{smcl}
{* *! version 0.9.1 Aug 2017}{...}
{title:Title}

{pstd}
{hi:rddsga} {hline 2} Subgroup analysis for regression discontinuity designs using inverse propensity score weighting


{title:Syntax}

{p 8 16 2}
{cmd:rddsga} {depvar} {it:assignvar} [{indepvars}] {ifin}
{cmd:,} {it:options}
{p_end}

{phang}
{it:depvar} is the outcome variable, {it:assignvar} is the assignment variable for which there is a known cutoff and {it:indepvars} are a set of control variables.
{p_end}

{synoptset 22 tabbed}{...}
{synopthdr}
{synoptline}
{syntab :Subgroup and RDD}
{p2coldent:* {opth sg:roup(varname)}}subgroup indicator variable{p_end}
{synopt :{opth t:reatment(varname)}}indicator for actual treatment status; if not specified, a sharp RDD is assumed{p_end}
{synopt :{opt c:utoff(real)}}specifies the cutoff value in {it:assignvar}; default is 0{p_end}
{p2coldent:* {opt bw:idth(real)}}specifies the bandwidth around the cutoff{p_end}

{syntab :Balance}
{p2coldent:+ {opth bal:ance(varlist)}}variables that enter the propensity score estimation; default is {indepvars}{p_end}
{synopt :{opt probit}}predict propensity score using a {manhelp probit R:probit} model; default is {manhelp logit R:logit}{p_end}
{synopt :{opt nocom:sup}}do not restrict sample to area of common propensity score support{p_end}

{syntab :Model}
{synopt :{opt first:stage}}estimate the discontinuity in the treatment probability using OLS{p_end}
{synopt :{opt reduced:form}}estimate the reduced form effect using OLS{p_end}
{synopt :{opt iv:regress}}estimate the treatment effect using instrumental variable regression; requires that a treatment variable is specified in {opt treatment(varname)}{p_end}
{synopt :{opt quad:ratic}}use quadratic spline; default is linear{p_end}
{synopt :{opth vce(vcetype)}}{it:vcetype} may be {opt un:adjusted},
   {opt r:obust}, {opt cl:uster} {it:clustvar}, {opt boot:strap},
   {opt jack:knife}, or {opt hac} {help ivregress##kernel:{it:kernel}}; default is {opt bootstrap}{p_end}
{synopt :{opt noboot:strap}}do not compute bootstrap standard errors for RD estimates{p_end}
{synopt :{opt r:eps(#)}}perform # bootstrap replications; default is {opt reps(50)}{p_end}
{synopt :{opt noipsw}}do not use inverse propensity score weighting{p_end}

{syntab :Reporting and Output}
{synopt :{opt dibal:ance}}display original balance and propensity score-weighted balance tables and statistics{p_end}
{synopt :{opth ipsw:eight(newvar)}}name of new variable for the inverse propensity score weight for each observation; if not specified, no variable will be generated{p_end}
{synopt :{opth com:sup(newvar)}}name of new binary variable indicating common support; if not specified, no variable will be generated{p_end}
{synopt :{opth psc:ore(newvar)}}name of new variable for the estimated propensity score; if not specified, no variable will be generated{p_end}
{synoptline}
{p2colreset}{...}
{p 4 6 2}* These options must be specified.{p_end}
{p 4 6 2}+ This option must be specified if {it:indepvars} is empty.{p_end}
{p 4 6 2}{it:indepvars} may contain factor variables; see {help fvvarlist}.{p_end}


{marker description}{...}
{title:Description}

{pstd}
{cmd:rddsga} allows to conduct a binary subgroup analysis in RDD settings based on inverse propensity score weights (IPSW).
Observations in each subgroup are weighted by the inverse of their conditional probabilities to belong to that subgroup, given a set of covariates.
Analyzing the differential treatment effect in the reweighted sample helps isolating the difference due to the subgroup characteristic of interest from other observable dimensions.

{pstd}
{cmd:rddsga} computes IPSW based on the vector of covariates in {it:indepvars}, which are also used as control variables in the model.
A separate set of variables to compute IPSW may be optionally specified with {opt balance(varlist)}.
A new variable with IPSW may be generated using {opt psweight(newvar)}.
In order to assess the statistical significance of the difference in means for each covariate, {cmd:rddsga} uses a t-test on the equality of means and reports the resulting p-value, as well as the (weighted) standardized mean difference.
Joint significance is assessed using an F-test.
The resulting balance tables are stored as matrices (see {help rddsga##results:stored results} below), and may also be displayed using {opt dibalance}.

