Jonas, Daniel E.
Barclay, Colleen http://orcid.org/0000-0002-6093-9576
Grammer, Debbie
Weathington, Chris
Birken, Sarah A.
DeWalt, Darren A.
Shoenbill, Kimberly A.
Boynton, Marcella H.
Mackey, Monique
Riley, Sean
Cykert, Samuel
Funding for this research was provided by:
Agency for Healthcare Research and Quality (1R18HS027078-01)
Article History
Received: 26 March 2021
Accepted: 17 September 2021
First Online: 16 November 2021
Declarations
:
: All procedures performed in studies involving human participants were in accordance with the ethical standards of the University of North Carolina Institutional Review Board (UNC IRB) and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Informed consent was obtained electronically from all individual participants included in the study (i.e., the practice providers and staff who completed study surveys), via emails sent by study staff. The institutional review board approved a full waiver of informed consent for patients because patients at participating practices receive recommended routine care, and no individual-level patient data is collected by the study team. Important modifications to the protocol are submitted to the UNC IRB and to ExternalRef removed.
: Not applicable
: The authors declare that they have no competing interests.