Evidence map›Paper›PMID 40000941›Full record

ArticleBMC medical research methodology2025

Accounting for extent of non-compliance when estimating treatment effects on an ordinal outcome in randomized clinical trials.

Junxian Zhu, Jialiang Li, A Mark Richards, Mark Y Chan, Bee-Choo Tai

Abstract read
In one paragraph

Article in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Junxian ZhuSaw Swee Hock School of Public Health, National University of Singapore, 21 Lower Kent Ridge Road, Singapore, 119077, Singapore.
Jialiang LiDepartment of Statistics and Data Science, National University of Singapore, 21 Lower Kent Ridge Road, Singapore, 119077, Singapore.
A Mark RichardsCardiovascular Research Institute, Yong Loo-Lin School of Medicine, National University of Singapore, 21 Lower Kent Ridge Road, Singapore, 119077, Singapore.
Mark Y ChanCardiovascular Research Institute, Yong Loo-Lin School of Medicine, National University of Singapore, 21 Lower Kent Ridge Road, Singapore, 119077, Singapore.
Bee-Choo TaiSaw Swee Hock School of Public Health, National University of Singapore, 21 Lower Kent Ridge Road, Singapore, 119077, Singapore. ephtbc@nus.edu.sg.

Funding

National University Health System, Singapore NUHSRO/2020/144/RO5+6/Seed-Sep/04
6 · The paper itself

Abstract

backgroundIn randomized clinical trials (RCTs) with non-compliance, evaluating the causal effects of interventions would lead to a more precise estimation of treatment effect when the estimand of interest is the effect of treatment amongst compliers. While there is a large body of literature addressing the issue of non-compliance for continuous, binary, and time-to-event outcomes, this issue is seldom discussed for ordinal outcomes.

methodsIn this paper, we consider one-sided non-compliance. We introduce an extension of the inverse probability weighting (IPW) method for handling non-compliance involving an ordinal outcome by fully utilizing the information of non-compliance and defining it as a categorical variable to describe the extent of non-compliance. This is in contrast to the usual convention where compliance is regarded as a binary variable. We provide the identification and asymptotic distribution of the proposed method. We compare the proposed method (IPW_Dnew) with intention-to-treat (ITT), per protocol (PP), instrumental variable (IV), and IPW method via a simulation study and real-life data from the JOBS II intervention trial and the IMMACULATE trial.

resultsSimulation results demonstrate that the proposed method performs better than other methods in terms of bias, coverage, mean squared error, power and Type I error under various scenarios, particularly in situations with selection bias and partial compliance. In the empirical study, a substantial estimate of partial compliance by IPW_Dnew implies that there may be a partial compliance effect.

conclusionFor ordinal outcome in the presence of non-compliance, we suggest using the proposed method to estimate the causal effect of treatment amongst compliers and partial compliers, especially when there exists selection bias.

Indexed as

Patient ComplianceRandomized Controlled Trials as TopicComputer SimulationData Interpretation, StatisticalHumansModels, StatisticalTreatment OutcomeInverse probability weightingNon-complianceOrdinal outcomeRandomized clinical trialSelection bias

Identifiers

PMID40000941
PMCPMC11852586

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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.