{pstd}
Options {opt firststage}, {opt reducedform} and {opt ivregress} may be used to estimate the first stage, reduced form and treatment effects using OLS and IV methods, respectively.
Standard variance estimator options may be used for these estimators with {opt vce(vcetype)}.
The estimated coefficients for the interaction of indicator variables for each subgroup and a treatment indicator are reported, along with bootstrap standard errors (unless other {it:vcetype} is specified).

{pstd}
Additional details regarding the methodology implemented by {cmd: rddsga} can be found in the project's {browse "https://gitlab.com/acarril/rddsga/wikis/home":repository}.
An application can be found in {help rddsga##mainpaper:Gerardino, Litschig, Olken and Pomeranz (2017)}.


{marker options}{...}
{title:Options}

{dlgtab:RD design}

{phang}
{opt sgroup(varname)} specifies a subgroup indicator variable.
This variable must be a {it:dummy} (values 0 or 1).
This option must be specified.

{phang}
{opt treatment(varname)} specifies an indicator variable for actual treatment status.
If not specified, a sharp RDD is assumed.

{phang}
{opt cutoff(real)} specifies the cutoff value in {it:assignvar}; default is 0 (assuming normalized {it:assignvar}).

{phang}
{opt bwidth(real)} specifies a symmetrical the bandwidth around the cutoff.
This option must be specified.

{dlgtab:Balance}

{phang}
{opt balance(varlist)} specifies the variables that enter the propensity score estimation.
If not specified, variables in {it:indepvars} are used.
This option is useful if one wants to balance a different set of covariates than the ones used as controls in the model.
This option must be specified if {it:indepvars} is empty.

{phang}
{opt probit} indicates that the propensity score is computed after a fitting a  {manhelp probit R:probit} model; default is {manhelp logit R:logit}.

{phang}
{opt nocomsup} indicates that the sample is not to be restricted to the area of common support.

{marker options_model}{...}
{dlgtab:Model}

{phang}
{opt firststage} estimates the discontinuity in the treatment probability using OLS.

{phang}
{opt reducedform} estimates the reduced form effect using OLS.

{phang}
{opt ivregress} estimates the treatment effect using instrumental variable regression.
If specified, it requires that a treatment variable is also specified in {opt treatment(varname)}.
See {help ivregress} for additional information.

{phang}
{opt quadratic} indicates that a quadratic spline is to be used for full interaction with subgroup indicators. If not specified, a linear spline is used.

{phang}
{opt vce(vcetype)} specifies the variance estimators options.
{it:vcetype} may be unadjusted, robust, cluster clustvar, bootstrap, jackknife, or hac kernel (see {help  vce_option}).
Bootstrap is used by default, unless {opt nobootstrap} is used (see below), or a different {it:vcetype} is specified.

{phang}
{opt nobootstrap} prevents computing bootstrap standard errors, which is the default.

{phang}
{opt reps(#)} perform # bootstrap replications; default is {opt reps(50)}.

{phang}
{opt noipsw} prevents employing inverse propensity score weighting for the estimations.

{marker options_reporting}{...}
{dlgtab:Reporting}

{phang}
{opt dibalance} display original balance and propensity score weighting balance tables and statistics.
This balance is computed for each covariate in {it:indepvars}, unless {opt balance(varlist)} is specified.

{phang}
{opt psweight(newvar)} specifies a name for a new variable with the propensity score weighting. If not specified, no variable will be generated.

{phang}
{opt comsup(newvar)} specifies a name for a new binary variable indicating common support. If not specified, no variable will be generated.

{phang}
{opt pscore(newvar)} specifies a name for a new variable with the propensity score. If not specified, no variable will be generated.


