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Authors
Quintero, Stephanie M.
Strassle, Paula D.
Londoño Tobón, Amalia
Ponce, Stephanie
Alhomsi, Alia
Maldonado, Ana I.
Ko, Jamie S.
Wilkerson, Miciah J.
Nápoles, Anna María
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Funding
Funding for this research was provided by:
Division of Intramural Research, National Institute on Minority Health and Health Disparities
National Institutes of Health
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Article History
Received: 14 June 2022
Accepted: 15 March 2023
First Online: 17 March 2023
Declarations
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: This analysis utilized de-identified data, therefore did not qualify as human subjects research per federal regulation based on the 2018 revisions to the Common Rule exemptions found in 45 CFR 46.104(d). This study was performed in accordance with the Declaration of Helsinki.The PRAMS protocol was reviewed and approved by the U.S. Centers for Disease Control and Prevention Institutional Review Board (IRB) and the IRBs of the individual health departments participating in the state PRAMS projects. According to the approved protocol, an informed consent document is included within each survey packet explaining the participant’s rights. No written consent is required for surveys returned by mail; consent was implied if the survey is completed and returned. If the interview was completed by telephone, the informed consent document is read verbally on the telephone, and verbal consent is obtained from the participant prior to proceeding with the survey. For more information on informed consent of the PRAMS study please refer to, [ExternalRef removed].
: Not applicable.
: The authors declare no competing interests.
