Document is current
Any future updates will be listed below
-
Authors
Shuffrey, Lauren C. http://orcid.org/0000-0003-3631-5971
Lucchini, Maristella
Morales, Santiago
Sania, Ayesha
Hockett, Christine
Barrett, Emily
Carroll, Kecia N.
Cioffi, Camille C.
Dabelea, Dana
Deoni, Sean
Dunlop, Anne L.
Deutsch, Arielle
Fifer, William P.
Firestein, Morgan R.
Hedderson, Monique M.
Jacobson, Melanie
Kelly, Rachel S.
Kerver, Jean M.
Mason, W. Alex
Mirzakhani, Hooman
O’Connor, Thomas G.
Trasande, Leonardo
Weiss, Scott
Wright, Rosalind
Zhu, Yeyi
Crum, Rosa M.
Lee, Seonjoo
Elliott, Amy J.
Monk, Catherine
,
-
Funding
Funding for this research was provided by:
NIH Office of the Director (U2COD023375, U24OD023382, U24OD023319, UH3 OD023248, UH3 OD023313, UH3 OD023328, UH3 OD023318, UH3 OD023279, UH3 OD023349, UH3 OD023285, UH3 OD023271, UH3 OD023305, UH3 OD023337, UH3 OD023289, UH3 OD023389)
National Institute of Child Health and Human Development (K99HD103910)
Office of Research on Women's Health (UH3 OD023279-05S1)
- License Information
-
More Information
Article History
Received: 27 May 2022
Accepted: 14 September 2022
First Online: 8 October 2022
Declarations
:
: The ECHO-wide protocol is under a single IRB—which is of Western Institutional Review Board (WIRB) Copernicus Group IRB. WCG IRB is registered with the Office for Human Research Protections (OHRP and FDA) as IRB00000533. Properly constituted Institutional Review Boards – either the ECHO single IRB or the ECHO cohort's local IRB – are accountable for compliance with regulatory requirements for the ECHO-wide Cohort Data Collection Protocol at participating cohort sites. Governing IRBs review ECHO protocols and all informed consent/assent forms, HIPAA authorization forms, recruitment materials, and other relevant information prior to the initiation of any ECHO-wide Cohort Data Collection Protocol-related procedures or activities. The work of the ECHO Data Analysis Center is approved through the Johns Hopkins Bloomberg School of Public Health Institutional Review Board. ECHO Cohort Investigators (or their designated study personnel) obtained written informed consent from all participants in the current study for ECHO-wide Cohort Data Collection Protocol participation and for participation in their specific cohorts.
: Not applicable.
: The authors have no conflicts to declare.
