Meier, Emily R.
Creary, Susan E.
Heeney, Matthew M.
Dong, Min
Appiah-Kubi, Abena O.
Nelson, Stephen C.
Niss, Omar
Piccone, Connie
Quarmyne, Maa-Ohui
Quinn, Charles T.
Saving, Kay L.
Scott, John P.
Talati, Ravi
Latham, Teresa S.
Pfeiffer, Amanda
Shook, Lisa M.
Vinks, Alexander A.
Lane, Adam
McGann, Patrick T. https://orcid.org/0000-0001-6198-4785
Funding for this research was provided by:
Doris Duke Charitable Foundation (2017090)
Article History
Received: 17 June 2020
Accepted: 17 November 2020
First Online: 27 November 2020
Ethics approval and consent to participate
: The study protocol is approved by the Institutional Review Board of each participating institution prior to the enrollment of participants. Written, informed consent to participate is or will be obtained from participants (or their legal guardian in the case of children under age 18 years). Assent will also be obtained for children< 18 years of age per each local IRB. All protocol modifications are relayed to relevant parties, including all IRBs, ClinicalTrials.gov, and participants as needed.
: Consent for publication is not applicable, as the manuscript does not contain any individual data.
: The authors declare that they have no competing interests.