Evidence map›Paper›PMID 41118457›Full record

ArticleStatistical methods in medical research2025

Center-specific causal inference with multicenter trials-Interpreting trial evidence in the context of each participating center.

Sarah E Robertson, Jon A Steingrimsson, Nina R Joyce, Elizabeth A Stuart, Issa J Dahabreh

Abstract read
In one paragraph

Article in Statistical methods in medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
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

5 authors.

Sarah E RobertsonCAUSALab, Harvard T.H. Chan School of Public Health, Boston, MA, USA.ORCID 0000-0002-8973-8655
Jon A SteingrimssonDepartment of Biostatistics, Brown University School of Public Health, Providence, RI, USA.
Nina R JoyceDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA.
Elizabeth A StuartDepartments of Mental Health, Biostatistics, and Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Issa J DahabrehCAUSALab, Harvard T.H. Chan School of Public Health, Boston, MA, USA.ORCID 0000-0002-2215-9931

Funding

Methods for generalizing inferences from cluster randomized controlled trials to target populationsR01LM013616 · NLM · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI DAHABREH, ISSA J. · 2022 to 2025
$1.4M
Learning about the effectiveness of lung cancer screening in real-world target populationsK99CA287059 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI ROBERTSON, SARAH E · 2024 to 2025
$258k
AHRQ HHS R36 HS028373NCI NIH HHS K99 CA287059NLM NIH HHS R01 LM013616
6 · The paper itself

Abstract

In multicenter randomized trials, when effect modifiers have a different distribution across centers, comparisons between treatment groups that average (standardize) effects over centers may not apply to any of the populations underlying the individual centers. In the presence of such heterogeneity, interpreting the evidence produced by a multicenter trial in the context of the local population underlying each center may be necessary. Here, we identify center-specific effects under conditions that are largely supported by the study design and are weaker than those underlying popular methods for the analysis of multicenter studies, in the presence of associations between center membership and the outcome ("center-outcome associations" conditional on baseline covariates and treatment). We then consider an additional testable condition of "no center-outcome associations," given baseline covariates and treatment. We propose methods for estimating center-specific average treatment effects, when center-outcome associations are present and when they are absent. When center-outcome associations are absent, we discuss how the proposed methods are often more efficient and make weaker conditions than related transportability methods applied to multicenter trials. We evaluate the performance of the methods in a simulation study and illustrate their implementation using data from the Hepatitis C Antiviral Long-Term Treatment Against Cirrhosis trial.

Indexed as

CausalityMulticenter Studies as TopicRandomized Controlled Trials as TopicComputer SimulationData Interpretation, StatisticalHumansModels, StatisticalResearch Designcausal inferencegeneralizabilityheterogeneityMulticenter trialtransportability

Identifiers

PMID41118457
PMCPMC12869369

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.