Evidence map›Paper›PMID 41964891›Full record

ArticleJournal of patient-reported outcomes2026

Missing data considerations for patient reported outcome measures in randomized controlled trials.

Fan Wang, Shenran Deng, Jing Sun, Cunjie Lin, Shuping Jiang, Josephine M Norquist, Gregory T Golm, Jiaxin Xie, Yanfen Guan, William W B Wang and 3 more

Abstract read
In one paragraph

Article in Journal of patient-reported outcomes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Fan Wang *Biostatistics and Research Decision Sciences, MSD China, Beijing, China.
Shenran Deng *Center for Applied Statistics, School of Statistics, Institute of Health Data Science, Renmin University of China, Beijing, China.
Jing SunCenter for Applied Statistics, School of Statistics, Institute of Health Data Science, Renmin University of China, Beijing, China.
Cunjie LinCenter for Applied Statistics, School of Statistics, Institute of Health Data Science, Renmin University of China, Beijing, China.
Shuping JiangBiostatistics and Research Decision Sciences, MSD China, Beijing, China.
Josephine M NorquistBiostatistics and Research Decision Sciences, Patient-Centered Endpoints and Strategy, Merck & Co. Inc., Rahway, NJ, USA.
Gregory T GolmBiostatistics and Research Decision Sciences, Late Development Statistics, Merck & Co. Inc, Rahway, NJ, USA.
Jiaxin XieCenter for Applied Statistics, School of Statistics, Institute of Health Data Science, Renmin University of China, Beijing, China.
Yanfen GuanBiostatistics and Research Decision Sciences, Patient-Centered Endpoints and Strategy, Merck & Co. Inc., Rahway, NJ, USA.
William W B WangBiostatistics and Research Decision Sciences, Late Development Statistics, Merck & Co. Inc, Rahway, NJ, USA.
Lianzhe XuBiostatistics and Research Decision Sciences, Late Development Statistics, Merck & Co. Inc, Rahway, NJ, USA.
Hao MeiCenter for Applied Statistics, School of Statistics, Institute of Health Data Science, Renmin University of China, Beijing, China. hao.mei@ruc.edu.cn.ORCID http://orcid.org/0000-0002-1083-9542
Yang LiCenter for Applied Statistics, School of Statistics, Institute of Health Data Science, Renmin University of China, Beijing, China.

Funding

Humanities and Social Science Fund of Ministry of Education of China 22JJD910001
6 · The paper itself

Abstract

backgroundPatient-reported outcome (PRO) measures are widely used in clinical trials to capture patients’ perspectives on their health and treatment. However, missing data remains a major challenge and can lead to biased or incomplete results. Understanding how different methods for handling missing data perform under realistic conditions is essential for decision-making.

methodsWe conducted a simulation study informed by a review of 87 PRO instruments, modeling both simple and complex questionnaire structures in a hypothetical randomized trial. Under both the missing at random (MAR) and missing not at random (MNAR) assumptions, four commonly used approaches were evaluated: multiple imputation (MI) at the item level, MI at the total score level, item mean, and mixed model for repeated measurements (MMRM). To make the study more realistic, we also ran simulations using actual trial data from the COU-AA-302 study, focusing on the Functional Assessment of Cancer Therapy–Prostate (FACT-P) questionnaire.

resultsThe simulation results supported the use of the “Half Rule” under MAR. When the number of missing items did not exceed half of the total items, item mean imputation showed reasonable estimation with low root mean squared error, high power, and low type 1 error. MI on item scores consistently performed well, but inflated type 1 error under certain MNAR scenarios. As the missing visit rate increased, the advantage of item level imputation diminished, i.e., RMSE approached and eventually exceeded that of MI on the total score. In the trial data analysis, given the high missing visit rate in the collected FACT-P data, MI on total score level performed not worse than MI on item score level.

conclusionsNo single method is optimal for all situations. Item-level imputation performs well when missing data are minimal and occur at random, but it becomes less reliable when data is missing not at random. For complex PROs or studies with many missing visits, imputing at the total score level with the “Half Rule” offers a practical alternative. Strategies should match the missingness pattern, supported by simulations and sensitivity analyses to ensure robust results.

Indexed as

Patient Reported Outcome MeasuresRandomized Controlled Trials as TopicComputer SimulationData Interpretation, StatisticalHumansMaleModels, StatisticalResearch DesignSurveys and QuestionnairesClinical trialsLongitudinal analysisMissing dataMultiple imputationPatient-reported outcomes

Identifiers

PMID41964891
PMCPMC13194809

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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.