Adaptive pair-matching in randomized trials with unbiased and efficient effect estimation

Stat Med. 2015 Mar 15;34(6):999-1011. doi: 10.1002/sim.6380. Epub 2014 Nov 25.

Abstract

In randomized trials, pair-matching is an intuitive design strategy to protect study validity and to potentially increase study power. In a common design, candidate units are identified, and their baseline characteristics used to create the best n/2 matched pairs. Within the resulting pairs, the intervention is randomized, and the outcomes measured at the end of follow-up. We consider this design to be adaptive, because the construction of the matched pairs depends on the baseline covariates of all candidate units. As a consequence, the observed data cannot be considered as n/2 independent, identically distributed pairs of units, as common practice assumes. Instead, the observed data consist of n dependent units. This paper explores the consequences of adaptive pair-matching in randomized trials for estimation of the average treatment effect, conditional the baseline covariates of the n study units. By avoiding estimation of the covariate distribution, estimators of this conditional effect will often be more precise than estimators of the marginal effect. We contrast the unadjusted estimator with targeted minimum loss based estimation and show substantial efficiency gains from matching and further gains with adjustment. This work is motivated by the Sustainable East Africa Research in Community Health study, an ongoing community randomized trial to evaluate the impact of immediate and streamlined antiretroviral therapy on HIV incidence in rural East Africa.

Keywords: adaptive designs; causal inference; efficiency; pair-matching; randomized trials; targeted minimum loss based estimation (TMLE).

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Africa
  • Anti-Retroviral Agents / therapeutic use
  • Cluster Analysis*
  • Computer Simulation
  • Data Interpretation, Statistical
  • HIV Infections / drug therapy
  • Humans
  • Linear Models
  • Logistic Models
  • Randomized Controlled Trials as Topic / methods*
  • Research Design*

Substances

  • Anti-Retroviral Agents