Funding for this research was provided by:
National Heart, Lung, and Blood Institute (1U01HL143475-01, 5K23HL116427-04)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (5T32HD060550-09)
National Institute of Mental Health (5R25MH08091607)
Received: 5 October 2018
Accepted: 6 May 2019
First Online: 15 May 2019
Ethics approval and consent to participate
: Research activities described in Specific Aim 1 have been approved by the Children’s Hospital of Philadelphia Institutional Review Board (Federal Wide Assurance # 0000459) with a waiver of consent/parental permission per 45 CFR 46.116(d), a waiver of assent per 45 CFR 46.408(a), and a waiver of HIPAA authorization per 45 CFR 164.512(i)(2)(ii) for recruitment purposes and for main study procedures. Research activities described in Specific Aims 2 and 3 are currently under review at the Children’s Hospital of Philadelphia Institutional Review Board (Federal Wide Assurance # 0000459). We will obtain informed consent from all participants. We have requested a waiver of informed consent documentation under 45CFR46.117(c)(1)(ii) because most sessions will take place by telephone.
: Not applicable
: Dr. Landrigan has been supported in part by the Children’s Hospital Association for his work as an Executive Council member of the Pediatric Research in Inpatient Settings (PRIS) network. Dr. Landrigan has consulted with and holds equity in the I-PASS Institute, which seeks to train institutions in best handoff practices and aid in their implementation. In addition, Dr. Landrigan has received monetary awards, honoraria, and travel reimbursement from multiple academic and professional organizations for teaching and consulting on sleep deprivation, physician performance, handoffs, and safety, and has served as an expert witness in cases regarding patient safety and sleep deprivation. The other authors declare that they have no competing interests.
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