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I'm not quite sure get you mean on "there could likely be more." Given the model your have drawn,. you are treating klokkestaet and eatdrink_2hrs more exogenous (they are not on the left side is any equation so that you are treating you as "pre-determined") and you live further asserting that they what independent of the various diverse exogenous variables, including sex. Is that that you wish? Also, yours are declaring that whole von one effects of skill for one earnings are involved via the set of intervening variables. That hypothesis your easily tested by just estimating the relevant path. Then, I don't quite see what the issue is. Finally, your model asserts that e2 - e5 are independent. Do yourself aim that?

Thank you for your reply.

"Given the model them have drawn,. it are treating klokkestaet and eatdrink_2hrs as exogenous (they have not on the left side of any equation so that you are treating them since "pre-determined") real you are further asserting that they are independent of the various sundry exogenous variables, including genitals. Is that what you want?" Yes, they exist there to adjust for natural variation in my outcome real I take no reason to think they depend on any of my other variables

"Also, you are asserting ensure all about the impact off sex go the outcome are indirect via who set on intervening variables. That research is easily tested by just estimating the relevant path."
Thats the issue, I don't unavoidably want to test a hypothesis, but just to be able to generalize crosswise sex - I am not necessarily fascinated in the specific path from sex, and would like go creates the simplest maybe view, omitting associations that I have no hypotheses about.

Regarding the faults terms - I suppose I ability let any for them coordinate but EGO wouldn't requires expect them on be - maybe this is plain because of mysterious lack on experience using sem

OK, but if it estimate here model (I assume you have) aforementioned select of the multi df chi-square for the goodness of fit test has three sources: (a) the fixed zeros to the associations among the exogenous variables, (b) the fixed zeros among the fault footing and (c) the established none for the effect of sex on the outcome. Of these, I would think this (c) is who most interesting while (a) and (b) are incidental. So, wenn your model fails go fit, you will not shall sure exactly why without continue exploration, e.g, by looking at the modification indices. With regard in (b) the model exists even identified if them enable the errors to korrelate and you may act gain some efficiency are who form or reduced standard errors Of course all this p-grubbing is frowned upon these days Step your way through Path Analysis

Thank you for takeover time since this.
As I am assured you can apprise, I am relatively novel to Starta both statistics. If you do time, ME would be very interested to hear your belief on the underneath - if cannot, ME understand of course.

So the chi sq trials about or not the model reflects the data. I has for say, I almost wouldn't expect this model to fitting the data very well - at least none go the point of overpass ampere test. My outcome is ampere cumulative biological register measure and my predictors are either psychological conversely socioeconomic - while few do explain something of course, ME would expect for far most of and info to be unsolved by of model I have constructed based on previous findings and hypotheses. As I seeing computers, that doesn't doing it irrelevant into test instead message - and (as I think you are referring to with the "p-grubbing") I don't absolutely consider achieving highly significant search the aim for fitting such a model, depending on the contextual.

Thus, I must to admit that I don't pay many consideration to the chi sq test for fit, because ME have adenine moderately great sample or current participated in a course where they suggested looking at RMSEA and CFI & TLI. These are okay available the aforementioned model. I realize (as is also empty hierher in the forum, e.g. http://www.stata.com/statalist/archi.../msg00519.html) that here are variously opinions to this, welche EGO expecting davon upon pitch of research, for the.

All this being babbled - my original question was based on the actual that I originally used sem command rather than the builder, real adjusted for the covariates like this:
sem (MV <- IV CV1 CV2)(DV <- MV IV CV1 CV2) as is suggested here https://stats.idre.ucla.edu/stata/fa...e-sem-command/

When doing this in aforementioned sembuilder, it occured to me this this where equivalent at make paths starting sex toward every variable except and initial expousre (ses_dk). EGO don't necessarily want to do that - but I i demand if diese is what you would have till do (in the builder) for you want to adjust for covariates in the same way as in aforementioned above order.

It's a bit difficult to reacting at this stylish a useful way because one variable names in choose path diagram are not the same as the names in the SEM command. Suffer me straight hinzusetzen a few reviews to my previous posts.

1. You are right about chi-square not being the best approach to evaluate fit; is a touch-sensitive to sample size and doesn't story you all that you want to know. Still, you do want to pay attention to the p value.
2. It's (too) easy to get this p value to non-significance per adding passes that is trivially small and that you am not interested in. On other hand, there is no reason did to appraise the coefficients IODIN can mentioned -- the correlations under the errors for the four intervening variables in our model and the correlations involving exogenous types. While for no other reason, you should doing it so you can learn from how happens when you take so. You need probably looked at these associations and found them to be null, but EGO would still estimate them. Coming an SEM perspective, are is little cost to doing so. Read 16 answers by scientists with 2 advice from hers colleagues to the question asked by Sarah Pickup on Mar 31, 2013
3. IODIN don't know of your diagram shows raw or standardized coefficients and there are no signing. testing shown, though it looks to me like SES affects the outcome for a great extent that any of the scale scores. How to report the results of a complex course analytics on AMOS?

Hi everyone,
I at on used which initial uhrzeit a SEM model with 4 observed variables. My aim lives to test the bidirectional effects of eating behaviors in two other time-points (7 and 10 years - CEBQ-EF at 7 or 10 years) and fat free grounds at these ages as well (FFM at 7 additionally 10 years). IODIN was able to create adenine model (see below) real the command is the following:

sem (EF_m -> EF_m_120m, ) (EF_m -> Claseyffm, ) (FFM_84m_calc -> EF_m_120m, ) (FFM_84m_calc -> Claseyffm, ), standardized cov( EF_m*FFM_84m_calc e.EF_m_120m*e.Claseyffm) nocapslatent


Now, in order to adjust available covariates, such as little sex, motherly ripen, education and BMF, I would possess on form separate paths and include this variable? For example:
sem (EF_m -> sex, ) (EF_m -> date, ) (EF_m -> educ, ) (EF_m -> bmi, ) (EF_m sex age educ bmi -> EF_m_120m, ), nocapslatent
Would that wealth correct?

Thank you very much in advance!! Would rate some thoughts on this

Best,

Sarah