Abstract
Abstract
Micro-randomized trials (MRTs) provide a framework for evaluating the marginal and moderated effects of mobile health (mHealth) interventions. In many applications, treatments take the form of categorical variables with multiple levels, such as different message contents or delivery strategies. Many scientifically meaningful longitudinal outcomes in mHealth studies are binary, such as whether a participant opens an app, engages with content, or completes a target behavior following a decision point at which treatment is randomized. This paper focuses on MRTs with categorical treatments and binary proximal outcomes. We define the causal excursion effect, propose an estimator called EMEE-catA, and derive a sample size formula for comparing categorical treatment levels that controls the type I error rate and guarantees power under working assumptions. We conduct extensive simulation studies to evaluate the operating characteristics of the proposed sample size formula, including robustness to violations of these assumptions. We further provide practical guidance for implementing the proposed approach to ensure adequate power in real-world MRTs. The methods are illustrated using data from the Drink Less MRT.