Evidence map›Paper›PMID 41920390›Full record

ArticleQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation2026

Carers' interpretation of the recall period and perspective-taking when completing the EQ health and wellbeing instrument (EQ-HWB)-9 as proxies for people with dementia: a think-aloud study.

Carrie-Anne Ng, Kathleen Doherty, Margo Bryan, Jill Carlton, Tim Luckett, Brendan Mulhern, Richard Norman, Karen Wills, Jessica Roydhouse

Abstract read
In one paragraph

Article in Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Carrie-Anne NgCentre for Health Economics Research and Evaluation, University of Technology Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0001-9326-8492
Kathleen DohertyWicking Dementia Research and Education Centre, University of Tasmania, Hobart, TAS, Australia.ORCID http://orcid.org/0000-0002-0122-0123
Margo BryanLived Experience Partner, Hobart, TAS, Australia.
Jill CarltonSheffield Centre for Health and Related Research, University of Sheffield, Sheffield, UK.ORCID http://orcid.org/0000-0002-9373-7663
Tim LuckettImproving Palliative, Aged and Chronic Care Through Clinical Research and Translation (IMPACCT), Faculty of Health, University of Technology Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0001-6121-5409
Brendan MulhernCentre for Health Economics Research and Evaluation, University of Technology Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0003-3656-8063
Richard NormanSchool of Population Health, Curtin University, Perth, WA, Australia.ORCID http://orcid.org/0000-0002-3112-3893
Karen WillsMenzies Institute for Medical Research, University of Tasmania, 15-17 Liverpool Street, Hobart, TAS, 7000, Australia.ORCID http://orcid.org/0000-0003-3897-2908
Jessica RoydhouseMenzies Institute for Medical Research, University of Tasmania, 15-17 Liverpool Street, Hobart, TAS, 7000, Australia. jessica.roydhouse@utas.edu.au.ORCID http://orcid.org/0000-0002-8025-5841

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePatient-reported outcome measures are often administered with specific recall periods to standardise reporting. However, research on recall periods in proxy reporting is limited. This study sought to explore (1) how informal carers interpret the “last 7 days” recall period of the EQ health and well-being instrument (EQ-HWB)-9 and (2) the perspective they adopt when completing the measure to report on the health and well-being of persons with dementia.

methodsA qualitative, descriptive study was conducted. Convenience sampling was used for recruitment. We interviewed informal carers of persons with dementia in Australia using semi-structured cognitive interviews. Participants were asked to think aloud when completing the EQ-HWB-9, and three additional positively-framed questions from the EQ-HWB. Thematic analysis was used, where transcripts were inductively coded to capture new insights and deductively coded as guided by the EQ-HWB-9 questions.

resultsNineteen carers completed interviews. Carers used two main retrieval strategies: supplementing recent observations with key events or self-report occurring slightly outside the recall period, and drawing on the past to contextualise recent behaviours. All participants used their own observations and opinions of the person with dementia (“proxy–proxy perspective”). When questions about the person’s feelings were difficult to answer, carers relied on various observable behaviours as indirect indicators. Nearly half also imagined how the person might answer (“proxy–patient perspective”), even if they sometimes disagreed with the person’s self-assessment.

conclusionThe 7-day recall period for the EQ-HWB-9 was more consistently adhered to for observable aspects of health. Wording changes may be needed to support consistent use, particularly for less observable items. Challenges in perspective-taking and adherence were also identified, suggesting areas to address in instructions.

Indexed as

CaregiversDementiaMental RecallPatient Reported Outcome MeasuresProxyQuality of LifeAgedAged, 80 and overAustraliaFemaleHumansInterviews as TopicMaleMiddle AgedPsychological Well-BeingQualitative ResearchDementiaPerspectiveProxyRecallWell-being

Identifiers

PMID41920390
PMCPMC13043530

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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.