Evidence map›Paper›PMID 42640161›Full record

ArticleTranslational vision science & technology2026

A Within-Population Comparison of the Psychometric Properties and Clinical Feasibility of Visual Function Questionnaires in Low Vision.

Micaela Gobeille, Nicole Ross, Chris Bradley

Abstract readComparative Study
In one paragraph

Article in Translational vision science & technology, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Micaela GobeilleNew England College of Optometry, Department of Specialty Care and Vision Science, Boston, MA, USA.
Nicole RossNew England College of Optometry, Department of Specialty Care and Vision Science, Boston, MA, USA.
Chris BradleyJohns Hopkins University School of Medicine, Baltimore, MD, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The purpose of this study was to determine which of three visual function questionnaires (VFQs) is most appropriate and practical for low vision (LV) clinical use when administered to the same LV patient sample. Methods: Activity Inventory goals (AI-G), Veterans Affairs Low-Vision Visual Functioning Questionnaire 48 (VA LV VFQ-48), and National Eye Institute Visual Function Questionnaire 25 visual function subscale (NEI VFQ-25c-VF) were administered to 74 patients with LV pre- and 6 months post-LV examination. Rasch analysis estimated person measures, item measures, and infit mean square statistics (infits). Targeting was assessed using the Kolmogorov-Smirnov (KS) test, while Deming regression and Pearson correlation tests compared person measures between VFQs and between pre- and post-LV examination. The Wilcoxon signed-rank test compared administration time per item for a subset (n = 30) of participants. Results: Statistically significant ceiling effects were observed for AI-G and VA LV VFQ-48, but not for NEI VFQ-25c-VF (P = 0.39). However, NEI VFQ-25c-VF had the highest percentage of combined pre- and post-LV person (31.1%) and item (20%) infits beyond a desirable range of 0.5 to 1.5, indicating greater multidimensionality. Person measures were moderately correlated between AI-G and both VA LV VFQ-48 (r = 0.64) and NEI VFQ-25c-VF (r = 0.63), but strongly correlated between NEI VFQ-25c-VF and VA LV VFQ-48 (r = 0.85). Regarding clinical practicality, pre-LV examination administration time per item was significantly faster for VA LV VFQ-48 than for AI-G (P = 0.00016) or NEI VFQ-25c-VF (P = 0.0065). Conclusions: No VFQ was superior in all respects. Although NEI VFQ-25c-VF had the best targeting, its higher multidimensionality supports using VA LV VFQ-48 if patient ability remains below the instrument ceiling. Translational Relevance: Improvements to widely used VFQs are required for use in LV clinics.

Indexed as

PsychometricsVision, LowVisual AcuityAdultAgedAged, 80 and overFeasibility StudiesFemaleHumansMaleMiddle AgedReproducibility of ResultsSurveys and Questionnaires

Identifiers

PMID42640161
PMCPMC13543573

What OpenQuestion holds

Textmetadata
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Registered trials

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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.