Evidence map›Paper›PMID 37657840›Full record

ArticleBMJ open2023

Feasibility, comprehensibility and acceptability of the VISION-Cog, a novel tool to assess cognitive impairment in visually impaired older adults: a cross-sectional pilot study in Singapore.

Tai Anh Vu, Eva Fenwick, Kinjal Doshi, Preeti Gupta, Shin Yi Quek, Christopher Chen, Simon Ting, Adeline S L Ng, Philip Yap, Donald Yeo and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 41% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

12 authors at 8 institutions in 3 countries.

Tai Anh VuHealth Services and Systems Research, Duke-NUS Medical School, Singapore.
Eva FenwickHealth Services and Systems Research, Duke-NUS Medical School, Singapore.
Kinjal DoshiDepartment of Psychology, National University of Singapore, Singapore.
Preeti GuptaHealth Services and Systems Research, Duke-NUS Medical School, Singapore.
Shin Yi QuekDepartment of Psychology, Ng Teng Fong General Hospital, Singapore.
Christopher ChenDepartments of Pharmacology and Psychological Medicine, National University of Singapore, Singapore.
Simon TingDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Adeline S L NgDepartment of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Philip YapDepartment of Geriatric Medicine, Khoo Teck Puat Hospital, Singapore.
Donald YeoKALL Psychological & Counselling Services Pte Ltd, Singapore.
Dan MileaHealth Services and Systems Research, Duke-NUS Medical School, Singapore.
Ecosse LamoureuxHealth Services and Systems Research, Duke-NUS Medical School, Singapore ecosse.lamoureux@duke-nus.edu.sg.
Duke-NUS Medical School · SGNational University of Singapore · SGTan Tock Seng Hospital · SGFondation de Rothschild · FRKhoo Teck Puat Hospital · SGNg Teng Fong General Hospital · SGSingapore Eye Research Institute · SGThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe pilot-tested the

designThe VISION-Cog was iteratively fine-tuned through pilot studies and expert-panel discussion. In the first pilot study (Stage 1), we recruited 15 visually impaired and cognitively normal participants aged ≥60 years to examine the pilot VISION-Cog's feasibility (length of time to administer), comprehensibility (clarity of instructions) and acceptability (participant burden). We then presented the pilot results to the expert panel (Stage 2) who decided via agreement on a revised version of the VISION-Cog. Subsequently, we conducted a second pilot study (Stage 3) on another four participants to ascertain improvement in feasibility, comprehensibility and acceptability of the revised version.

settingSingapore Eye Research Institute.

participantsNineteen Asian adults aged ≥60 years with visual impairment (defined as near visual acuity worse than N8) were recruited. OUTCOME MEASURE: Revised VISION-Cog.

resultThe VISION-Cog was deemed feasible, taking approximately 60 min to complete on average. All participants agreed that the test instructions were clear, and the battery did not cause undue discomfort or frustration. The data collector rated all tests as very user-friendly (score of 5/5). Minor modifications to the pilot VISION-Cog were suggested by the panel to improve its safety, clarity of instructions and content validity, which were incorporated and iteratively tested in the second pilot study until no further issues emerged.

conclusionsUsing an iterative mixed-methods process, we have developed a feasible, comprehensible and acceptable 5-domain and 9-item visually independent VISION-Cog test battery suitable to assist CI diagnosis in older adults with visual impairment. We will assess its diagnostic potential against clinician-based assessment of CI in subsequent phases.

Indexed as

Cognitive DysfunctionVision, LowAgedCross-Sectional StudiesFeasibility StudiesHumansPilot ProjectsSingaporedelirium & cognitive disordersdementianeurologyneuro-ophthalmologyold age psychiatry

Identifiers

PMID37657840
PMCPMC10476112
OpenAlexW4386366435

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

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.