Literature DB >> 28074483

Sample size calculations for randomised trials including both independent and paired data.

Lisa N Yelland1,2, Thomas R Sullivan1, David J Price3, Katherine J Lee4,5.   

Abstract

Randomised trials including a mixture of independent and paired data arise in many areas of health research, yet methods for determining the sample size for such trials are lacking. We derive design effects algebraically assuming clustering because of paired data will be taken into account in the analysis using generalised estimating equations with either an independence or exchangeable working correlation structure. Continuous and binary outcomes are considered, along with three different methods of randomisation: cluster randomisation, individual randomisation and randomisation to opposite treatment groups. The design effect is shown to depend on the intracluster correlation coefficient, proportion of observations belonging to a pair, working correlation structure, type of outcome and method of randomisation. The derived design effects are validated through simulation and example calculations are presented to illustrate their use in sample size planning. These design effects will enable appropriate sample size calculations to be performed for future randomised trials including both independent and paired data.
Copyright © 2017 John Wiley & Sons, Ltd. Copyright © 2017 John Wiley & Sons, Ltd.

Keywords:  clustered data; design effect; generalised estimating equations; sample size

Mesh:

Year:  2017        PMID: 28074483     DOI: 10.1002/sim.7201

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  3 in total

1.  Correlation between neonatal outcomes of twins depends on the outcome: secondary analysis of twelve randomised controlled trials.

Authors:  L N Yelland; E Schuit; J Zamora; P F Middleton; A C Lim; A H Nassar; L Rode; V Serra; E A Thom; C Vayssière; Bwj Mol; S Gates
Journal:  BJOG       Date:  2018-06-25       Impact factor: 6.531

2.  Protocol for assessing if behavioural functioning of infants born <29 weeks' gestation is improved by omega-3 long-chain polyunsaturated fatty acids: follow-up of a randomised controlled trial.

Authors:  Jacqueline F Gould; Rachel M Roberts; Peter J Anderson; Maria Makrides; Thomas R Sullivan; Robert A Gibson; Andrew J McPhee; Lex William Doyle; Gillian Opie; Javeed Travadi; Jeanie L Y Cheong; Peter G Davis; Mary Sharp; Karen Simmer; Kenneth Tan; Scott Morris; Kei Lui; Srinivas Bolisetty; Helen Liley; Jacqueline Stack; Karen P Best; Carmel T Collins
Journal:  BMJ Open       Date:  2021-05-05       Impact factor: 2.692

3.  Protocol for assessing whether cognition of preterm infants <29 weeks' gestation can be improved by an intervention with the omega-3 long-chain polyunsaturated fatty acid docosahexaenoic acid (DHA): a follow-up of a randomised controlled trial.

Authors:  Jacqueline F Gould; Maria Makrides; Thomas R Sullivan; Peter J Anderson; Robert A Gibson; Karen P Best; Andrew J McPhee; Lex William Doyle; Gillian Opie; Javeed Travadi; Jeanie Cheong; Peter G Davis; Mary Sharp; Karen Simmer; Carmel T Collins
Journal:  BMJ Open       Date:  2021-02-05       Impact factor: 2.692

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.