People with Cerebral Palsy and Their Family’s Preferences about Genomics Research

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dc.contributor.authorWilson, Y.A.
dc.contributor.authorMcIntyre, S.
dc.contributor.authorWaight, E.
dc.contributor.authorThornton, M.
dc.contributor.authorvan Otterloo, S.
dc.contributor.authorMarmont, S.R.
dc.contributor.authorKruer, M.
dc.contributor.authorBaynam, G.
dc.contributor.authorGecz, J.
dc.contributor.authorBadawi, N.
dc.date.issued2022
dc.description.abstractIntroduction: The goal of this study was to understand individuals with cerebral palsy (CP) and their family’s attitudes and preferences to genomic research, including international data sharing and biobanking. Methods: Individuals with CP and their family members were invited to participate in the web-based survey via email (NSW/ACT CP Register) or via posts on social media by Cerebral Palsy Alliance, CP Research Network, and CP Now. Survey responses included yes/no/unsure, multiple choices, and Likert scales. Fisher’s exact and χ2 tests were used to assess if there were significant differences between subgroups. Results: Individuals with CP and their families (n = 145) were willing to participate in genomics research (68%), data sharing (82%), and biobanking efforts (75%). This willingness to participate was associated with completion of tertiary education, previous genetic testing experience, overall higher genomic awareness, and trust in international researchers. The survey respondents also expressed ongoing communication and diverse information needs regarding the use of their samples and data. Major concerns were associated with privacy and data security. Discussion: The success of genomic research and international data sharing efforts in CP are contingent upon broad support and recruitment. Ongoing consultation and engagement of individuals with CP and their families will facilitate trust and promote increased awareness of genomics in CP that may in turn maximize participant uptake and recruitment.
dc.description.statementofresponsibilityYana Alexandra Wilson, Sarah McIntyre, Emma Waight, Marelle Thornton, Saskia van Otterloo, Sophie Rachel Marmont, Michael Kruer, Gareth Baynam, Jozef Gecz, Nadia Badawi
dc.identifier.citationPublic Health Genomics, 2022; 25(1-2):1-10
dc.identifier.doi10.1159/000518942
dc.identifier.issn1662-4246
dc.identifier.issn1662-8063
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]
dc.identifier.urihttps://hdl.handle.net/2440/145824
dc.language.isoen
dc.publisherS. Karger AG
dc.rights© 2021 The Author(s) Published by S. Karger AG, Basel. This is an Open Access article licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense), applicable to the online version of the article only. Usage and distribution for commercial purposes requires written permission
dc.source.urihttps://doi.org/10.1159/000518942
dc.subjectCerebral palsy; Genome research; Participant perspectives; Data sharing; Biobanking
dc.titlePeople with Cerebral Palsy and Their Family’s Preferences about Genomics Research
dc.typeJournal article
pubs.publication-statusPublished

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