{marker examples}{...}
{title:Examples}

{pstd}Setup (click {browse "https://github.com/acarril/rddsga#installation":here} for details on getting ancillary files){p_end}
{phang2}{cmd:. use rddsga_synth}{p_end}

{pstd}Assess covariate imbalance using one covariate{p_end}
{phang2}{cmd:. rddsga Y Z, balance(X1) sgroup(G) bwidth(10) dibal}{p_end}

{pstd}Silently store computed IPSW based on X1 and X2{p_end}
{phang2}{cmd:. rddsga Y Z, balance(X1 X2) sgroup(G) bwidth(10) ipsweight(ipsw)}{p_end}

{pstd}Fit reduced form model{p_end}
{phang2}{cmd:. rddsga Y Z, balance(X1 X2) sgroup(G) bwidth(10) reduced}{p_end}

{pstd}Estimate treatment effect in fuzzy RDD using instrumental variables regression and 200 bootstrap replications, comparing output without and with IPSW{p_end}
{phang2}{cmd:. rddsga Y Z X1 X2, sgroup(G) bwidth(6) ivreg bsreps(100) treatment(T) noipsw}{p_end}
{phang2}{cmd:. rddsga Y Z X1 X2, sgroup(G) bwidth(6) ivreg bsreps(100) treatment(T)}{p_end}


{marker results}{...}
{title:Stored results}

{pstd}
{cmd:rddsga} stores the following in {cmd:e()}:

{synoptset 20 tabbed}{...}
{p2col 5 20 24 2: Scalars}{p_end}
{synopt:{cmd:e(ipsw_N_G0)}}number of observations in subgroup 0 (IPSW){p_end}
{synopt:{cmd:e(ipsw_N_G1)}}number of observations in subgroup 1 (IPSW){p_end}
{synopt:{cmd:e(ipsw_Fstat)}}F-statistic (IPSW){p_end}
{synopt:{cmd:e(ipsw_pvalue)}}F-statistic p-value (IPSW){p_end}
{synopt:{cmd:e(ipsw_avgdiff)}}Average of absolute values of standardized differences (IPSW){p_end}

{synopt:{cmd:e(unw_N_G0)}}number of observations in subgroup 0 (unweighted){p_end}
{synopt:{cmd:e(unw_N_G1)}}number of observations in subgroup 1 (unweighted){p_end}
{synopt:{cmd:e(unw_Fstat)}}F-statistic (unweighted){p_end}
{synopt:{cmd:e(unw_pvalue)}}F-statistic p-value (unweighted){p_end}
{synopt:{cmd:e(unw_avgdiff)}}Average of absolute values of standardized differences (unweighted){p_end}

{p2col 5 15 19 2: Matrices}{p_end}
{synopt:{cmd:e(b)}}subgroup estimators coefficient vector{p_end}
{synopt:{cmd:e(V)}}variance-covariance matrix of the estimators{p_end}

{synopt:{cmd:e(ipsw)}}balance table matrix (IPSW){p_end}
{synopt:{cmd:e(unw)}}balance table matrix (unweighted){p_end}
{p2colreset}{...}

{pstd}
Additionally, {cmd:rddsga} stores all macros and scalars of the estimated model ({opt firststage}, {opt firststage} or {opt ivregress}; see {help rddsga##options_model:Model options} above).
Refer to the {help regress##results:Stored Results} section of {manhelp regress R:regress} for the full list of macros and scalars additionally stored in {cmd:e()}.


{marker authors}{...}
{title:Authors}

{pstd}
Alvaro Carril (maintainer){break}
J-PAL LAC{break}
acarril@fen.uchile.cl

{pstd}
Andre Cazor{break}
J-PAL LAC{break}

{pstd}
Maria Paula Gerardino{break}
Inter-American Development Bank{break}

{pstd}
Stephan Litschig{break}
National Graduate Institute for Policy Studies{break}

{pstd}
Dina Pomeranz{break}
University of Zurich{break}


{marker disclaimer}{...}
{title:Disclaimer}

{pstd}
This software is provided "as is", without warranty of any kind.
If you have suggestions or want to report problems, please create a new issue in the {browse "https://github.com/acarril/rddsga/issues":project repository} or contact the project maintainer.
All remaining errors are our own.


{marker references}{...}
{title:References}

{marker mainpaper}{...}
{phang}Gerardino, Maria Paula, Stephan Litschig, Benjamin Olken, and Dina Pomeranz. 2017.
"Can Audits Backfire? Evidence from Public Procurement in Chile".
{it:Working Paper}.