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From |
anna bargagliotti <[email protected]> |

To |
[email protected] |

Subject |
Re: st: Re: psmatch2 question |

Date |
Wed, 25 Aug 2010 12:53:33 -0700 (PDT) |

Thanks Austin and Steve! Let me restate in my own words to see if I understand.. My goal is to compare the gpas of treatments vs a matched control. The psmatch2 command computed propensity score for each student. In order to produce a more accurate t-stat than the ATT t-stat given by the psmatch2 command, I can regress gpa on the treatment dummy and a set of X variables using the pscore as a pweight. I do this for the whole sample (ie, those students that were treated, those that were matched, and those that were unmatched). This will produce a t-stat on the treatment dummy which will in turn give me the wanted comparison. Thank you very much for your help! This has been great! ----- Original Message ---- From: Austin Nichols <[email protected]> To: [email protected] Sent: Wed, August 25, 2010 9:07:22 AM Subject: Re: st: Re: psmatch2 question Steve, Anna, et al.-- The bootstrap is not a priori a good idea: http://www.nber.org/papers/t0325 But if you use nonparametric propensity scores, or equivalently a logit with only mutually exclusive exhaustive dummies as explanatory variables, and reweight instead of matching 1:1 or somesuch, you will be better off in many ways; see e.g. Hirano, K., G. Imbens, and G. Ridder. (2003). “Efficient Estimation of Average Treatment Effects Using the Estimated Propensity Score,” Econometrica, 71(4): 1161-1189. The t-stat produced by -psmatch2- is not particularly reliable, compared to one produced by a double-robust regression, say, where you regress the outcome on treatment and other explanatory variables using weights based on propensity scores. But the t-stat on the ATT is intended to guide you to reject or fail to reject the hypothesis that the effect of treatment on those who received treatment is zero. If you decide to bootstrap, save each estimated ATT and its SE and see how the matching estimator's SE compares to the observed standard deviation of estimates; then do the same with the nonparametric propensity score reweighting estimator and you will probably decide not to match but to reweight. A minor point: estimated propensity scores are never "more accurate" than the unknown true scores, but even if you knew the true propensity scores, you could get more efficient estimates in many cases by throwing that information away and estimating propensity scores. This is why computing a SE as if the propensity scores are fixed and known is reasonable. Instead of the presentation, you may want the papers: http://www.stata-journal.com/article.html?article=st0136 http://www.stata-journal.com/article.html?article=st0136_1 http://www-personal.umich.edu/~nicholsa/ciwod.pdf http://www-personal.umich.edu/~nicholsa/erratum.pdf On Wed, Aug 25, 2010 at 5:51 AM, Steve Samuels <[email protected]> wrote: > -- > > Anna, > > First, I must apologize. I showed a method for estimating the ATT > (weighting by propensity scores) which is different from the one that > -psmatch2- uses (matching on propensity scores). So my program does > not apply to your analysis. The -help- for -psmatch2- illustrates a > bootstrap approach to estimating the standard error, although it > states that it is "unclear whether the bootstrap is valid in this > context." > > Also, there is literature (see page 26 of Austin Nichols's presentation > http://repec.org/dcon09/dc09_nichols.pdf) which suggests that > estimated propensity scores might be more accurate than the unknown > true scores; if so, then standard errors which consider the estimated > scores as known might be better than the bootstrapped standard errors! > So there is apparently no right answer. I think that a conservative > approach would be to use the -bootstrap- technique shown in the > -psmatch2- help, followed by "estat bootstrap, all" to get confidence > intervals for ATT. > > ATT is one of several methods for describing the causal effect of a > treatment: To quote Austin's presentation (p 15): "For evaluating the > eﬀect of a treatment/intervention/program, we may want to estimate the > ATE for participants (the average treatment eﬀect on the treated, or > ATT) or for potential participants who are currently not treated (the > average treatment eﬀect on controls, or ATC), or the ATE across the > whole population (or even for just the sample under study)." > > Best wishes > > Steve > > On Tue, Aug 24, 2010 at 7:23 PM, anna bargagliotti <[email protected]> wrote: >> Thank you for your insights about bootstrapping. I wiill try adjusting your >> code to my situation to reproduce the T-stat and compute the p-value. >> >> I am, however, still confused about two very simple things: >> 1. What is the T-stat for the ATT actually telling us? Is this the T-stat >for >> the comparison of treatment vs control matched groups? >> 2. How do we determine if there is a treatment effect? * * For searches and help try: * http://www.stata.com/help.cgi?search * http://www.stata.com/support/statalist/faq * http://www.ats.ucla.edu/stat/stata/ * * For searches and help try: * http://www.stata.com/help.cgi?search * http://www.stata.com/support/statalist/faq * http://www.ats.ucla.edu/stat/stata/

**Follow-Ups**:**Re: st: Re: psmatch2 question***From:*Austin Nichols <[email protected]>

**References**:**st: Anyone has the Stata code for National Nursing Home Survey of various years***From:*"G. Dai" <[email protected]>

**st: RE: Anyone has the Stata code for National Nursing Home Survey of various years***From:*Nick Cox <[email protected]>

**st: psmatch2 question***From:*anna bargagliotti <[email protected]>

**st: Re: psmatch2 question***From:*"Joseph Coveney" <[email protected]>

**Re: st: Re: psmatch2 question***From:*Steve Samuels <[email protected]>

**Re: st: Re: psmatch2 question***From:*anna bargagliotti <[email protected]>

**Re: st: Re: psmatch2 question***From:*Steve Samuels <[email protected]>

**Re: st: Re: psmatch2 question***From:*Austin Nichols <[email protected]>

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