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Robert A. Greevy

Publications and source records attributed to Robert A. Greevy.

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Bounding the local average treatment effect in an instrumental variable analysis of engagement with a mobile intervention

Estimation of local average treatment effects in randomized trials typically requires an assumption known as the exclusion restriction in cases where we are unwilling to rule out unmeasured confounding. Under this assumption, any benefit from treatment would be mediated through the post-randomization variable being conditioned upon, and would be directly attributable to neither the randomization itself nor its latent descendants. Recently, there has been interest in mobile health interventions to provide healthcare support; such studies can feature one-way content and/or two-way content, the latter of which allowing subjects to engage with the intervention in a way that can be objectively measured on a subject-specific level (e.g., proportion of text messages receiving a response). It is hence highly likely that a benefit achieved by the intervention could be explained in part by receipt of the intervention content and in part by engaging with/responding to it. When seeking to characterize average causal effects conditional on post-randomization engagement, the exclusion restriction is therefore all but surely violated. In this paper, we propose a conceptually intuitive sensitivity analysis procedure for this setting that gives rise to sharp bounds on local average treatment effects. A wide array of simulation studies reveal this approach to have very good finite-sample behavior and to recover local average treatment effects under correct specification of the sensitivity parameter. We apply our methodology to a randomized trial evaluating a text message-delivered intervention for Type 2 diabetes self-care.

stat.ME

Second-generation p-values: improved rigor, reproducibility, & transparency in statistical analyses

Verifying that a statistically significant result is scientifically meaningful is not only good scientific practice, it is a natural way to control the Type I error rate. Here we introduce a novel extension of the p-value - a second-generation p-value - that formally accounts for scientific relevance and leverages this natural Type I Error control. The approach relies on a pre-specified interval null hypothesis that represents the collection of effect sizes that are scientifically uninteresting or are practically null. The second-generation p-value is the proportion of data-supported hypotheses that are also null hypotheses. As such, second-generation p-values indicate when the data are compatible with null hypotheses, or with alternative hypotheses, or when the data are inconclusive. Moreover, second-generation p-values provide a proper scientific adjustment for multiple comparisons and reduce false discovery rates. This is an advance for environments rich in data, where traditional p-value adjustments are needlessly punitive. Second-generation p-values promote transparency, rigor and reproducibility of scientific results by a priori specifying which candidate hypotheses are practically meaningful and by providing a more reliable statistical summary of when the data are compatible with alternative or null hypotheses.

stat.ME