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Home Data Collection

Solutions to COVID-19 data sharing

globalresearchsyndicate by globalresearchsyndicate
December 2, 2020
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We read with interest The Lancet Digital Health Editorial regarding transparency during global health emergencies, and we wanted to bring to your readers’ attention our work on data sharing.

1

The Lancet Digital Health
Transparency during global health emergencies.

After WHO’s declaration of COVID-19 as a global pandemic, the COVID-19 Clinical Research Coalition was established on April 2, 2020.

2

COVID-19 Clinical Research Coalition
Global coalition to accelerate COVID-19 clinical research in resource-limited settings.

The Coalition is made up of global health researchers working in, or allied with, resource-limited settings across multiple continents. This umbrella group has grown, with working groups now spanning nearly a dozen interest areas including ethics, clinical pharmacology, and data sharing. Here, we outline the rationale and aims of the Data Sharing Working Group, which comprises researchers working on ethics, regulatory, and operational aspects of data sharing.

As the Editorial highlighted, the importance of promoting effective, ethical, and equitable data sharing has increased in the time of COVID-19. International funders such as the Wellcome Trust

3

Wellcome Trust
Sharing research data and findings relevant to the novel coronavirus (COVID-19) outbreak.

and the Bill & Melinda Gates Foundation have mandated that funding recipients share data from research related to COVID-19 as soon as the study is completed, regardless of publication status. However, the challenges of data sharing persist. These include complexities of broad consent, lack of data management capacity, and the potential for exacerbating existing inequalities between researchers in low-resource and high-resource settings.

4

  • Bull S
  • Cheah PY
  • Denny S
  • et al.
Best practices for ethical sharing of individual-level health research data from low- and middle-income settings.

, 

5

  • Cheah PY
  • Jatupornpimol N
  • Hanboonkunupakarn B
  • et al.
Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand.

Based on our observations, although many journals require a data sharing statement, mechanisms for accessing individual participant data are seldom provided by the authors of published COVID-19 trials, and data sharing defaults to interested investigators contacting authors to inquire about data acquisition.

Given the public health imperative to share data to accelerate effective COVID-19 responses, the Data Sharing Working Group was convened to facilitate and promote effective, ethical, and equitable data sharing across geographies and disciplines. Specifically, the Data Sharing Working Group synthesises existing policies, guidance, and good practice on data sharing by funders, journals, and practitioners; and provides practical advice to researchers and data management teams on data sharing, including recommended language for broad consent for secondary use of data, recommendations for selecting repositories or platforms for data sharing, guidance on governance for data sharing, and recommendations for developing data access agreements. We aim to promote the greatest use possible of the data generated to help with the management of the pandemic, while protecting the interests of study participants, their communities, and the researchers who generated the data.

We encourage researchers who are seeking practical solutions to data sharing to contact us ([email protected]).

We declare no competing interests.

Supplementary Material

References

  1. 1.
    • The Lancet Digital Health

    Transparency during global health emergencies.

    Lancet Digit Health. 2020; 2: e441

  2. 2.
    • COVID-19 Clinical Research Coalition

    Global coalition to accelerate COVID-19 clinical research in resource-limited settings.

    Lancet. 2020; 395: 1322-1325

  3. 3.

    Sharing research data and findings relevant to the novel coronavirus (COVID-19) outbreak.

  4. 4.
    • Bull S
    • Cheah PY
    • Denny S
    • et al.

    Best practices for ethical sharing of individual-level health research data from low- and middle-income settings.

    J Empir Res Hum Res Ethics. 2015; 10: 302-313

  5. 5.
    • Cheah PY
    • Jatupornpimol N
    • Hanboonkunupakarn B
    • et al.

    Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand.

    BMC Med Ethics. 2018; 19: 86

Article Info

Publication History

Published: December 01, 2020

Identification

DOI: https://doi.org/10.1016/S2589-7500(20)30273-9

Copyright

© 2020 Elsevier Ltd.

User License

Creative Commons Attribution (CC BY 4.0) |

ScienceDirect

Access this article on ScienceDirect

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