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Authors
Kerlin, Meeta Prasad https://orcid.org/0000-0002-3239-1443
Small, Dylan
Fuchs, Barry D.
Mikkelsen, Mark E.
Wang, Wei
Tran, Teresa
Scott, Stefania
Belk, Aerielle
Silvestri, Jasmine A.
Klaiman, Tamar
Halpern, Scott D.
Beidas, Rinad S.
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Funding
Funding for this research was provided by:
national heart, lung, and blood institute (R01HL141608)
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Article History
Received: 14 July 2021
Accepted: 25 July 2021
First Online: 10 August 2021
Declarations
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: The University of Pennsylvania institutional review board (IRB) served as the single IRB for four of the five study hospitals, in compliance with the National Institutes for Health. The fifth hospital required a separate protocol within the hospital’s IRB. The study was approved by both the University of Pennsylvania IRB (Protocol # 833400) and the Chester County Hospital IRB (Protocol # CCH19-05) with a waiver of informed consent due to the minimal risk to participants and infeasibility of conducting the pragmatic trial of ICU-level interventions if individual consent were required.
: Not applicable
: Rinad Beidas receives royalties from Oxford University Press. She has served as a consultant to Camden Coalition of Healthcare Providers. She provides consultation to United Behavioral Health. She serves on the Clinical and Scientific Advisory Board for Optum Behavioral Health. Scott Halpern is a paid member of the Steering Committee for the NIA-funded IMPACT Collaboratory and receives consulting fees from Atrium Health and Georgia State University. The rest of the authors declare that they have no competing interests.
