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Journal Abstract Search

147 related items for PubMed ID: 30157687

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  • 2. Recommendations on evidence needed to support measurement equivalence between electronic and paper-based patient-reported outcome (PRO) measures: ISPOR ePRO Good Research Practices Task Force report.
    Coons SJ, Gwaltney CJ, Hays RD, Lundy JJ, Sloan JA, Revicki DA, Lenderking WR, Cella D, Basch E, ISPOR ePRO Task Force.
    Value Health; 2009 Jun; 12(4):419-29. PubMed ID: 19900250
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  • 5. Updated Recommendations on Evidence Needed to Support Measurement Comparability Among Modes of Data Collection for Patient-Reported Outcome Measures: A Good Practices Report of an ISPOR Task Force.
    O'Donohoe P, Reasner DS, Kovacs SM, Byrom B, Eremenco S, Barsdorf AI, Arnera V, Coons SJ.
    Value Health; 2023 May; 26(5):623-633. PubMed ID: 37121630
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  • 6. Capturing Patient-Reported Outcome (PRO) Data Electronically: The Past, Present, and Promise of ePRO Measurement in Clinical Trials.
    Coons SJ, Eremenco S, Lundy JJ, O'Donohoe P, O'Gorman H, Malizia W.
    Patient; 2015 Aug; 8(4):301-9. PubMed ID: 25300613
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  • 7. Equivalence of electronic and paper administration of patient-reported outcome measures: a systematic review and meta-analysis of studies conducted between 2007 and 2013.
    Muehlhausen W, Doll H, Quadri N, Fordham B, O'Donohoe P, Dogar N, Wild DJ.
    Health Qual Life Outcomes; 2015 Oct 07; 13():167. PubMed ID: 26446159
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  • 8. Does scrolling affect measurement equivalence of electronic patient-reported outcome measures (ePROM)? Results of a quantitative equivalence study.
    Shahraz S, Pham TP, Gibson M, De La Cruz M, Baara M, Karnik S, Dell C, Pease S, Nigam S, Cappelleri JC, Lipset C, Zornow P, Lee J, Byrom B.
    J Patient Rep Outcomes; 2021 Feb 27; 5(1):23. PubMed ID: 33638726
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  • 11. "Bring Your Own Device" (BYOD): The Future of Field-Based Patient-Reported Outcome Data Collection in Clinical Trials?
    Gwaltney C, Coons SJ, O'Donohoe P, O'Gorman H, Denomey M, Howry C, Ross J.
    Ther Innov Regul Sci; 2015 Nov 27; 49(6):783-791. PubMed ID: 30222388
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  • 15. Best Practices for Avoiding Paper Backup When Implementing Electronic Approaches to Patient-Reported Outcome Data Collection in Clinical Trials.
    Howry C, Elash CA, Crescioni M, Eremenco S, O'Donohoe P, Rothrock T.
    Ther Innov Regul Sci; 2019 Jul 27; 53(4):441-445. PubMed ID: 30244593
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  • 16. Diarrhea-predominant irritable bowel syndrome: creation of an electronic version of a patient-reported outcome instrument by conversion from a pen-and-paper version and evaluation of their equivalence.
    Delgado-Herrera L, Banderas B, Ojo O, Kothari R, Zeiher B.
    Patient Relat Outcome Meas; 2017 Jul 27; 8():83-95. PubMed ID: 28790875
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  • 17. PRO data collection in clinical trials using mixed modes: report of the ISPOR PRO mixed modes good research practices task force.
    Eremenco S, Coons SJ, Paty J, Coyne K, Bennett AV, McEntegart D, ISPOR PRO Mixed Modes Task Force.
    Value Health; 2014 Jul 27; 17(5):501-16. PubMed ID: 25128043
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  • 20. Validation of electronic systems to collect patient-reported outcome (PRO) data-recommendations for clinical trial teams: report of the ISPOR ePRO systems validation good research practices task force.
    Zbrozek A, Hebert J, Gogates G, Thorell R, Dell C, Molsen E, Craig G, Grice K, Kern S, Hines S.
    Value Health; 2013 Jun 27; 16(4):480-9. PubMed ID: 23796281
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