Background: Dementia misconceptions on social media are common, with negative effects on people with the condition, their carers, and those who know them. This study codeveloped a thematic framework with carers to understand the forms these misconceptions take on Twitter.
Objective: The aim of this study is to identify and analyze types of dementia conversations on Twitter using participatory methods.
Methods: A total of 3 focus groups with dementia carers were held to develop a framework of dementia misconceptions based on their experiences. Dementia-related tweets were collected from Twitter's official application programming interface using neutral and negative search terms defined by the literature and by carers (N=48,211). A sample of these tweets was selected with equal numbers of neutral and negative words (n=1497), which was validated in individual ratings by carers. We then used the framework to analyze, in detail, a sample of carer-rated negative tweets (n=863).
Results: A total of 25.94% (12,507/48,211) of our tweet corpus contained negative search terms about dementia. The carers' framework had 3 negative and 3 neutral categories. Our thematic analysis of carer-rated negative tweets found 9 themes, including the use of weaponizing language to insult politicians (469/863, 54.3%), using dehumanizing or outdated words or statements about members of the public (n=143, 16.6%), unfounded claims about the cures or causes of dementia (n=11, 1.3%), or providing armchair diagnoses of dementia (n=21, 2.4%).
Conclusions: This is the first study to use participatory methods to develop a framework that identifies dementia misconceptions on Twitter. We show that misconceptions and stigmatizing language are not rare. They manifest through minimizing and underestimating language. Web-based campaigns aiming to reduce discrimination and stigma about dementia could target those who use negative vocabulary and reduce the misconceptions that are being propagated, thus improving general awareness.
Keywords: Alzheimer’s Disease; Twitter; co-production; dementia; misconceptions; patient and public involvement; social media; stigma.
©Georgie Hudson, Sonja M Jansli, Sinan Erturk, Daniel Morris, Clarissa M Odoi, Angela Clayton-Turner, Vanessa Bray, Gill Yourston, Doreen Clouden, David Proudfoot, Andrew Cornwall, Claire Waldron, Til Wykes, Sagar Jilka. Originally published in JMIR Aging (https://aging.jmir.org), 24.01.2022.