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Regulating mobile health research in Canada

Public trust and public participation

Bibliographic Data

ID19571007
AuthorsMa’n H Zawati (0000-0002-8905-6259, McGill University, corresponding author), Michael Lang (0000-0003-3268-215X, McGill University)
Year2024
Volume32
Pages100988
Publication date2024-01-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueEthics Medicine and Public Health (JOURNAL)
Journal identifiersISSN: 2352-5525 • E-ISSN: 2352-5533
PublisherElsevier BV (PUBLISHER)
DOI10.1016/j.jemep.2024.100988
OpenAlexW4396996299
LanguageEN
References cited20

Smartphone applications provide unique opportunities for health research. Prospective participants may be recruited, give consent, and may share personal health information with researchers with unparalleled efficiency. Mobile health apps thus have the potential to profoundly alter the way health research is conducted, thereby contributing to more effective and more equitably distributed clinical interventions. But the regulation of this kind of research is uncertain. The absence of regulatory guidance may limit mobile health's promise. The mobile health research landscape in Canada is considered in the context of the existing regulatory framework, academic literature, and current applications. This paper outlines regulatory issues in the Canadian context, suggesting three key issues to which researchers and regulators ought to be attentive to ensure public trust: consent, return of results, and privacy and security. Further consideration of regulatory and ethical issues is needed if mobile health will earn the public's trust and promote public participation

Business · Political science · Public health · Public participation · Public relations · Public trust · Biomedical Ethics and Regulation · Ethics in Clinical Research · Medicine · Mobile Health and mHealth Applications · Nursing · Public Administration

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