Sample size and power considerations for cluster randomized trials with count outcomes subject to right truncation

Cluster randomized trials (CRTs) are widely used in epidemiological and public health studies assessing population‐level effect of group‐based interventions. One important application of CRTs is the control of vector‐borne disease, such as malaria. However, a particular challenge for designing these...

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Published inBiometrical journal Vol. 63; no. 5; pp. 1052 - 1071
Main Authors Li, Fan, Tong, Guangyu
Format Journal Article
LanguageEnglish
Published Germany Wiley - VCH Verlag GmbH & Co. KGaA 01.06.2021
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Abstract Cluster randomized trials (CRTs) are widely used in epidemiological and public health studies assessing population‐level effect of group‐based interventions. One important application of CRTs is the control of vector‐borne disease, such as malaria. However, a particular challenge for designing these trials is that the primary outcome involves counts of episodes that are subject to right truncation. While sample size formulas have been developed for CRTs with clustered counts, they are not directly applicable when the counts are right truncated. To address this limitation, we discuss two marginal modeling approaches for the analysis of CRTs with truncated counts and develop two corresponding closed‐form sample size formulas to facilitate the design of such trials. The proposed sample size formulas allow investigators to explore the power under a large number of scenarios without computationally intensive simulations. The proposed formulas are validated in extensive simulations. We further explore the implication of right truncation on power and apply the proposed formulas to illustrate the power calculation for a malaria control CRT where the primary outcome is subject to right truncation.
AbstractList Cluster randomized trials (CRTs) are widely used in epidemiological and public health studies assessing population‐level effect of group‐based interventions. One important application of CRTs is the control of vector‐borne disease, such as malaria. However, a particular challenge for designing these trials is that the primary outcome involves counts of episodes that are subject to right truncation. While sample size formulas have been developed for CRTs with clustered counts, they are not directly applicable when the counts are right truncated. To address this limitation, we discuss two marginal modeling approaches for the analysis of CRTs with truncated counts and develop two corresponding closed‐form sample size formulas to facilitate the design of such trials. The proposed sample size formulas allow investigators to explore the power under a large number of scenarios without computationally intensive simulations. The proposed formulas are validated in extensive simulations. We further explore the implication of right truncation on power and apply the proposed formulas to illustrate the power calculation for a malaria control CRT where the primary outcome is subject to right truncation.
Cluster randomized trials (CRTs) are widely used in epidemiological and public health studies assessing population‐level effect of group‐based interventions. One important application of CRTs is the control of vector‐borne disease, such as malaria. However, a particular challenge for designing these trials is that the primary outcome involves counts of episodes that are subject to right truncation. While sample size formulas have been developed for CRTs with clustered counts, they are not directly applicable when the counts are right truncated. To address this limitation, we discuss two marginal modeling approaches for the analysis of CRTs with truncated counts and develop two corresponding closed‐form sample size formulas to facilitate the design of such trials. The proposed sample size formulas allow investigators to explore the power under a large number of scenarios without computationally intensive simulations. The proposed formulas are validated in extensive simulations. We further explore the implication of right truncation on power and apply the proposed formulas to illustrate the power calculation for a malaria control CRT where the primary outcome is subject to right truncation.
Cluster randomized trials (CRTs) are widely used in epidemiological and public health studies assessing population-level effect of group-based interventions. One important application of CRTs is the control of vector-borne disease, such as malaria. However, a particular challenge for designing these trials is that the primary outcome involves counts of episodes that are subject to right truncation. While sample size formulas have been developed for CRTs with clustered counts, they are not directly applicable when the counts are right truncated. To address this limitation, we discuss two marginal modeling approaches for the analysis of CRTs with truncated counts and develop two corresponding closed-form sample size formulas to facilitate the design of such trials. The proposed sample size formulas allow investigators to explore the power under a large number of scenarios without computationally intensive simulations. The proposed formulas are validated in extensive simulations. We further explore the implication of right truncation on power and apply the proposed formulas to illustrate the power calculation for a malaria control CRT where the primary outcome is subject to right truncation.Cluster randomized trials (CRTs) are widely used in epidemiological and public health studies assessing population-level effect of group-based interventions. One important application of CRTs is the control of vector-borne disease, such as malaria. However, a particular challenge for designing these trials is that the primary outcome involves counts of episodes that are subject to right truncation. While sample size formulas have been developed for CRTs with clustered counts, they are not directly applicable when the counts are right truncated. To address this limitation, we discuss two marginal modeling approaches for the analysis of CRTs with truncated counts and develop two corresponding closed-form sample size formulas to facilitate the design of such trials. The proposed sample size formulas allow investigators to explore the power under a large number of scenarios without computationally intensive simulations. The proposed formulas are validated in extensive simulations. We further explore the implication of right truncation on power and apply the proposed formulas to illustrate the power calculation for a malaria control CRT where the primary outcome is subject to right truncation.
Author Li, Fan
Tong, Guangyu
AuthorAffiliation 3 Yale Center for Analytical Sciences, New Haven, CT, USA
1 Department of Biostatistics, Yale School of Public Health, New Haven, CT, USA
2 Center for Methods in Implementation and Prevention Science, Yale University, New Haven, CT, USA
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arm-specific exchangeable correlation
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Snippet Cluster randomized trials (CRTs) are widely used in epidemiological and public health studies assessing population‐level effect of group‐based interventions....
Cluster randomized trials (CRTs) are widely used in epidemiological and public health studies assessing population-level effect of group-based interventions....
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SubjectTerms arm‐specific exchangeable correlation
Cluster Analysis
Clusters
coefficient of variation
Disease control
Epidemiology
generalized estimating equations
group‐randomized trials
Malaria
Poisson distribution
Population studies
Public health
Randomized Controlled Trials as Topic
Research Design
Sample Size
unequal cluster sizes
Vector-borne diseases
Title Sample size and power considerations for cluster randomized trials with count outcomes subject to right truncation
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fbimj.202000230
https://www.ncbi.nlm.nih.gov/pubmed/33751620
https://www.proquest.com/docview/2536734702
https://www.proquest.com/docview/2504352410
https://pubmed.ncbi.nlm.nih.gov/PMC9132617
Volume 63
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