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dc.contributor.authorGoswami, Pushpendra
dc.contributor.authorOliva, Esther
dc.contributor.authorIonova, Tatyana
dc.contributor.authorElse, R
dc.contributor.authorKell, J
dc.contributor.authorFielding, AK
dc.contributor.authorJennings, DM
dc.contributor.authorKarakantza , M
dc.contributor.authorAl-Ismail, S
dc.contributor.authorLyness, J
dc.contributor.authorCollins, GP
dc.contributor.authorMcConnell , S
dc.contributor.authorLangton, C
dc.contributor.authorAl-Obaidi, MJ
dc.contributor.authorOblak, M
dc.contributor.authorSalek, Mir-Saeed Shayegan
dc.date.accessioned2019-05-09T14:06:02Z
dc.date.available2019-05-09T14:06:02Z
dc.date.issued2019-04-30
dc.identifier.citationGoswami , P , Oliva , E , Ionova , T , Else , R , Kell , J , Fielding , AK , Jennings , DM , Karakantza , M , Al-Ismail , S , Lyness , J , Collins , GP , McConnell , S , Langton , C , Al-Obaidi , MJ , Oblak , M & Salek , M-S S 2019 , ' Paper and electronic versions of HM-PRO, a novel patient-reported outcome measure for hematology: an equivalence study. ' , Journal of Comparative Effectiveness Research , vol. 8 , no. 7 , pp. 523-533 . https://doi.org/10.2217/cer-2018-0108
dc.identifier.issn2042-6305
dc.identifier.otherPURE: 16689222
dc.identifier.otherPURE UUID: 5ef845f3-90a9-4dbd-abbe-8a9726b02b6c
dc.identifier.otherScopus: 85065670913
dc.identifier.urihttp://hdl.handle.net/2299/21319
dc.description© 2019 Goswami, Oliva, Ionova et al.
dc.description.abstractAim:To determine measurement equivalence of paper and electronic application of the hematologi-cal malignancy-patient-reported outcome (HM-PRO), a specific measure for the evaluation of patient-reported outcomes in HMs.Patients & methods:Following International Society of Pharmacoeconomicsand Outcomes Research ePRO Good Research Practice Task Force guidelines, a total of 193 adult patientswith different HMs were recruited into a multicenter prospective study. The paper and the electronic ver-sion of the instrument were completed in the outpatient clinics in a randomized crossover design with a30-min time interval to minimize the learning effect. Those who completed the paper version first, com-pleted the electronic version after 30 min and vice versa. Instrument version and order effects were testedon total score of the two parts of the HM-PRO (Part A: quality of life and Part B: signs & symptoms) in atwo-way ANOVA with patients as random effects. Intraclass correlation coefficients (95% CI) and Spear-man’s rank correlation coefficients were used to evaluate test–retest reliability and reproducibility. Theeffects of instrument version and order were tested on total score of the two parts of HM-PRO.Results:The questionnaire version and administration order effects were not significant at the 5% level. Therewere no interactions found between these two factors for HM-PRO (Part A [quality of life]; p=0.95); and(part B [signs and symptoms]; p=0.72]. Spearman’s rank correlation coefficients were greater than 0.9, andintraclass correlation coefficients ranged from 0.94 to 0.98; furthermore, the scores were not statisticallydifferent between the two versions, showing acceptable reliability indexes. Noteworthy, the differencebetween the completion time for both paper (mean=6:38 min) and electronic version (mean=7:29 min)was not statistically significant (n=100; p=0.11). Patients did not report any difficulty in completing theelectronic version during cognitive interviews and were able to understand and respond spontaneously.Conclusion:Measurement equivalence has been demonstrated for the paper and electronic applicationof the HM-PRO.en
dc.format.extent11
dc.language.isoeng
dc.relation.ispartofJournal of Comparative Effectiveness Research
dc.subjectHM-PRO
dc.subjecthematological malignancy
dc.subjectpaper/electronic PRO
dc.subjectHealth Policy
dc.titlePaper and electronic versions of HM-PRO, a novel patient-reported outcome measure for hematology: an equivalence study.en
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionDepartment of Clinical and Pharmaceutical Sciences
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionPublic Health and Patient Safety Unit
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85065670913&partnerID=8YFLogxK
rioxxterms.versionVoR
rioxxterms.versionofrecordhttps://doi.org/10.2217/cer-2018-0108
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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