Young people’s preferences on governance models of mental health data: Qualitative study in the UK (Preprint)

Author:

Carey Emma GraceORCID,Adeyemi Faith Oluwasemilore,Neelakantan Lakshmi,Fernandes BlossomORCID,Fazel Mina,Ford Tamsin Jane,Burn Anne-MarieORCID,

Abstract

BACKGROUND

Improving access to mental health data to accelerate research and improve mental health outcomes is a potentially achievable goal given the substantial data that can now be collected from mobile devices. Smartphones can provide a useful mechanism for collecting mental health data from young people, especially as their use is relatively ubiquitous in high-resource settings such as the UK and they have a high capacity to collect active and passive data. This raises the interesting opportunity of establishing a large bank of mental health data from young people, which could be accessed by researchers globally but it is important to clarify how to ensure this is done in an appropriate manner, aligned with the values of young people.

OBJECTIVE

In this study, we discuss the preferences of young people in the UK regarding the governance, sharing and use of their mental health data, with the establishment of a global databank in mind. We aimed to determine whether young people want and feel safe to share their mental health data, if so with whom, and their preferences in doing so.

METHODS

Young people were provided with two modules of educational material about data governance models and background about scientific research. We then conducted 2-hour focus groups, each with 2-7 participants, employing a deliberative democracy methodology to reach a consensus where possible. Findings were analysed using the framework method.

RESULTS

Young people were generally enthusiastic about contributing data to mental health research. They believed that broader availability of mental health data could be used to discover what improves or worsens mental health and to develop new services to support young people. However, this enthusiasm came with many concerns and caveats, including distributed control of access to ensure appropriate use, distributed power, and data management that included diverse representation and sufficient ethical training for applicants and data managers.

CONCLUSIONS

Although it is feasible to use smartphones to collect mental health data from young people in the UK, it is essential to carefully consider the parameters of such a databank. Addressing and embedding young people’s preferences, including the need for robust procedures regarding how their data is managed, stored and accessed will set a solid foundation to establishing any global databank.

Publisher

JMIR Publications Inc.

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