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Daniel Almirall

Publications and source records attributed to Daniel Almirall.

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Q-Learning with Clustered-SMART (cSMART) Data: Examining Moderators in the Construction of Clustered Adaptive Interventions

A clustered adaptive intervention (cAI) is a pre-specified sequence of decision rules that guides practitioners on how best - and based on which measures - to tailor cluster-level intervention to improve outcomes at the level of individuals within the clusters. A clustered sequential multiple assignment randomized trial (cSMART) is a type of trial that is used to inform the empirical development of a cAI. The most common type of secondary aim in a cSMART focuses on assessing causal effect moderation by candidate tailoring variables. We introduce a clustered Q-learning framework with the M-out-of-N Cluster Bootstrap using data from a cSMART to evaluate whether a set of candidate tailoring variables may be useful in defining an optimal cAI. This approach could construct confidence intervals (CI) with near-nominal coverage to assess parameters indexing the causal effect moderation function. Specifically, it allows reliable inferences concerning the utility of candidate tailoring variables in constructing a cAI that maximizes a mean end-of-study outcome even when "non-regularity", a well-known challenge exists. Simulations demonstrate the numerical performance of the proposed method across varying non-regularity conditions and investigate the impact of varying number of clusters and intra-cluster correlation coefficient on CI coverage. Methods are applied on ADEPT dataset to inform the construction of a clinic-level cAI for improving evidence-based practice in treating mood disorders.

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Multilevel Primary Aim Analyses of Clustered SMARTs: With Applications in Health Policy

In many health policy settings, adaptive interventions target a population of clusters (e.g., schools), with the ultimate intent of impacting outcomes at the level of individuals within the clusters. Health policy researchers can use clustered, sequential, multiple assignment, randomized trials (SMARTs) to answer important scientific questions concerning clustered adaptive interventions. A common primary aim is to compare the mean of a nested, end-of-study outcome between two clustered adaptive interventions. However, existing methods are not suitable when the primary outcome in a clustered SMART is nested and longitudinal (e.g., repeated outcome measures nested within mental healthcare providers, and mental healthcare providers nested within schools). This manuscript proposes a three-level marginal mean modeling and estimation approach for comparing adaptive interventions in a clustered SMART. The proposed method enables policy analysts to answer a wider array of scientific questions in the marginal comparison of clustered adaptive interventions. Further, relative to using an existing two-level method with a nested end-of-study outcome, the proposed method benefits from improved statistical efficiency. With this approach, we examine longitudinal comparisons of adaptive interventions for improving school-based mental healthcare and contrast its performance with existing approaches for studying static end-of-study outcomes. Methods were motivated by the Adaptive School-Based Implementation of CBT (ASIC) study, a clustered SMART designed to construct an adaptive health policy to improve the adoption of evidence-based CBT by mental healthcare professionals in high schools across Michigan.

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Finite-sample adjustments for comparing clustered adaptive interventions using data from a clustered SMART

Adaptive interventions, aka dynamic treatment regimens, are sequences of pre-specified decision rules that guide the provision of treatment for an individual given information about their baseline and evolving needs, including in response to prior intervention. Clustered adaptive interventions (cAIs) extend this idea by guiding the provision of intervention at the level of clusters (e.g., clinics), but with the goal of improving outcomes at the level of individuals within the cluster (e.g., clinicians or patients within clinics). A clustered, sequential multiple-assignment randomized trials (cSMARTs) is a multistage, multilevel randomized trial design used to construct high-quality cAIs. In a cSMART, clusters are randomized at multiple intervention decision points; at each decision point, the randomization probability can depend on response to prior data. A challenge in cluster-randomized trials, including cSMARTs, is the deleterious effect of small samples of clusters on statistical inference, particularly via estimation of standard errors. \par This manuscript develops finite-sample adjustment (FSA) methods for making improved statistical inference about the causal effects of cAIs in a cSMART. The paper develops FSA methods that (i) scale variance estimators using a degree-of-freedom adjustment, (ii) reference a t distribution (instead of a normal), and (iii) employ a ``bias corrected" variance estimator. Method (iii) requires extensions that are unique to the analysis of cSMARTs. Extensive simulation experiments are used to test the performance of the methods. The methods are illustrated using the Adaptive School-based Implementation of CBT (ASIC) study, a cSMART designed to construct a cAI for improving the delivery of cognitive behavioral therapy (CBT) by school mental health professionals within high schools in Michigan.

