跳到正文
← 返回论文列表与筛选
阅读说明

本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

本页为预印本版本;arXiv 收录、作者填写的期刊信息以及作者既有发表经历,都不单独证明本篇已接收。作者发表记录按 OpenAlex 身份与完整姓名、本站覆盖期刊 ISSN 及正式卷期核对,只展示已核实例,档案仍可能误合并。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。

分类依据与纠错

AI 根据所提供的论文材料归类:摘要直接讨论随机试验中的因果效应、因果模型与 TMLE 估计。

反馈分类问题

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Joshua Nugent
Elijah Kakande
Gabriel Chamie
Jane Kabami
Diane V. Havlir
Moses Kamya
Laura Balzer

部分聚类随机试验中的因果推断

研究问题
当干预组存在组内依赖、对照组个体独立时,不同随机化设计如何影响因果效应估计,并如何利用协变量提高推断效率?
方法与思路
作者用非参数因果模型描述三类试验的数据生成与依赖结构,并为部分聚类设计提出结合协变量调整和机器学习的 TMLE 实现。
材料陈述的贡献
摘要称,两种部分聚类设计可共享依赖结构与统计方法;模拟报告功效表现,SEARCH-IPT 应用报告效率提升。
阅读关注点
应核对不同设计共享依赖结构的条件、因果目标与分析单位,以及 TMLE 如何处理组内依赖、协变量调整和方差估计。
阅读边界
这是 arXiv 预印本,同行评审或期刊接收未核实;摘要未说明模型稳健性的具体条件,效率提升也不能直接推广至其他试验。

原文摘要

Clustering and dependence are common in trials. For example, in some cluster randomized trials (CRTs), pre-existing clusters are enrolled, randomized, and serve as the basis of intervention delivery. Such CRTs are "fully clustered": participants are dependent within clusters. In contrast, "partially clustered" trials contain a mix of participants that are dependent within clusters and participants that are completely independent. One example of this design is a trial where participants are artificially grouped together for the purposes of randomization only; then, for intervention participants, the groups are the basis for intervention delivery, while control participants are un-grouped. Another example is an individually randomized group treatment trial (IRGTT) where participants are individually randomized and, post-randomization, intervention participants are grouped for intervention delivery, while the control participants remain un-grouped. For the three trial designs, we use causal models to non-parametrically describe the data generating process and formalize the observed data dependence structure. We show that despite the different randomization approach, both designs can be represented with the same dependence structure, enabling the use of the same statistical methods for estimation and inference of causal effects. We propose a novel implementation of targeted minimum loss-based estimation (TMLE) for these trials. TMLE is model-robust, leverages covariate adjustment and machine learning, and estimates many causal effects. In simulations, TMLE achieved comparable higher statistical power than alternatives for partially clustered designs. Finally, application to real data from the SEARCH-IPT trial resulted in 20-57% efficiency gains, demonstrating the consequences of our proposed approach.

笔记与分组