Clustered Encouragement Designs with Individual Noncompliance: Bayesian Inference with Randomization, and Application to Advance Directive Forms
DOI10.1093/BIOSTATISTICS/3.2.147zbMATH Open1134.62319OpenAlexW2111511840WikidataQ47670877 ScholiaQ47670877MaRDI QIDQ5701136FDOQ5701136
Authors: Constantine E. Frangakis, Donald B. Rubin, Xiao-Hua Zhou 
Publication date: 2 November 2005
Published in: Biostatistics (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1093/biostatistics/3.2.147
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ClusteringRubin causal modelCausal inferenceNoncomplianceAdvance directivePhenomenological Bayesian model
Bayesian inference (62F15) Applications of statistics to biology and medical sciences; meta analysis (62P10)
Cited In (18)
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- A mixed model approach to estimate the survivor average causal effect in cluster-randomized trials
- An Extended General Location Model for Causal Inferences from Data Subject to Noncompliance and Missing Values
- Designs in partially controlled studies: messages from a review
- Methods for clustered encouragement design studies with noncompliance and missing data
- A powerful and robust test statistic for randomization inference in group-randomized trials with matched pairs of groups
- Bounding the local average treatment effect in an instrumental variable analysis of engagement with a mobile intervention
- Bridging preference‐based instrumental variable studies and cluster‐randomized encouragement experiments: Study design, noncompliance, and average cluster effect ratio
- Multiple Imputation Methods for Treatment Noncompliance and Nonresponse in Randomized Clinical Trials
- Exploring Encouragement, Treatment, and Spillover Effects Using Principal Stratification, With Application to a Field Experiment on Teens’ Museum Attendance
- Estimating causal effects of treatment in RCTs with provider and subject noncompliance
- What are the statistical implications of treatment non-compliance in cluster randomized trials: a simulation study
- The essential role of pair matching in cluster-randomized experiments, with application to the Mexican Universal Health Insurance evaluation
- A Potential Outcomes Approach to Developmental Toxicity Analyses
- The potential for bias in principal causal effect estimation when treatment received depends on a key covariate
- Simple maximum likelihood estimates of efficacy in randomized trials and before-and-after studies, with implications for meta-analysis
- Designs in partially controlled studies: messages from a review
- Simple maximum likelihood estimates of efficacy in randomized trials and before-and-after studies, with implications for meta-analysis
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