Literature DB >> 29304939

Standards for Instrument Migration When Implementing Paper Patient-Reported Outcome Instruments Electronically: Recommendations from a Qualitative Synthesis of Cognitive Interview and Usability Studies.

Willie Muehlhausen1, Bill Byrom2, Barbara Skerritt1, Marie McCarthy1, Bryan McDowell3, Jeremy Sohn3.   

Abstract

OBJECTIVES: To synthesize the findings of cognitive interview and usability studies performed to assess the measurement equivalence of patient-reported outcome (PRO) instruments migrated from paper to electronic formats (ePRO), and make recommendations regarding future migration validation requirements and ePRO design best practice.
METHODS: We synthesized findings from all cognitive interview and usability studies performed by a contract research organization between 2012 and 2015: 53 studies comprising 68 unique instruments and 101 instrument evaluations. We summarized study findings to make recommendations for best practice and future validation requirements.
RESULTS: Five studies (9%) identified minor findings during cognitive interview that may possibly affect instrument measurement properties. All findings could be addressed by application of ePRO best practice, such as eliminating scrolling, ensuring appropriate font size, ensuring suitable thickness of visual analogue scale lines, and providing suitable instructions. Similarly, regarding solution usability, 49 of the 53 studies (92%) recommended no changes in display clarity, navigation, operation, and completion without help. Reported usability findings could be eliminated by following good product design such as the size, location, and responsiveness of navigation buttons.
CONCLUSIONS: With the benefit of accumulating evidence, it is possible to relax the need to routinely conduct cognitive interview and usability studies when implementing minor changes during instrument migration. Application of design best practice and selecting vendor solutions with good user interface and user experience properties that have been assessed in a representative group may enable many instrument migrations to be accepted without formal validation studies by instead conducting a structured expert screen review.
Copyright © 2018 International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  PRO; cognitive interview; ePRO; electronic patient-reported outcomes; measurement equivalence; patient-reported outcomes

Mesh:

Year:  2017        PMID: 29304939     DOI: 10.1016/j.jval.2017.07.002

Source DB:  PubMed          Journal:  Value Health        ISSN: 1098-3015            Impact factor:   5.725


  3 in total

1.  Evaluation of the Paper and Smartphone Versions of the Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR16) and the Patient Health Questionnaire-9 (PHQ-9) in Depressed Patients in China.

Authors:  Long Zhen; Gang Wang; Gailing Xu; Le Xiao; Lei Feng; Xu Chen; Man Liu; Xuequan Zhu
Journal:  Neuropsychiatr Dis Treat       Date:  2020-04-17       Impact factor: 2.570

2.  Mobile App-based documentation of patient-reported outcomes - 3-months results from a proof-of-concept study on modern rheumatology patient management.

Authors:  Jutta G Richter; Christina Nannen; Gamal Chehab; Hasan Acar; Arnd Becker; Reinhart Willers; Dörte Huscher; Matthias Schneider
Journal:  Arthritis Res Ther       Date:  2021-04-19       Impact factor: 5.156

3.  Cultural Adaptation and Validation of the Quality of Dying in Long-Term Care Scale (QoD-LTC) for Spanish Nursing Homes.

Authors:  Daniel Puente-Fernández; Rosel Jimeno-Ucles; Emilio Mota-Romero; Concepción Roldán; Katherine Froggatt; Rafael Montoya-Juárez
Journal:  Int J Environ Res Public Health       Date:  2021-05-16       Impact factor: 3.390

  3 in total

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