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Estimating Causal Treatment Effects in Placebo-Controlled Randomized Clinical Trials When High Placebo Response is Anticipated

Abstract

In placebo-controlled randomized clinical trials (RCTs), the placebo response significantly modifies treatment effects and diminishes the intention-to-treat (ITT) treatment effect, ΔITT. This study presents a novel two-stage framework for estimating the standardized causal treatment effect, ΔSTD, among the ITT population, under the assumption that their placebo responses are similar to the levels of self-administering medication at home. The first stage employs a real-world, pragmatic, single-blinded placebo lead-in to measure placebo responses to levels expected during routine at-home use. This is achieved by preserving the participants' expectations and controlling for trial-related factors that inflate the responses. In the second stage, a double-blinded randomized phase is used to estimate the conditional average treatment effect (CATE) as a function of placebo response levels and other important effect modifiers. To facilitate CATE estimation, the prognostic scores, defined as the expected placebo responses, are used for dimension reduction. The causal estimand ΔSTD is computed by integrating the CATE function over the distribution of the expected placebo response levels from stage one and other modifiers. We further derive theoretical values for ΔITT−ΔSTD to quantify the underestimated treatment benefit due to high placebo responses. The validity and statistical performance of the proposed framework are evaluated through comprehensive simulations.

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BibTeX
@misc{song2026estimating,
  title = {{Estimating Causal Treatment Effects in Placebo-Controlled Randomized Clinical Trials When High Placebo Response is Anticipated}},
  author = {Yang Song and Yunzhe Qian and Chanmin Kim and Gheorghe Doros},
  howpublished = {arXiv},
  year = {2026},
  month = oct,
  doi = {10.48550/arxiv.2609.09377},
  eprint = {2609.09377},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2609.09377},
}
RIS
TY  - UNPB
TI  - Estimating Causal Treatment Effects in Placebo-Controlled Randomized Clinical Trials When High Placebo Response is Anticipated
AU  - Yang Song
AU  - Yunzhe Qian
AU  - Chanmin Kim
AU  - Gheorghe Doros
PY  - 2026
DA  - 2026/10/14
PB  - arXiv
DO  - 10.48550/arxiv.2609.09377
UR  - https://arxiv.org/abs/2609.09377
AB  - In placebo-controlled randomized clinical trials (RCTs), the placebo response significantly modifies treatment effects and diminishes the intention-to-treat (ITT) treatment effect, Δ_ITT. This study presents a novel two-stage framework for estimating the standardized causal treatment effect, Δ_STD, among the ITT population, under the assumption that their placebo responses are similar to the levels of self-administering medication at home. The first stage employs a real-world, pragmatic, single-blinded placebo lead-in to measure placebo responses to levels expected during routine at-home use. This is achieved by preserving the participants' expectations and controlling for trial-related factors that inflate the responses. In the second stage, a double-blinded randomized phase is used to estimate the conditional average treatment effect (CATE) as a function of placebo response levels and other important effect modifiers. To facilitate CATE estimation, the prognostic scores, defined as the expected placebo responses, are used for dimension reduction. The causal estimand Δ_STD is computed by integrating the CATE function over the distribution of the expected placebo response levels from stage one and other modifiers. We further derive theoretical values for Δ_ITT−Δ_STD to quantify the underestimated treatment benefit due to high placebo responses. The validity and statistical performance of the proposed framework are evaluated through comprehensive simulations.
ER  -