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dc.contributor.authorMaramba, Inocencio Daniel
dc.contributor.authorChatterjee, Arunangsu
dc.date.accessioned2022-03-18T13:49:38Z
dc.date.available2022-03-18T13:49:38Z
dc.date.issued2022-01-06
dc.identifier.issn2563-6316
dc.identifier.issn2563-6316
dc.identifier.othere31679
dc.identifier.urihttp://hdl.handle.net/10026.1/18953
dc.description.abstract

<jats:sec> <jats:title>Background</jats:title> <jats:p>Anesthetic preoperative assessment (POA) is now a common part of the surgical care pathway, and guidelines support its routine use. MyPreOp (Ultramed Ltd) is a web-based POA system that enables remote assessments. Usability is a key factor in the success of digital health solutions.</jats:p> </jats:sec> <jats:sec> <jats:title>Objective</jats:title> <jats:p>This study aims to assess the usability of the MyPreOp system through patient feedback, investigate the amount of time it took for patients to complete the POA questionnaire and the factors that influenced completion time, and explore the effect on completion times of implementing a validated eHealth usability scale, as compared to using a simple but unvalidated usability evaluation scale, and to test the feasibility of administering a more detailed usability evaluation scale in a staggered manner so as not to unduly increase completion times.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>In this cross-sectional study, anonymized data sets were extracted from the MyPreOp system. The participants were adults (aged ≥18 years), scheduled for nonurgent surgical procedures performed in hospitals in the United Kingdom, who gave consent for their anonymized data to be analyzed. Data collected included age, gender, American Society of Anesthesiology (ASA) physical classification status, and completion time. Two user experience evaluations were used: in Phase 1, 2 questions asking about overall experience and ease of use, and in Phase 2, a previously validated usability questionnaire, with its 20 questions equally distributed among 5 succeeding patient cohorts. There were 2593 respondents in total (Phase 1: n=1193; Phase 2: n=1400). The median age of the participants was 46 years, and 1520 (58.62%) of the 2593 respondents were female. End points measured were the median completion times in Phase I and Phase II. The data were collected by extracting a subset of records from the database and exported to a spreadsheet for analysis (Excel, Microsoft Corporation). The data were analyzed for differences in completion times between Phase I and Phase II, as well as for differences between age groups, genders, and ASA classifications.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>MyPreOp scored well in usability in both phases. In Phase 1, 81.64% (974/1193) of respondents had a good or better experience, and 93.8% (1119/1193) found it easy to use. The usability rating in Phase 2 was 4.13 out of a maximum of 5, indicating high usability. The median completion time was 40.4 minutes. The implementation of the longer usability evaluation scale in Phase 2 did not negatively impact the completion times. Age and ASA physical status were found to be moderately associated with increased completion times.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>MyPreOp rates high in both user experience and usability. The method of dividing the questionnaire into 5 blocks is valid and does not negatively affect completion times. Further research into the factors affecting completion time is recommended.</jats:p> </jats:sec>

dc.format.extente31679-e31679
dc.format.mediumElectronic
dc.languageen
dc.language.isoen
dc.publisherJMIR Publications
dc.subjectdigital health
dc.subjectpreoperative assessment
dc.subjectself-completed patient questionnaires
dc.subjectusability
dc.subjectuser experience
dc.subjectweb-based
dc.titleContinuous User Experience Monitoring of a Patient-Completed Preoperative Assessment System in the United Kingdom: Cross-sectional Study
dc.typejournal-article
dc.typeJournal Article
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37725545
plymouth.issue1
plymouth.volume3
plymouth.publication-statusPublished online
plymouth.journalJMIRx Med
dc.identifier.doi10.2196/31679
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA23 Education
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Health and Community
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeCanada
dcterms.dateAccepted2021-10-19
dc.rights.embargodate2022-3-19
dc.identifier.eissn2563-6316
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.2196/31679
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2022-01-06
rioxxterms.typeJournal Article/Review
plymouth.funderE-Health Productivity & Innovation in Cornwall (EPIC2)::European Regional Development Fund


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