<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(2)</volume><submitter>Wang B</submitter><pubmed_abstract>In 2019, the World Health Organization identified dengue as one of the top 10 global health threats. For the control of dengue, the Applying Wolbachia to Eliminate Dengue (AWED) study group conducted a cluster-randomized trial in Yogyakarta, Indonesia, and used a novel design, called the cluster-randomized test-negative design (CR-TND). This design can yield valid statistical inference with data collected by a passive surveillance system and thus has the advantage of cost-efficiency compared to traditional cluster-randomized trials. We investigate the statistical assumptions and properties of CR-TND under a randomization inference framework, which is known to be robust for small-sample problems. We find that, when the differential healthcare-seeking behavior comparing intervention and control varies across clusters (in contrast to the setting of Dufault and Jewell (Stat. Med.39 (2020a) 1429-1439) where the differential healthcare-seeking behavior is constant across clusters), current analysis methods for CR-TND can be biased and have inflated type I error. We propose the log-contrast estimator that can eliminate such bias and improve precision by adjusting for covariates. Furthermore, we extend our methods to handle partial intervention compliance and a stepped-wedge design, both of which appear frequently in cluster-randomized trials. Finally, we demonstrate our results by simulation studies and reanalysis of the AWED study.</pubmed_abstract><journal>The annals of applied statistics</journal><pagination>1592-1614</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12374749</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>RANDOMIZATION INFERENCE FOR CLUSTER-RANDOMIZED TEST-NEGATIVE DESIGNS WITH APPLICATION TO DENGUE STUDIES: UNBIASED ESTIMATION, PARTIAL COMPLIANCE, AND STEPPED-WEDGE DESIGN.</pubmed_title><pmcid>PMC12374749</pmcid><pubmed_authors>Dufault SM</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Jewell NP</pubmed_authors><pubmed_authors>Small DS</pubmed_authors></additional><is_claimable>false</is_claimable><name>RANDOMIZATION INFERENCE FOR CLUSTER-RANDOMIZED TEST-NEGATIVE DESIGNS WITH APPLICATION TO DENGUE STUDIES: UNBIASED ESTIMATION, PARTIAL COMPLIANCE, AND STEPPED-WEDGE DESIGN.</name><description>In 2019, the World Health Organization identified dengue as one of the top 10 global health threats. For the control of dengue, the Applying Wolbachia to Eliminate Dengue (AWED) study group conducted a cluster-randomized trial in Yogyakarta, Indonesia, and used a novel design, called the cluster-randomized test-negative design (CR-TND). This design can yield valid statistical inference with data collected by a passive surveillance system and thus has the advantage of cost-efficiency compared to traditional cluster-randomized trials. We investigate the statistical assumptions and properties of CR-TND under a randomization inference framework, which is known to be robust for small-sample problems. We find that, when the differential healthcare-seeking behavior comparing intervention and control varies across clusters (in contrast to the setting of Dufault and Jewell (Stat. Med.39 (2020a) 1429-1439) where the differential healthcare-seeking behavior is constant across clusters), current analysis methods for CR-TND can be biased and have inflated type I error. We propose the log-contrast estimator that can eliminate such bias and improve precision by adjusting for covariates. Furthermore, we extend our methods to handle partial intervention compliance and a stepped-wedge design, both of which appear frequently in cluster-randomized trials. Finally, we demonstrate our results by simulation studies and reanalysis of the AWED study.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2026-04-08T10:03:11.282Z</modification><creation>2026-04-08T01:11:09.022Z</creation></dates><accession>S-EPMC12374749</accession><cross_references><pubmed>40855892</pubmed><doi>10.1214/22-aoas1684</doi></cross_references></HashMap>