Evidence map›Paper›PMID 36609282›Full record

ArticleTrials2023

A comparison of covariate adjustment approaches under model misspecification in individually randomized trials.

Mia S Tackney, Tim Morris, Ian White, Clemence Leyrat, Karla Diaz-Ordaz, Elizabeth Williamson

Abstract read
In one paragraph

Article in Trials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  10. Model-based standardization using multiple imputation.BMC medical research methodology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Mia S TackneyDepartment of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK. Mia.Tackney@mrc-bsu.cam.ac.uk.ORCID http://orcid.org/0000-0003-3868-0550
Tim MorrisMRC Clinical Trials Unit at UCL, London, UK.
Ian WhiteMRC Clinical Trials Unit at UCL, London, UK.
Clemence LeyratDepartment of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.
Karla Diaz-OrdazDepartment of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.
Elizabeth WilliamsonDepartment of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.

Funding

Health Data Research UK N/AMedical Research Council MC_UU_00004/07Medical Research Council Programme MC_UU_00004/07MRC Network of Hubs for trials methodology research (MR/ L004933/2-N96)Royal Society-Wellcome Trust Sir Henry Dale fellowship 218554/Z/19/ZUK Medical Research Council MR/T032448/1Wellcome Trust
6 · The paper itself

Abstract

Adjustment for baseline covariates in randomized trials has been shown to lead to gains in power and can protect against chance imbalances in covariates. For continuous covariates, there is a risk that the the form of the relationship between the covariate and outcome is misspecified when taking an adjusted approach. Using a simulation study focusing on individually randomized trials with small sample sizes, we explore whether a range of adjustment methods are robust to misspecification, either in the covariate-outcome relationship or through an omitted covariate-treatment interaction. Specifically, we aim to identify potential settings where G-computation, inverse probability of treatment weighting (IPTW), augmented inverse probability of treatment weighting (AIPTW) and targeted maximum likelihood estimation (TMLE) offer improvement over the commonly used analysis of covariance (ANCOVA). Our simulations show that all adjustment methods are generally robust to model misspecification if adjusting for a few covariates, sample size is 100 or larger, and there are no covariate-treatment interactions. When there is a non-linear interaction of treatment with a skewed covariate and sample size is small, all adjustment methods can suffer from bias; however, methods that allow for interactions (such as G-computation with interaction and IPTW) show improved results compared to ANCOVA. When there are a high number of covariates to adjust for, ANCOVA retains good properties while other methods suffer from under- or over-coverage. An outstanding issue for G-computation, IPTW and AIPTW in small samples is that standard errors are underestimated; they should be used with caution without the availability of small-sample corrections, development of which is needed. These findings are relevant for covariate adjustment in interim analyses of larger trials.

Indexed as

Randomized Controlled Trials as TopicComputer SimulationHumansProbabilitySample SizeAIPTWANCOVACovariate adjustmentG-computationIPTWMisspecificationRandomized controlled trialsTMLE

Identifiers

PMID36609282
PMCPMC9817411

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.