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Methods to adjust for multiple comparisons in the analysis and sample size calculation of randomised controlled trials with multiple primary outcomes
by
Omar, Rumana Z.
, Ambler, Gareth
, Vickerstaff, Victoria
in
Algorithms
/ Clinical trials
/ Computer Simulation
/ Data analysis
/ Data Interpretation, Statistical
/ Health Sciences
/ Humans
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Methods
/ Models, Theoretical
/ Multiple comparison methods
/ Multiple outcome
/ Outcome Assessment, Health Care - methods
/ Outcome Assessment, Health Care - statistics & numerical data
/ Randomised controlled trials
/ Randomized Controlled Trials as Topic - methods
/ Randomized Controlled Trials as Topic - statistics & numerical data
/ Research Article
/ Sample Size
/ Sampling (Statistics)
/ Statistical analysis
/ Statistical Theory and Methods
/ Statistics
/ statistics and modelling
/ Statistics for Life Sciences
/ Theory of Medicine/Bioethics
/ Treatment outcome
2019
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Methods to adjust for multiple comparisons in the analysis and sample size calculation of randomised controlled trials with multiple primary outcomes
by
Omar, Rumana Z.
, Ambler, Gareth
, Vickerstaff, Victoria
in
Algorithms
/ Clinical trials
/ Computer Simulation
/ Data analysis
/ Data Interpretation, Statistical
/ Health Sciences
/ Humans
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Methods
/ Models, Theoretical
/ Multiple comparison methods
/ Multiple outcome
/ Outcome Assessment, Health Care - methods
/ Outcome Assessment, Health Care - statistics & numerical data
/ Randomised controlled trials
/ Randomized Controlled Trials as Topic - methods
/ Randomized Controlled Trials as Topic - statistics & numerical data
/ Research Article
/ Sample Size
/ Sampling (Statistics)
/ Statistical analysis
/ Statistical Theory and Methods
/ Statistics
/ statistics and modelling
/ Statistics for Life Sciences
/ Theory of Medicine/Bioethics
/ Treatment outcome
2019
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Methods to adjust for multiple comparisons in the analysis and sample size calculation of randomised controlled trials with multiple primary outcomes
by
Omar, Rumana Z.
, Ambler, Gareth
, Vickerstaff, Victoria
in
Algorithms
/ Clinical trials
/ Computer Simulation
/ Data analysis
/ Data Interpretation, Statistical
/ Health Sciences
/ Humans
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Methods
/ Models, Theoretical
/ Multiple comparison methods
/ Multiple outcome
/ Outcome Assessment, Health Care - methods
/ Outcome Assessment, Health Care - statistics & numerical data
/ Randomised controlled trials
/ Randomized Controlled Trials as Topic - methods
/ Randomized Controlled Trials as Topic - statistics & numerical data
/ Research Article
/ Sample Size
/ Sampling (Statistics)
/ Statistical analysis
/ Statistical Theory and Methods
/ Statistics
/ statistics and modelling
/ Statistics for Life Sciences
/ Theory of Medicine/Bioethics
/ Treatment outcome
2019
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Methods to adjust for multiple comparisons in the analysis and sample size calculation of randomised controlled trials with multiple primary outcomes
Journal Article
Methods to adjust for multiple comparisons in the analysis and sample size calculation of randomised controlled trials with multiple primary outcomes
2019
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Overview
Background
Multiple primary outcomes may be specified in randomised controlled trials (RCTs). When analysing multiple outcomes it’s important to control the family wise error rate (FWER). A popular approach to do this is to adjust the
p
-values corresponding to each statistical test used to investigate the intervention effects by using the Bonferroni correction. It’s also important to consider the power of the trial to detect true intervention effects. In the context of multiple outcomes, depending on the clinical objective, the power can be defined as:
‘disjunctive power’
, the probability of detecting at least one true intervention effect across all the outcomes or ‘
marginal power’
the probability of finding a true intervention effect on a nominated outcome.
We provide practical recommendations on which method may be used to adjust for multiple comparisons in the sample size calculation and the analysis of RCTs with multiple primary outcomes. We also discuss the implications on the sample size for obtaining 90% disjunctive power and 90% marginal power.
Methods
We use simulation studies to investigate the disjunctive power, marginal power and FWER obtained after applying Bonferroni, Holm, Hochberg, Dubey/Armitage-Parmar and Stepdown-minP adjustment methods. Different simulation scenarios were constructed by varying the number of outcomes, degree of correlation between the outcomes, intervention effect sizes and proportion of missing data.
Results
The Bonferroni and Holm methods provide the same disjunctive power. The Hochberg and Hommel methods provide power gains for the analysis, albeit small, in comparison to the Bonferroni method. The Stepdown-minP procedure performs well for complete data. However, it removes participants with missing values prior to the analysis resulting in a loss of power when there are missing data. The sample size requirement to achieve the desired disjunctive power may be smaller than that required to achieve the desired marginal power. The choice between whether to specify a disjunctive or marginal power should depend on the clincial objective.
Publisher
BioMed Central,BioMed Central Ltd,BMC
Subject
/ Data Interpretation, Statistical
/ Humans
/ Medicine
/ Methods
/ Outcome Assessment, Health Care - methods
/ Outcome Assessment, Health Care - statistics & numerical data
/ Randomised controlled trials
/ Randomized Controlled Trials as Topic - methods
/ Randomized Controlled Trials as Topic - statistics & numerical data
/ Statistical Theory and Methods
/ Statistics for Life Sciences
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