Hostname: page-component-848d4c4894-wg55d Total loading time: 0 Render date: 2024-05-23T02:06:11.500Z 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
Get access Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. Please use the Get access link above for information on how to access this content.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
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

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

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.