Sunner, Carla
Giles, Michelle
Ball, Jean
Barker, Roslyn
Hullick, Carolyn
Oldmeadow, Christopher
Foureur, Maralyn
Funding for this research was provided by:
NSW Ministry of Health (Translational Research Grant Scheme (H19/53776), Translational Research Grant Scheme (H19/53776), Translational Research Grant Scheme (H19/53776), Translational Research Grant Scheme (H19/53776), Translational Research Grant Scheme (H19/53776), Translational Research Grant Scheme (H19/53776), Translational Research Grant Scheme (H19/53776))
Article History
Received: 11 April 2023
Accepted: 27 November 2023
First Online: 18 December 2023
Declarations
:
: Consent, adhered to the standards and guidelines that align with the ethical approval processes outlined by the Australian National Health and Medical Research Council [CitationRef removed]. The Hunter New England Human Research Ethics Committee (2019/ ETH12853) and University of Newcastle Human Research Ethics Committee (H-2020–0090) approved that individual resident informed and signed consent was waivered in this study given that the intervention was being implemented at facility level and was considered part of usual care and practices (adding a visual augmentation of already existing routine ACE practices). In addition, all individual clinical data was collection, de-identified and reported in accordance with Australian National Health and Medical Research Council [CitationRef removed] and these methods were approved by the Hunter New England Human Research Ethics Committee (2019/ ETH12853) and University of Newcastle Human Research Ethics Committee (H-2020–0090).
: Not applicable.
: The authors have no competing interests to declare that are relevant to the content of this article.