Multicomponent Informed Consent with Marshallese Participants

Author:

Purvis Rachel S.1,Ayers Britni L.1,Bogulski Cari A.1,Kaminicki Kyle F.1,Haggard-Duff Lauren K.1,Riklon Lynda A.1,Iban Anita2,Mejbon-Samuel Rotha3,Lakmis Rumina4,Riklon Sheldon1ORCID,Thompson Joseph W.5,McElfish Pearl A.1ORCID

Affiliation:

1. University of Arkansas for Medical Sciences Northwest, Fayetteville, USA

2. Faith in Action Research and Resource Alliance (FARRA), Springdale, USA

3. Marshallese Educational Initiative (MEI), Springdale, USA

4. Arkansas Children’s Hospital, Bethel Heights, USA

5. University of Arkansas for Medical Sciences, Little Rock, USA

Abstract

Pacific Islanders are the second fastest-growing population in the United States; however, Pacific Islanders, and Marshallese specifically, are underrepresented in health research. A community-based participatory research (CBPR) approach was used to engage Marshallese stakeholders and build an academic-community research collaborative to conduct health disparities research. Our CBPR partnership pilot tested a multicomponent consent process that provides participants the option to control the use of their data. Consent forms used concise plain language to describe study information, including participant requirements, risks, and personal health information protections, and were available in both English and Marshallese. This study demonstrates that when provided a multicomponent consent, the vast majority of consenting study participants (89.6%) agreed to all additional options, and only five (10.4%) provided consent for some but not all options. Our description of the development and implementation of a multicomponent consent using a CBPR approach adds a specific example of community engagement and may be informative for other indigenous populations.

Publisher

SAGE Publications

Subject

Communication,Education,Social Psychology

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