Insights from the Development of a Dynamic Consent Platform for the ATHENA Program (Preprint)

Author:

Xiong EddyORCID,Bonner CarissaORCID,King AmandaORCID,Bourne ZoltanORCID,Morgan MarkORCID,Tolosa M. XimenaORCID,Stanton TonyORCID,Greaves KimORCID

Abstract

BACKGROUND

Dynamic Consent (DC) resolves many of the issues facing traditional paper-based or electronic consent including providing truly informed and engaged participants in the decision-making process. The Australians Together Health Initiative (ATHENA) Program aims to connect participants across Queensland, Australia with new research opportunities. At its core is the DC platform, an interactive and participant centric digital platform enabling users to view ongoing research activities, update consent preferences, and receive real-time feedback on research outcomes.

OBJECTIVE

To describe the development process, construction, features, and testing of the ATHENA DC platform.

METHODS

One-on-one interviews were undertaken with consumers followed by a workshop with key stakeholders to gain insights on the DC concept. Five problem statements were developed and solutions posed, from which a DC platform was constructed, tested, and used to recruit to a clinical trial. Feedback on user platform experience was gained from a survey hosted on the platform.

RESULTS

Participants were positive about DC, valuing privacy, ease of use and adequate communication. Motivators for registration were feedback on data usage and its broader community benefits. Problem statements were security, trust and governance, ease of use, communication, control, and need for a scalable platform. Using the newly constructed DC platform, 99 participants were recontacted, of whom 59 logged on indicating use, and 22 registered for the clinical trial. Survey feedback was positive, reflecting satisfaction with clarity, brevity, and flexibility of the platform. Key barriers to implementation include technological and health literacy.

CONCLUSIONS

This study outlines the successful development and testing of a DC platform which was well-accepted, with users recognising its advantages over traditional methods of consent regarding flexibility, ease of communication, and participant satisfaction. This information may be useful to others who plan to use DC in healthcare research.

CLINICALTRIAL

NA

Publisher

JMIR Publications Inc.

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