Evidence map›Paper›PMID 41609970›Full record

ArticleJournal of patient-reported outcomes2026

Assessing patient engagement approaches in the development of patient reported outcome measures.

Farheen Khan, Michelle Prunier, Ivana Ristevski, Maja Trantalovski, Helen Dimaras

Abstract read
In one paragraph

Article in Journal of patient-reported outcomes, 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

5 authors.

Farheen KhanDepartment of Ophthalmology and Vision Sciences, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, M5G 1X8, Canada.
Michelle PrunierPatient Partner, The Hospital for Sick Children, Toronto, Ontario, Canada.
Ivana RistevskiPatient Partner, The Hospital for Sick Children, Toronto, Ontario, Canada.
Maja TrantalovskiPatient Partner, The Hospital for Sick Children, Toronto, Ontario, Canada.
Helen DimarasDepartment of Ophthalmology and Vision Sciences, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, M5G 1X8, Canada. helen.dimaras@sickkids.ca.ORCID http://orcid.org/0000-0003-1164-2001

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGuidelines for the development and validation of patient-reported outcome measures recommend incorporating patient input to ensure relevance and comprehension, but do not clearly define what patient input entails. As a result, meaningful patient engagement is often conflated with research participation. This study uses the adaptation and validation of the FACE-Q Craniofacial Module patient-reported outcome measure for ophthalmology patients as a case study to showcase how patients can be engaged as partners across the different phases of patient-reported outcome measure adaptation, and illustrate how their involvement influenced the adaptation process.

methodsPatient engagement strategies across five phases of the adaptation and validation of the FACE-Q Craniofacial Module (Study development, Item adaptation, Item reduction, Psychometric evaluation, and Dissemination) were retrospectively mapped to the International Association for Public Participation Spectrum. This framework outlines five levels of engagement: Inform, Consult, Involve, Collaborate, and Empower, and was used to evaluate the extent and nature of engagement.

resultsPatient partners (n = 8) with lived experience of retinoblastoma, strabismus, corneal anesthesia, and ocular prostheses were engaged across the five phases of the study. Mapping engagement activities to the International Association for Public Participation Spectrum revealed that the “Inform” and “Involve” levels of engagement were present in all five phases. The most extensive engagement, spanning all levels of the International Association for Public Participation Spectrum, occurred during the “Item Reduction” and “Dissemination” phases of the study.

conclusionThe current case study showcases that patient engagement can be incorporated intentionally across all phases of patient-reported outcome measure adaptation and validation. The International Association for Public Participation Spectrum provided a structured approach to map and document the nature and extent of engagement across our study. Our case study may support the planning, execution, and reporting of patient engagement strategies in future patient-reported outcome measure development and adaptation studies.

Indexed as

Patient ParticipationPatient Reported Outcome MeasuresAdultFemaleHumansMalePsychometricsReproducibility of ResultsRetrospective StudiesSurveys and Questionnaires

Identifiers

PMID41609970
PMCPMC12923710

What Socratic holds

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LicenceCC BY
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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 Socratic graph.