Hostname: page-component-7bb8b95d7b-lvwk9 Total loading time: 0 Render date: 2024-10-04T16:20:19.082Z Has data issue: false hasContentIssue false
  • English
  • Français

Fear of Dementia and the Obligation to Provide Aggregate Research Results to Study Participants—ADDENDUM

Published online by Cambridge University Press:  24 February 2023

Mackenzie Graham ,
Francesca Farina ,
Craig W. Ritchie ,
Brian Lawlor  and
Lorina Naci
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content. As you have access to this content, full HTML content is provided on this page. A PDF of this content is also available in through the ‘Save PDF’ action button.
Type
Addendum
Information
Cambridge Quarterly of Healthcare Ethics , Volume 32 , Issue 2 , April 2023 , pp. 306
Copyright
© The Author(s), 2023. Published by Cambridge University Press

In the article by Graham et al.,Footnote 1 a funding statement was omitted. The funding statement should read as follows:

Funding Statement

FF is funded by an International Research Fellowship from the Alzheimer’s Association (AARF-21-848281) and a Pilot Award for Leaders in Brain Health from the Global Brain Health Institute, Trinity College Dublin (GBHI ALZ UK-22-863168).

The funding statement has been added to the online version of the article.

References

1 Graham M, Farina F, Ritchie CW, Lawlor B, Naci L. Fear of dementia and the obligation to provide aggregate research results to study participants. Cambridge Quarterly of Healthcare Ethics 2022;31(4):498-505. https://doi.org/10.1017/S0963180122000408.