröffentlicht - 01.02.2017

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  • Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)

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