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Authors
Gesell, Sabina B.
Bushnell, Cheryl D.
Jones, Sara B.
Coleman, Sylvia W.
Levy, Samantha M.
Xenakis, James G.
Lutz, Barbara J.
Bettger, Janet Prvu
Freburger, Janet
Halladay, Jacqueline R.
Johnson, Anna M.
Kucharska-Newton, Anna M.
Mettam, Laurie H.
Pastva, Amy M.
Psioda, Matthew A.
Radman, Meghan D.
Rosamond, Wayne D.
Sissine, Mysha E.
Halls, Joanne
Duncan, Pamela W.
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Funding
Funding for this research was provided by:
National Center for Advancing Translational Sciences (UL1TR001420)
Patient-Centered Outcomes Research Institute (PCS-1403-14532)
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Article History
Received: 17 July 2019
Accepted: 22 November 2019
First Online: 19 December 2019
Ethics approval and consent to participate
: Institutional review board (IRB) approval was received through Wake Forest University Health Sciences (central IRB), or through local hospital IRBs. At 90 days during the telephone survey, patients provided informed, verbal consent [CitationRef removed] for collection of outcomes, the ethics committees agreed with the verbal consent and HIPAA authorization process and approved this procedure. Additionally, participants consented to collection of process measures, including the ORIC and Partnership Synergy Scale via email survey.
: Not applicable.
: Drs. Duncan, Bushnell, and Dr. Bushnell: ownership Interest, Care Directions, the company that integrates the electronic care plan application used in the study (COMPASS-CP) into electronic health records; Others: None.
