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Causal Identification for Complex Functional Longitudinal Studies
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Proposes a nonparametric causal identification framework for functional longitudinal data with time-varying outcomes, mortality and censoring, generalizing g-computation, IPW, and doubly robust formulas, and checks g-computation with Gaussian-process Monte Carlo simulations.
Problem
Causal identification of marginal mean counterfactual outcomes when treatments, confounders and outcomes are continuous-time functional processes, creating uncountably infinite treatment-confounder feedback and infinite-dimensional data, with death and censoring.
Approach
Extends the coarsened-data framework and stochastic process/measure theory to continuous time: partitions of time with treatment intervened to a stochastic regime G converge in total variation to a target distribution, yielding g-computation, IPW and doubly robust identification formulas that are shown to impose no restrictions on observed data.
Key results
- Monte Carlo g-computation approximations converge toward the analytical target value 0 as sample size n (100 to 2500) increases, with reduced variance.
- Increasing grid size K (10, 50, 250) alone does not consistently improve accuracy or reduce variance, whereas increasing both n and K does.
- The identification is shown to be nonparametric: the set of identifiable observed-data distributions is dense in total variation norm.
Measured effects reported in the paper
| What was changed | Where | Measured | Effect |
|---|---|---|---|
| increase sample size while holding grid size fixed | g-computation formula · Monte Carlo simulation (K = 10, 50, 250; n = 100, 500, 2500) | approximation accuracy | Helped |
| increase sample size while holding grid size fixed | g-computation formula · Monte Carlo simulation (K = 10, 50, 250; n = 100, 500, 2500) | variance | Helped |
| increase grid size while holding sample size fixed | g-computation formula · Monte Carlo simulation (K = 10, 50, 250; n = 100, 500, 2500) | approximation accuracy | Mixed |
| increase grid size while holding sample size fixed | g-computation formula · Monte Carlo simulation (K = 10, 50, 250; n = 100, 500, 2500) | variance | Mixed |
| increase both sample size and grid size | g-computation formula · Monte Carlo simulation (K = 10, 50, 250; n = 100, 500, 2500) | approximation accuracy | Helped |
| increase both sample size and grid size | g-computation formula · Monte Carlo simulation (K = 10, 50, 250; n = 100, 500, 2500) | variance | Helped |
Surprising findings
- Refining the time grid alone does not consistently improve approximation accuracy or variance in the simulations.
Limitations
- Only population-level identification; no estimation or inference, and no sample-level (sparse/irregular) data analysis.
- IPW and doubly robust formulas are not numerically evaluated since they cannot be directly approximated without estimation.
- Nonparametric claim is 'almost' nonparametric, relying on a piecewise continuous path-space regularity condition.
Experimental setup
Datasets: simulated Gaussian process data (glucose/insulin-style outcome and treatment)
Metrics: bias of g-computation approximation boxplot spread across 10,000 repeats
Builds on: coarsened data framework g-computation formula inverse probability weighting doubly robust formula
Closest papers by meaning
- Composable Causality: A Toolkit for Systematic Time-Series Causal Discovery and Treatment-Effect Benchmarking (NeurIPS 2026 · similarity 0.88)
- Temporal Causal Mediation through a Point Process: Direct and Indirect Effects of Healthcare Interventions (NeurIPS 2023 · similarity 0.88)
- Instrumental Variable Estimation for Causal Inference in Longitudinal Data with Time-Dependent Latent Confounders (AAAI 2024 · similarity 0.86)
- Data-Driven Covariate Selection for Nonparametric and Cycle-Agnostic Causal Effect Estimation (NeurIPS 2026 · similarity 0.86)
- Local Learning for Covariate Selection in Nonparametric Causal Effect Estimation with Latent Variables (NeurIPS 2025 · similarity 0.85)
- Causal Attribution Analysis for Continuous Outcomes (ICML 2025 · similarity 0.85)
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