Funding for this research was provided by:
National Institute of Mental Health (R01 MH074394, R01 MH074399)
Text and Data Mining valid from 2019-04-26
Received: 31 July 2017
Accepted: 21 March 2019
First Online: 26 April 2019
Ethics approval and consent to participate
: This study was approved by Yale University (26962), and Clinical Directors Network (004–06), Bronx Lebanon Hospital Center (05 08 08 02), Biomedical Research Alliance of New York (08–02-242(HHC)-202), Brookdale University Hospital and Medical Center (07–18), Brooklyn Hospital Center (624), Columbia University Medical Center (IRB-AAAD1707), Flushing Hospital (08/07–1), Lutheran Medical Center (53), and Public Health Solutions (032607). All participants provided written informed consent. The IRBs for 12 of the 14 study sites waived the parental informed consent requirement for participants aged 14–17, because the study was low risk and participants were independently consenting to their own prenatal care per New York State law. Thus, these IRBs considered these participants mature minors, able to independently provide informed consent for this study. Two of the 14 study sites’ local IRBs required parental consent. For those participants, both parental informed consent and minor assent was obtained.
: Not applicable.
: The authors declare that they have no competing interests.
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