Eagle, Shawn R. https://orcid.org/0000-0001-6767-1042
Asken, Breton
Trbovich, Alicia
Houck, Zachary M.
Bauer, Russell M.
Clugston, James R.
Broglio, Steven P.
McAllister, Thomas W.
McCrea, Michael A.
Pasquina, Paul
Collins, Michael W.
Kontos, Anthony P.
,
Putukian, Margot
Hoy, April
Ortega, Justus
Port, Nicholas
Buckley, Thomas
Kaminski, Thomas
Houston, Megan
Duma, Stephen
Miles, Chris
Lintner, Laura
Funding for this research was provided by:
u.s. department of defense (W81XWH1420151)
Article History
Accepted: 21 February 2022
First Online: 14 March 2022
Declarations
:
: This publication was made possible, in part, with support from the Grand Alliance CARE Consortium, funded in part by the NCAA and the DoD. The US Army Medical Research Acquisition Activity, 820 Chandler Street, Fort Detrick, MD 21702–5014, is the awarding and administering acquisition office. This work was supported by the Office of the Assistant Secretary of Defense for Health Affairs, through the Combat Casualty Care Research Program, endorsed by the DoD, through the Joint Program Committee 6/Combat Casualty Care Research Program—Psychological Health and Traumatic Brain Injury Program under Award No. W81XWH1420151.
: Shawn R. Eagle, Breton Asken, Alicia Trbovich, Zachary M. Houck, Russell M. Bauer, James R. Clugston, Steven P. Broglio, Thomas W. McAllister, Michael A. McCrea, Paul Pasquina, Michael W. Collins, Anthony P. Kontos, and the CARE Consortium Investigators declare no competing interests.
: The complete NCAA/DoD database is available on FITBIR.
: Not applicable.
: SE, BA, and AK designed the study, conducted the analyses, and wrote and reviewed the manuscript. AT, ZH, RB, JC, and MC contributed to analytical design, writing, and critical review of the manuscript. SB TM, MM, PP are the primary principal investigators of the NCAA/DoD CARE Consortium study and contributed to the overall study design and critical review of the manuscript. MP, AH, JO, NP, TB, TK, MH, SD, CM, and LL contributed to data collection and critical review of the manuscript.
: This study was approved by each participating site’s IRB for human subjects’ research.
: Participants completed written informed consent prior to initiating study procedures<b>.</b>
: Not applicable.