Hello everyone,
I am trying to find the impact of myoinositol on triceps skin fold thickness in newborns using linear regression analysis. I used graph as well as statistical approaches to investigate the homoscedasticity of the model itself - residual vs fitted plot and Breusch - Pagan / cook - weinberg test for heteroskedasticity. The residual vs fitted plot of my model , personally, I think it looks fine even though some residuals kind of slightly diverting from the middle line as the fitted values increase. Yet, in general, those dots seem to equally distribute along the line.
But the p value I obtained from Breusch- Pagen by typing estat hettest for this particular model is less than 0.001. Does it raise any concerns? And is the "robust" the only way to fix this?
Or should I construct my model again in order to meet the assumption of homoscedasticity?

Thank you for your comments and suggestaions in advance.
BW
Em
I am trying to find the impact of myoinositol on triceps skin fold thickness in newborns using linear regression analysis. I used graph as well as statistical approaches to investigate the homoscedasticity of the model itself - residual vs fitted plot and Breusch - Pagan / cook - weinberg test for heteroskedasticity. The residual vs fitted plot of my model , personally, I think it looks fine even though some residuals kind of slightly diverting from the middle line as the fitted values increase. Yet, in general, those dots seem to equally distribute along the line.
But the p value I obtained from Breusch- Pagen by typing estat hettest for this particular model is less than 0.001. Does it raise any concerns? And is the "robust" the only way to fix this?
Or should I construct my model again in order to meet the assumption of homoscedasticity?
Thank you for your comments and suggestaions in advance.

BW
Em
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