Multi-stage (Cluster) Sampling

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Multi-stage (cluster) sampling is a common sampling design in which the unit of randomization differs from the unit of observation. In other words, the unit at which the treatment is assigned (i.e. community, school) is different than the unit at which surveys are administered (i.e. household, student). This page explains multi-stage (cluster) sampling and provides a demonstration of how to implement it in Stata.

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Overview

Many studies collect data at a different level of observation than the randomization unit. Consider, for example, a researcher who wants to measure the household-level effects of a village-level water sanitation program, or a researcher who wants to measure the student-level effects of a school-level food program. This research design, in which units are assigned to treatments in clusters, is called clustering.

Considerations

How Many Clusters?

To test a program impact convincingly and to precisely estimate treatment effects, it is important to use a sufficient number of clusters. With a small number of clusters, the treatment and control clusters are likely not identical; however, as the number of clusters increases, the more similar and balanced the treatment and control clusters become and the, accordingly, the treatment effect estimate becomes more precise. Typically, clustered sampling designs should include at least 40-50 clusters in each treatment and control group in order to obtain sufficient power and balance at baseline [1]. The exact number of clusters depends on the intra-cluster correlation, sampling and power calculations and the budget, as more clusters is generally more costly.

Standard Errors

In multi-stage (cluster) sampling, since the treatment is assigned to clusters, there are fewer randomized groups than the number of units in the data. Therefore, at the data analysis stage, standard errors for clustered designs must be clustered at the level at which the treatment was assigned.

Implementation

Multi-stage (cluster) sampling must typically be implemented manually. It relies on subsetting the data intelligently to the desired assignment levels. A demonstration follows:

// Use [randtreat] in randomization program
cap prog drop my_randomization
	prog def  my_randomization
	
	// Syntax with open options for [ritest]
	syntax, [*]
	cap drop treatment
	cap drop cluster
	
	//Create cluster indicator
	egen cluster = group(sex agegrp) , label
	  label var cluster "Cluster Group"
	  
	// Keep only one from each cluster for randomization
	preserve
	egen ctag = tag(cluster)
		keep if ctag == 1
		drop ctag
		
		// Group 1/2 in control and treatment
		randtreat, 				///
		  generate(treatment)   /// New variable name
		  multiple(2)			/// Two arms
		
	// Apply assignment to entire cluster
	tempfile ctreat
		save `ctreat' , replace
		restore
	merge m:1 cluster using `ctreat' , nogen
	
	// Cleanup
	lab var treatment "Treatment Arm"
	lab def treatment ///
	  0 "Control"	     ///
	  1 "Treatment"   ///
	  , replace
	lab val treatment treatment
end // 

// Reproducible setup: data, isid, version, seed
sysuse bpwide.dta , clear
	isid patient , sort
	version 13.1
	set seed 796683 // Timestamp: 2019-02-26 22:14:17 UTC
	
// Randomize
my_randomization
ta cluster treatment

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This article is part of the topic Sampling & Power Calculations

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