Abstract

BackgroundPresbyopia is a progressive condition that reduces the eye’s ability to focus on near objects with increasing age. After a systematic literature review identified no existing presbyopia-specific patient-reported outcome (PRO) instruments meeting regulatory guidance, a new PRO instrument, the Near Vision Presbyopia Task-based Questionnaire (NVPTQ), was developed.ResultsTo explore the patient experience with presbyopia, concept elicitation interviews were conducted with 20 presbyopic participants. The most frequently reported impacts were difficulty with reading menus/books/newspapers/magazines, reading on a cell phone/caller ID, and reading small print. Based on these results, a task-based PRO instrument (the NVPTQ) was developed instructing participants to complete four near-vision, paper-based reading tasks (book, newspaper, nutrition label, menu) under standardized settings, and subsequently assess their vision-related reading ability and associated satisfaction. The draft NVPTQ was cognitively debriefed with a sample of 20 presbyopes, which demonstrated that most participants interpreted the items as intended and endorsed the relevance of the concepts being assessed. After the qualitative research, the draft instrument was psychometrically tested using data from a Phase 2 study. Based on item-level analyses, all items in the NVPTQ demonstrated expected response option patterns and lacked substantial floor or ceiling effects. The reliability, validity, and responsiveness of the NVPTQ Performance and Satisfaction domain scores were assessed. All domains scores had large Cronbach’s coefficient α values and good test–retest statistics, indicating that the scores are internally consistent and produce stable values over time. The pattern of correlations with a concurrent measure of visual functioning (National Eye Institute Visual Function Questionnaire 25) demonstrated that the NVPTQ domain scores were related to an alternative assessment of near-vision activities. The NVPTQ domain scores were able to distinguish between groups that were known to differ on the clinical outcome of uncorrected near visual acuity, supporting the construct validity of these scores. The NVPTQ domain scores showed evidence of responsiveness to change by being able to distinguish between groups defined as improved and not improved based on patient-reported and clinical outcomes.ConclusionsThis research has resulted in a content-valid and psychometrically sound instrument designed to evaluate vision-related reading ability and satisfaction with vision-related reading ability.Trial registration: ClinicalTrials.gov NCT02780115. Registered 23 May 2016, https://www.clinicaltrials.gov/ct2/show/NCT02780115?term=NCT02780115&draw=2&rank=1.

Highlights

  • Presbyopia is a progressive condition that reduces the eye’s ability to focus on near objects with increasing age

  • Presbyopia is an age-related progressive visual condition characterized by the loss of the ability of the eye to focus on near objects

  • Concept elicitation (CE) interviews were planned to inform the development of a new patient-reported outcome (PRO) instrument assessing near-vision reading ability

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Summary

Introduction

Presbyopia is a progressive condition that reduces the eye’s ability to focus on near objects with increasing age. After a systematic literature review identified no existing presbyopia-specific patient-reported outcome (PRO) instruments meeting regulatory guidance, a new PRO instrument, the Near Vision Presbyopia Task-based Questionnaire (NVPTQ), was developed. Presbyopia is an age-related progressive visual condition characterized by the loss of the ability of the eye to focus on near objects. Several patient-reported outcome (PRO) instruments have been utilized to measure the functioning aspects of living with presbyopia, including the National Eye Institute Visual Functioning Questionnaire-25 (NEI VFQ-25) [3, 4], National Eye Institute Refractive Error Quality of Life Instrument-42 (NEI RQL-42) [4, 5], and Near Activity Visual Questionnaire (NAVQ) [6]. None meet the standards in the FDA’s PRO Guidance due to inadequate documentation of content validity, insufficient psychometric measurement properties, and a lack of item content relevance to presbyopia symptoms and impacts [7,8,9]

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