ArticleJournal of Alzheimer's disease : JAD2025
Carers' recognition of concurrent visual impairment in dementia.
Article in Journal of Alzheimer's disease : JAD, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background40-60% of people with dementia live with visual impairment. Those with mild-moderate dementia reliably report reduced vision-related quality of life across several visual domains with associated effects on vision-related social functioning. Despite the marked impact on concurrent dementia and visual impairment, no studies have investigated whether the impact of visual impairment on the lived experiences of people with dementia is recognised by their carers.ObjectiveThe present study investigated whether: (1) problems related to vision and vision-related quality of life reported by people with dementia are recognised and acknowledged by their carers and (2) whether currently validated vision-related quality of life measures for mild-moderate dementia are appropriate as proxy measures of vision-related quality of life in this group.MethodsThe 25-item National Eye Institute Visual Function Questionnaire (NEI VFQ-25) and the Visual Activities Questionnaire (VAQ) were completed by 48 participants with mild-moderate dementia and 48 carers. Participants with dementia completed the questionnaires based on their own experiences and carers completed them by proxy (i.e., on behalf of the person with dementia for whom they cared).ResultsThere was good agreement between people with dementia and their carers on both measures overall and on the majority of subscales, with no significant differences between carer and dementia reports.ConclusionsThis provides further support that people with mild-moderate dementia can accurately report their visual experiences, and that carers could provide a valid proxy of the existence and impact of visual impairment on people living with dementia.
Indexed as
Identifiers
What OpenQuestion holds
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.