Modern Causal Inference Approaches to Improve Power for Subgroup Analysis in Randomized Controlled Trials

Fuente: arXiv
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Main Authors: D'Alessandro, Antonio, Kim, Jiyu, Adhikari, Samrachana, Goff, Donald, Stoffi, Falco J. Bargagli, Santacatterina, Michele
Format: Preprint
Published: 2025
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author D'Alessandro, Antonio
Kim, Jiyu
Adhikari, Samrachana
Goff, Donald
Stoffi, Falco J. Bargagli
Santacatterina, Michele
author_facet D'Alessandro, Antonio
Kim, Jiyu
Adhikari, Samrachana
Goff, Donald
Stoffi, Falco J. Bargagli
Santacatterina, Michele
contents Randomized controlled trials (RCTs) often include subgroup analyses to assess whether treatment effects vary across pre-specified patient populations. However, these analyses frequently suffer from small sample sizes which limit the power to detect heterogeneous effects. Power can be improved by leveraging predictors of the outcome -- i.e., through covariate adjustment -- as well as by borrowing external data from similar RCTs or observational studies. The benefits of covariate adjustment may be limited when the trial sample is small. Borrowing external data can increase the effective sample size and improve power, but it introduces two key challenges: (i) integrating data across sources can lead to model misspecification, and (ii) practical violations of the positivity assumption -- where the probability of receiving the target treatment is near-zero for some covariate profiles in the external data -- can lead to extreme inverse-probability weights and unstable inferences, ultimately negating potential power gains. To account for these shortcomings, we present an approach to improving power in pre-planned subgroup analyses of small RCTs that leverages both baseline predictors and external data. We propose debiased estimators that accommodate parametric, machine learning, and nonparametric Bayesian methods. To address practical positivity violations, we introduce three estimators: a covariate-balancing approach, an automated debiased machine learning (DML) estimator, and a calibrated DML estimator. We show improved power in various simulations and offer practical recommendations for the application of the proposed methods. Finally, we apply them to evaluate the effectiveness of citalopram for negative symptoms in first-episode schizophrenia patients across subgroups defined by duration of untreated psychosis, using data from two small RCTs.
format Preprint
id arxiv_https___arxiv_org_abs_2505_08960
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Modern Causal Inference Approaches to Improve Power for Subgroup Analysis in Randomized Controlled Trials
D'Alessandro, Antonio
Kim, Jiyu
Adhikari, Samrachana
Goff, Donald
Stoffi, Falco J. Bargagli
Santacatterina, Michele
Methodology
62P10
Randomized controlled trials (RCTs) often include subgroup analyses to assess whether treatment effects vary across pre-specified patient populations. However, these analyses frequently suffer from small sample sizes which limit the power to detect heterogeneous effects. Power can be improved by leveraging predictors of the outcome -- i.e., through covariate adjustment -- as well as by borrowing external data from similar RCTs or observational studies. The benefits of covariate adjustment may be limited when the trial sample is small. Borrowing external data can increase the effective sample size and improve power, but it introduces two key challenges: (i) integrating data across sources can lead to model misspecification, and (ii) practical violations of the positivity assumption -- where the probability of receiving the target treatment is near-zero for some covariate profiles in the external data -- can lead to extreme inverse-probability weights and unstable inferences, ultimately negating potential power gains. To account for these shortcomings, we present an approach to improving power in pre-planned subgroup analyses of small RCTs that leverages both baseline predictors and external data. We propose debiased estimators that accommodate parametric, machine learning, and nonparametric Bayesian methods. To address practical positivity violations, we introduce three estimators: a covariate-balancing approach, an automated debiased machine learning (DML) estimator, and a calibrated DML estimator. We show improved power in various simulations and offer practical recommendations for the application of the proposed methods. Finally, we apply them to evaluate the effectiveness of citalopram for negative symptoms in first-episode schizophrenia patients across subgroups defined by duration of untreated psychosis, using data from two small RCTs.
title Modern Causal Inference Approaches to Improve Power for Subgroup Analysis in Randomized Controlled Trials
topic Methodology
62P10
url https://arxiv.org/abs/2505.08960