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Approaches to Statistical Efficiency when comparing the embedded adaptive interventions in a SMART

Sequential, multiple assignment randomized trials (SMARTs), which assist in the optimization of adaptive interventions, are growing in popularity in education and behavioral sciences. This is unsurprising, as adaptive interventions reflect the sequential, tailored nature of learning in a classroom or school. Nonetheless, as is true elsewhere in education research, observed effect sizes in education-based SMARTs are frequently small. As a consequence, statistical efficiency is of paramount importance in their analysis. The contributions of this manuscript are two-fold. First, we provide an overview of adaptive interventions and SMART designs for researchers in education science. Second, we propose four techniques that have the potential to improve statistical efficiency in the analysis of SMARTs. We demonstrate the benefits of these techniques in SMART settings both through the analysis of a SMART designed to optimize an adaptive intervention for increasing cognitive behavioral therapy delivery in school settings and through a comprehensive simulation study. Each of the proposed techniques is easily implementable, either with over-the-counter statistical software or through R code provided in an online supplement.

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SMART Binary: Sample Size Calculation for Comparing Adaptive Interventions in SMART studies with Longitudinal Binary Outcomes

Sequential Multiple-Assignment Randomized Trials (SMARTs) play an increasingly important role in psychological and behavioral health research. This experimental approach enables researchers to answer scientific questions about how to sequence and match interventions to the unique, changing needs of individuals. A variety of sample size planning resources for SMART studies have been developed in recent years; these enable researchers to plan SMARTs for addressing different types of scientific questions. However, relatively limited attention has been given to planning SMARTs with binary (dichotomous) outcomes, which often require higher sample sizes relative to continuous outcomes. Existing resources for estimating sample size requirements for SMARTs with binary outcomes do not consider the potential to improve power by including a baseline measurement and/or multiple repeated outcome measurements. The current paper addresses this issue by providing sample size simulation code and approximate formulas for two-wave repeated measures binary outcomes (i.e., two measurement times for the outcome variable, before and after receiving the intervention). The simulation results agree well with the formulas. We also discuss how to use simulations to calculate power for studies with more than two outcome measurement occasions. The results show that having at least one repeated measurement of the outcome can substantially improve power under certain conditions.

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Estimating Time-Varying Causal Excursion Effect in Mobile Health with Binary Outcomes

Advances in wearables and digital technology now make it possible to deliver behavioral mobile health interventions to individuals in their everyday life. The micro-randomized trial (MRT) is increasingly used to provide data to inform the construction of these interventions. In an MRT, each individual is repeatedly randomized among multiple intervention options, often hundreds or even thousands of times, over the course of the trial. This work is motivated by multiple MRTs that have been conducted, or are currently in the field, in which the primary outcome is a longitudinal binary outcome. The primary aim of such MRTs is to examine whether a particular time-varying intervention has an effect on the longitudinal binary outcome, often marginally over all but a small subset of the individual's data. We propose the definition of causal excursion effect that can be used in such primary aim analysis for MRTs with binary outcomes. Under rather restrictive assumptions one can, based on existing literature, derive a semiparametric, locally efficient estimator of the causal effect. We, starting from this estimator, develop an estimator that can be used as the basis of a primary aim analysis under more plausible assumptions. Simulation studies are conducted to compare the estimators. We illustrate the developed methods using data from the MRT, BariFit. In BariFit, the goal is to support weight maintenance for individuals who received bariatric surgery.

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Sample size considerations for comparing dynamic treatment regimens in a sequential multiple-assignment randomized trial with a continuous longitudinal outcome

