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Evaluating the Forward with Dementia Campaign in Five Countries

Published online by Cambridge University Press:  02 February 2024

Isabelle Vedel
Affiliation:
Department of Family Medicine, McGill University
Shelley Doucet
Affiliation:
Centre for Research in Integrated Care, University of New Brunswick Saint John
Alison Luke
Affiliation:
Centre for Research in Integrated Care, University of New Brunswick Saint John
Carrie McAiney
Affiliation:
University of Waterloo
Pam Jarrett
Affiliation:
Horizon Health Network
Laura Rojas-Rozo
Affiliation:
Department of Family Medicine, McGill University
Amy E. Reid
Affiliation:
Centre for Research in Integrated Care, University of New Brunswick Saint John
Emma Conway
Affiliation:
University of Waterloo
Ana Saavedra
Affiliation:
Department of Family Medicine, McGill University
Luke MacNeill
Affiliation:
Centre for Research in Integrated Care, University of New Brunswick Saint John
Julia Besner
Affiliation:
University of New Brunswick Saint John
Rachel Thombs
Affiliation:
University of New Brunswick Saint John
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Abstract

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Objective:

The Forward with Dementia (FWD) project is a dementia awareness campaign that was implemented across five countries. The campaign included components such as websites (in four languages – www.forwardwithdementia.org), webinars, newsletters, and social media posts. This campaign is the fourth phase of a three-year longitudinal mixed methods study with five phases in five countries: Canada (New Brunswick, Ontario, Quebec), Australia, the Netherlands, United Kingdom, and Poland. The purpose of this study is to evaluate the implementation and perceived impact of the FWD websites and campaign in the five participating countries.

Methods:

The RE-AIM framework (Reach, Effectiveness, Adoption, Implementation, Maintenance) was used to guide the campaign evaluation. The evaluation was drawn from Google Analytics, surveys, individual interviews, and report cards. Data collection occurred between September 2021 and May 2022.

Results:

There were approximately 124,945 page views across all FWD websites during the campaign. Participants of the surveys and interviews reported engaging in a range of campaign activities. They read information about receiving a diagnosis, stories from persons with lived experience in dementia, news, and attended webinars (or watched recording). Most participants rated the information that they read on the website moderately, very, or extremely helpful. In addition, the majority of respondents said that they plan to visit the website again. During the interviews, participants shared that the website was easy to navigate, practical, and that it maintains a positive tone related to dementia. The co-design aspect of the campaign was considered a strength.

Conclusion:

The findings indicate that the FWD campaign can provide support for people who have recently received a dementia diagnosis and their family or friends. In addition, the campaign may provide health and social care providers with a new source of information and tools to use and share with their clients. These results informed the development of a playbook to guide regions and countries beyond those involved in this project to implement similar initiatives.

Type
Symposia
Copyright
© International Psychogeriatric Association 2024

Footnotes

Word Count: 317/350