Funding for this research was provided by:
National Institute on Aging (R01 AG030618-05A1, R01 AG040220-05, R01AG045157, R01AG055391, AG045157, P30AG10133, 5R01AG045350, R01AG054205-02, 2P30AG010133, K23-AG043476)
National Heart, Lung, and Blood Institute (R01 HL128494, R01HL131730, 5T32HL091816-07)
Centers for Medicare and Medicaid Services (1 L1 CMS331444-02-00)
National Center for Advancing Translational Sciences (UL1TR001108, UL1TR001108 (Project Development Team))
Agency for Healthcare Research and Quality (P30 HS024384-02)
U.S. Department of Defense (AZ160032)
Text and Data Mining valid from 2018-03-27
Received: 5 October 2017
Accepted: 28 February 2018
First Online: 27 March 2018
Ethics approval and consent to participate
: The protocol was approved by the Institutional Review Board at the Indiana University School of Medicine, #1608126693. The principal investigator and the research staff are responsible for conducting the informed consent process with all the study participants. Informed consent will be obtained from the subject or their legally authorized representative as appropriate. Changes to the study protocol and/or the informed consent will be sent to the Institutional Review Board as protocol amendments. All data will be de-identified prior to analysis; only the principal investigator and project manager will be able to access the code to identify the individual. The protocol was registered in ClinicalTrials.gov NCT03095417 on March 23, 2017 (ExternalRef removed) before starting the trial, and trial status will be updated accordingly.
: Not applicable.
: The authors declare that they have no competing interests. The funding agency had no role in the development of the study design, collection, analysis, interpretation of data, manuscript development, or the decision to submit the manuscript for publication.
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