Clinicians and researchers alike are increasingly interested in how best to personalize interventions. A dynamic treatment regimen (DTR) is a sequence of pre-specified decision rules which can be used to guide the delivery of a sequence of treatments or interventions that are tailored to the changing needs of the individual. The sequential multiple-assignment randomized trial (SMART) is a research tool which allows for the construction of effective DTRs. We derive easy-to-use formulae for computing the total sample size for three common two-stage SMART designs in which the primary aim is to compare mean end-of-study outcomes for two embedded DTRs which recommend different first-stage treatments. The formulae are derived in the context of a regression model which leverages information from a longitudinal outcome collected over the entire study. We show that the sample size formula for a SMART can be written as the product of the sample size formula for a standard two-arm randomized trial, a deflation factor that accounts for the increased statistical efficiency resulting from a longitudinal analysis, and an inflation factor that accounts for the design of a SMART. The SMART design inflation factor is typically a function of the anticipated probability of response to first-stage treatment. We review modeling and estimation for DTR effect analyses using a longitudinal outcome from a SMART, as well as the estimation of standard errors. We also present estimators for the covariance matrix for a variety of common working correlation structures. Methods are motivated using the ENGAGE study, a SMART aimed at developing a DTR for increasing motivation to attend treatments among alcohol- and cocaine-dependent patients.

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Linear Mixed Models for Comparing Dynamic Treatment Regimens on a Longitudinal Outcome in Sequentially Randomized Trials

A dynamic treatment regimen (DTR) is a pre-specified sequence of decision rules which maps baseline or time-varying measurements on an individual to a recommended intervention or set of interventions. Sequential multiple assignment randomized trials (SMARTs) represent an important data collection tool for informing the construction of effective DTRs. A common primary aim in a SMART is the marginal mean comparison between two or more of the DTRs embedded in the trial. This manuscript develops a mixed effects modeling and estimation approach for these primary aim comparisons based on a continuous, longitudinal outcome. The method is illustrated using data from a SMART in autism research.

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Assessing Time-Varying Causal Effect Moderation in Mobile Health

In mobile health interventions aimed at behavior change and maintenance, treatments are provided in real time to manage current or impending high risk situations or promote healthy behaviors in near real time. Currently there is great scientific interest in developing data analysis approaches to guide the development of mobile interventions. In particular data from mobile health studies might be used to examine effect moderators-i.e., individual characteristics, time-varying context or past treatment response that moderate the effect of current treatment on a subsequent response. This paper introduces a formal definition for moderated effects in terms of potential outcomes, a definition that is particularly suited to mobile interventions, where treatment occasions are numerous, individuals are not always available for treatment, and potential moderators might be influenced by past treatment. Methods for estimating moderated effects are developed and compared. The proposed approach is illustrated using BASICS-Mobile, a smartphone-based intervention designed to curb heavy drinking and smoking among college students.

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Comparing cluster-level dynamic treatment regimens using sequential, multiple assignment, randomized trials: Regression estimation and sample size considerations

Cluster-level dynamic treatment regimens can be used to guide sequential, intervention or treatment decision-making at the cluster level in order to improve outcomes at the individual or patient-level. In a cluster-level DTR, the intervention or treatment is potentially adapted and re-adapted over time based on changes in the cluster that could be impacted by prior intervention, including based on aggregate measures of the individuals or patients that comprise it. Cluster-randomized sequential multiple assignment randomized trials (SMARTs) can be used to answer multiple open questions preventing scientists from developing high-quality cluster-level DTRs. In a cluster-randomized SMART, sequential randomizations occur at the cluster level and outcomes are at the individual level. This manuscript makes two contributions to the design and analysis of cluster-randomized SMARTs: First, a weighted least squares regression approach is proposed for comparing the mean of a patient-level outcome between the cluster-level DTRs embedded in a SMART. The regression approach facilitates the use of baseline covariates which is often critical in the analysis of cluster-level trials. Second, sample size calculators are derived for two common cluster-randomized SMART designs for use when the primary aim is a between-DTR comparison of the mean of a continuous patient-level outcome. The methods are motivated by the Adaptive Implementation of Effective Programs Trial, which is, to our knowledge, the first-ever cluster-randomized SMART in psychiatry.

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Do CRM Systems Cause One-to-One Marketing Effectiveness?

This article provides an assessment of the causal effect of customer relationship management (CRM) applications on one-to-one marketing effectiveness. We use a potential outcomes based propensity score approach to assess this causal effect. We find that firms using CRM systems have greater levels of one-to-one marketing effectiveness. We discuss the strengths and challenges of using the propensity score approach to design and execute CRM related observational studies. We also discuss the applicability of the framework in this paper to study typical causal questions in business and electronic commerce research at the firm, individual and economy levels, and to clarify the assumptions that researchers must make to infer causality from observational data.

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