O’Neil, Meghan M.
Johnson, Rebecca A.
Córdova, David
Pryor, Jenna
Pinals, Debra A.
Funding for this research was provided by:
National Science Foundation (2017068, 2017068, 2017068, 2017068, 2017068)
National Institutes of Health (L32)
Article History
Received: 12 January 2023
Accepted: 20 February 2023
First Online: 6 March 2023
Declarations
:
: The study was approved by the Health Sciences and Behavioral Sciences Institutional Review Board (IRB-HSBS) of the University of Michigan, reference number: HUM00152102. Protocol amendments, if needed, are to be processed through the IRB for approval. All methods will be performed in accordance with the relevant guidelines and regulations outlined by the IRB-HSBS and the Declaration of Helsinki. Written informed consent will be obtained by research staff in person with clients prior to enrollment in the study. Model informed consent forms may be requested from the PI. Participants consent at enrollment to data linkage that awards the research team a maximum of 10 years of access to the data, including the planned two-year annual linkage with administrative data. Personal information will be collected with Qualtrics survey tools during the in-person survey administration. See data management section of the IRB for data security details, available upon request from the PI. A data monitoring committee is not required or recommended under the IRB. Identifying information will only be shared with authorized officials on a need-to-know basis, including for instance, the Unemployment Insurance Agency, for data linkage purposes and will be done utilizing a secure server with Duo two-factor authentication. Eligible participants will only be identified with first name, last initial when scheduling enrollment visits as to maintain anonymity. Adverse events and trial conduct will be reported by PI per IRB-HSBS HUM00152102 guidelines. In accordance with the provisions of Sect. 301(d) of the Public Health Service Act, 42 U.S.C. 241(d), a certificate of confidentiality has been issued by the National Institutes of Health (CC-OD-20-1084). Participants are advised in consent forms that the survey instrument includes sensitive topics. They are advised if they become emotionally distressed while completing the survey, they can request a counseling session with a recovery support specialist.
: N/A.
: National Science Foundation (NSF), 2415 Eisenhower Avenue, Alexandria, Virginia 22314, USA Tel: (703) 292–5111. National Institutes of Health (LRP), 6700B Rockledge Drive, Suite 2300, Bethesda, MD 20892, USA Tel: (866) 849–4047. University of Michigan, 426 Thompson Street, Ann Arbor, MI, 48104, USA Tel: (734) 764–4636.
: N/A.
: All authors declare that they have no competing interests.