Standardised data collection from people with dementia over the telephone: A qualitative study of the experience of DETERMIND programme researchers in a pandemic.

data collection dementia person-oriented standardised measures telephone interviews

Journal

Dementia (London, England)
ISSN: 1741-2684
Titre abrégé: Dementia (London)
Pays: England
ID NLM: 101128698

Informations de publication

Date de publication:
Nov 2023
Historique:
medline: 15 11 2023
pubmed: 27 7 2023
entrez: 26 7 2023
Statut: ppublish

Résumé

There is a notable lack of evidence on what constitutes good practice in remote quantitative data collection from research participants with dementia. During the COVID-19 pandemic face-to-face research became problematic, especially where participants were older and more at risk of infection. The DETERMIND-C19 study, a large cohort study of people with dementia, switched to telephone data collection over this period. This paper explores the experiences of researchers who collected quantitative data over the telephone from people with dementia during the first COVID-19 lockdowns in England. The aim was to learn from these experiences, share insights and inform future research practice across disciplines. Seven DETERMIND researchers were interviewed about the processes and challenges of collecting quantitative data from people with dementia over the telephone compared to face-to-face. Data were analysed using reflexive thematic analysis. Two themes were developed: first the telephone adds an extra layer of confusion to an already cognitively complex interaction. Second, researchers found it difficult to recognise subtle cues that signalled participants' rising emotion over the telephone in time to prevent distress. The researchers employed strategies to support participants which may not have conformed to the strict conventions of structured interviewing, but which were informed by person-oriented principles. Whilst in practice this may be a common approach to balancing the needs of participants and the requirements of quantitative research, it is rare for studies to openly discuss such trade-offs in the literature. Honest, reflective reporting is required if the practice of remote data collection from people with dementia is to progress ethically and with integrity.

Identifiants

pubmed: 37495232
doi: 10.1177/14713012231190585
pmc: PMC10372513
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1718-1737

Déclaration de conflit d'intérêts

Declaration of conflicting interestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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Auteurs

Kate Gridley (K)

Social Policy Research Unit, University of York, UK.

Josie Dixon (J)

Care Policy and Evaluation Centre (CPEC), London School of Economics and Political Science, London, UK.

Ben Hicks (B)

Brighton and Sussex Medical School, University of Sussex, UK.

Yvonne Birks (Y)

Social Policy and Social Work, University of York, UK.

Kate Baxter (K)

Social Policy Research Unit, University of York, UK.

Eleanor Miles (E)

School of Psychology, University of Sussex, UK.

Louise Robinson (L)

Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, UK.

Rotem Perach (R)

School of Social Sciences, University of Westminster, UK.

Sube Banerjee (S)

Faculty of Health, University of Plymouth, UK.

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