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Authors
Kurth, Lisa
O’Shea, T. Michael
Burd, Irina
Dunlop, Anne L.
Croen, Lisa
Wilkening, Greta
Hsu, Ting-ju
Ehrhardt, Stephan
Palanisamy, Arvind
McGrath, Monica
Churchill, Marie L.
Weinberger, Daniel
Grados, Marco
Dabelea, Dana
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Funding
Funding for this research was provided by:
NIH Office of the Director (U2COD023375, U24OD023382, U24OD023319, UH3OD023248, UH3OD023318, UH3OD023348, UH3OD023320, UH3OD023253, UH3OD023313, UH3OD023279, UH3OD023289, UH3OD023282, UH3OD023365, UH3OD023244, UH3OD023275, UH3OD023271, UH3OD023347, UH3OD023389, UH3OD023268, UH3OD023342, UH3OD023349, UH3OD023285, UH3OD023290, UH3OD023272, UH3OD023249, UH3OD023337, UH3OD023305)
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Article History
Received: 7 February 2023
Accepted: 27 April 2024
First Online: 26 May 2024
Declarations
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: 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. ECHO Cohort Investigators (or their designated study personnel) obtain written informed consent or parent’s / guardian’s permission along with child assent as appropriate, for ECHO-wide Cohort Data Collection Protocol participation and for participation in their specific cohorts. The work of the ECHO Data Analysis Center is approved through the Johns Hopkins Bloomberg School of Public Health Institutional Review Board.
: Not applicable.
: The authors have no conflicts of interest relevant to this article to disclose.
