ArticleImplementation science communications2026
Walking the talk for dementia: building social networks and collaborations.
Article in Implementation science communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- The scope and impact of Walking the Talk for Dementia 2024.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundDementia is one of the greatest global health challenges requiring multimodal efforts to address its impact on people and societies. Walking the Talk for Dementia (WTD) is a unique global initiative designed to challenge the stigma that surrounds dementia, foster intergenerational dialogue, build a community, and inspire a renewed sense of purpose among participants. A social network analysis (SNA) was conducted to provide greater detail and contextualization of the connections made during WTD and insights into the collaborations that arose from this immersive event which may influence dementia policy, care, and services.
methodsA robust, comprehensive, and minimally intrusive evaluation was created in 2024 to capture the results, outcomes, and impacts of WTD 2024. This mixed methods research examined the experiences of the WTD 2024 participants, 79 of whom consented to participate in this research. Pre- and post-surveys collected quantitative and qualitative data (94% and 87% response rates), and were augmented by 95 written, audio, or video reflections. To further investigate the social network of the larger WTD community, a follow-up survey was sent six months after WTD 2024 to the 2024 participants plus the additional 40 participants from WTD 2023. Quantitative survey data were analyzed with descriptive and inferential statistics; qualitative data were analyzed using content analysis to identify core aspects and common themes of the experience. A social network analysis (SNA) was used to visualize and quantify connections between participants of WTD.
resultsResults from the SNA analyses illustrate the development of multiple new connections and collaborations among WTD participants. The results also point to how connections and collaborations among participants that existed prior to WTD 2024 may have changed as a result of WTD.
conclusionsConnections appear to have increased post-WTD. A community developed among WTD participants, who are a multi-disciplinary, global group of professionals and people with lived experience of dementia. This analysis provides evidence of the benefits of social connections for individuals living with dementia and their care partners with other dementia advocates. These findings are important to future advancement of dementia awareness, advocacy, and policy change.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.