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Uncovering treatment effect heterogeneity in pragmatic gerontology trials
Changjun Li1, Heather Allore2, Michael O Harhay3
1Department of Biostatistics, Yale School of Public Health, New Haven, CT, USA; Cardiovascular Medicine Analytics Center, Yale School of Medicine, New Haven, CT, USA; Center for Methods in Implementation and Prevention Science, Yale School of Public Health, New Haven, CT, USA.
Abstract:
Detecting heterogeneity in treatment response enriches the interpretation of gerontologic trials. In aging research, estimating the intervention's effect on clinically meaningful outcomes poses analytical challenges when outcomes are truncated by death. For example, in the Whole Systems Demonstrator trial, a large cluster-randomized study evaluating telecare among older adults, the overall effect of the intervention on quality of life was found to be null. However, this marginal intervention estimate obscures potential heterogeneity of individuals responding to the intervention, particularly among those who survive to the end of follow-up. To explore this heterogeneity, we adopt a causal framework grounded in principal stratification, targeting the Survivor Average Causal Effect (SACE)-the treatment effect among "always-survivors," or those who would survive regardless of treatment assignment. We extend this framework using Bayesian Additive Regression Trees (BART), a nonparametric machine learning method, to flexibly model both latent principal strata and stratum-specific potential outcomes. This enables the estimation of the Conditional SACE (CSACE), allowing us to uncover variation in treatment effects across subgroups defined by baseline characteristics. Our analysis reveals that despite the null average effect, some subgroups experience distinct quality of life benefits (or lack thereof) from telecare, highlighting opportunities for more personalized intervention strategies. This study demonstrates how embedding machine learning methods, such as BART, within a principled causal inference framework can offer deeper insights into trial data with complex features including truncation by death and clustering-key considerations in analyzing pragmatic gerontology trials.
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