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How does the subjective well-being of Australian adults with a congenital corpus callosum disorder compare with that of the general Australian population?

Crossref DOI link: https://doi.org/10.1007/s11136-024-03741-w

Published Online: 2024-07-24

Published Print: 2024-11

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Maxfield, Maree https://orcid.org/0000-0002-7654-494X
McVilly, Keith https://orcid.org/0000-0002-9753-9031
Devine, Alexandra https://orcid.org/0000-0002-7549-9876
Davey, Christian https://orcid.org/0000-0003-3097-9769
Jordan, Helen https://orcid.org/0000-0002-4136-8608
Funding

Funding for this research was provided by:

University of Melbourne
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Text and Data Mining valid from 2024-07-24

Version of Record valid from 2024-07-24
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Article History

Accepted: 14 July 2024

First Online: 24 July 2024

Declarations

:

: This study was performed in line with the Principles of the Declaration of Helsinki. Ethics approval (Ref. 2021-20393-19867-3) was granted by the the Human Research Ethics Committee (HREC) of The University of Melbourne on July 19, 2021.

: The authors confirm that informed consent, including publication, was gained from all individual participants in the study. Participants were provided with options of standard and ‘Easy English’ written Plain Language Statements (PLS) in addition to a verbal version of the PLS.

: The authors have no relevant financial or non-financial interests to disclose.

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