Back to Search Start Over

A REDCap-based model for electronic consent (eConsent): Moving toward a more personalized consent.

Authors :
Lawrence CE
Dunkel L
McEver M
Israel T
Taylor R
Chiriboga G
Goins KV
Rahn EJ
Mudano AS
Roberson ED
Chambless C
Wadley VG
Danila MI
Fischer MA
Joosten Y
Saag KG
Allison JJ
Lemon SC
Harris PA
Source :
Journal of clinical and translational science [J Clin Transl Sci] 2020 Apr 03; Vol. 4 (4), pp. 345-353. Date of Electronic Publication: 2020 Apr 03.
Publication Year :
2020

Abstract

Introduction: The updated common rule, for human subjects research, requires that consents "begin with a 'concise and focused' presentation of the key information that will most likely help someone make a decision about whether to participate in a study" (Menikoff, Kaneshiro, Pritchard. The New England Journal of Medicine . 2017; 376 (7): 613-615.). We utilized a community-engaged technology development approach to inform feature options within the REDCap software platform centered around collection and storage of electronic consent (eConsent) to address issues of transparency, clinical trial efficiency, and regulatory compliance for informed consent (Harris, et al. Journal of Biomedical Informatics 2009; 42 (2): 377-381.). eConsent may also improve recruitment and retention in clinical research studies by addressing: (1) barriers for accessing rural populations by facilitating remote consent and (2) cultural and literacy barriers by including optional explanatory material (e.g., defining terms by hovering over them with the cursor) or the choice of displaying different videos/images based on participant's race, ethnicity, or educational level (Phillippi, et al. Journal of Obstetric, Gynecologic, & Neonatal Nursing . 2018; 47 (4): 529-534.).<br />Methods: We developed and pilot tested our eConsent framework to provide a personalized consent experience whereby users are guided through a consent document that utilizes avatars, contextual glossary information supplements, and videos, to facilitate communication of information.<br />Results: The eConsent framework includes a portfolio of eight features, reviewed by community stakeholders, and tested at two academic medical centers.<br />Conclusions: Early adoption and utilization of this eConsent framework have demonstrated acceptability. Next steps will emphasize testing efficacy of features to improve participant engagement with the consent process.<br />Competing Interests: The authors declare no conflicts of interest.<br /> (© The Association for Clinical and Translational Science 2020.)

Details

Language :
English
ISSN :
2059-8661
Volume :
4
Issue :
4
Database :
MEDLINE
Journal :
Journal of clinical and translational science
Publication Type :
Academic Journal
Accession number :
33244416
Full Text :
https://doi.org/10.1017/cts.2020.30