Literature DB >> 16192583

Communicating quality of life information to cancer patients: a study of six presentation formats.

M Brundage1, D Feldman-Stewart, A Leis, A Bezjak, L Degner, K Velji, L Zetes-Zanatta, D Tu, P Ritvo, J Pater.   

Abstract

PURPOSE: To determine which formats for presenting health-related quality of life (HRQL) data are interpreted most accurately and are most preferred by cancer patients. Patients often want a great deal of information about cancer treatments, including information relevant to HRQL. Clinical trials provide methodologically sound HRQL data that may be useful to patients. PATIENTS AND METHODS: In a multicenter study, 198 patients with previously treated cancer participated in a structured interview. Participants judged HRQL information presented in one textual and five graphical formats. Outcome measures included the accuracy of patients' interpretations and ease-of-use and helpfulness ratings for each format.
RESULTS: Correct interpretations ranged from 85% to 98% across formats (F = 10.3, P < .0001) with line graphs of mean HRQL scores over time being interpreted correctly most often. Older patients and less-educated patients were less likely to interpret graphs accurately (F = 7.3, P = .008; and F = 10.6, P = .001, respectively), but all groups were most accurate on simple line graphs. Multivariate analysis revealed that format type, participant age and education were independent predictors of accuracy rates. Patients' ratings also varied across formats both for ease of understanding scores (F = 12.1, P < .0001) and for helpfulness scores (F = 13.2, P < .0001), with line graphs being rated highest on both outcomes.
CONCLUSION: Patients generally prefer a simple linear representation of group mean HRQL scores, and can accurately interpret data presented in this format more than 98% of the time irrespective of their age group and educational level. The findings have important implications for the communication of clinical trial HRQL results.

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Year:  2005        PMID: 16192583     DOI: 10.1200/JCO.2005.12.514

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  40 in total

1.  Democratising and vitalising family practice by patient-centred medicine.

Authors:  Hakan Yaman; Melahat Akdeniz; Hasan Hüseyin Avci; Jürgen Howe
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Review 2.  Patterns of reporting health-related quality of life outcomes in randomized clinical trials: implications for clinicians and quality of life researchers.

Authors:  Michael Brundage; Brenda Bass; Judith Davidson; John Queenan; Andrea Bezjak; Jolie Ringash; Anna Wilkinson; Deb Feldman-Stewart
Journal:  Qual Life Res       Date:  2010-11-26       Impact factor: 4.147

Review 3.  [The benefits of using patient-reported outcomes in cancer treatment: an overview].

Authors:  Lisa M Wintner; Johannes M Giesinger; Georg Kemmler; Monika Sztankay; Anne Oberguggenberger; Eva-Maria Gamper; Barbara Sperner-Unterweger; Bernhard Holzner
Journal:  Wien Klin Wochenschr       Date:  2012-04-27       Impact factor: 1.704

Review 4.  Quality of life after surgery for colorectal cancer: clinical implications of results from randomised trials.

Authors:  Sameer Gujral; Kerry N L Avery; Jane M Blazeby
Journal:  Support Care Cancer       Date:  2007-11-20       Impact factor: 3.603

5.  Issues in the design of Internet-based systems for collecting patient-reported outcomes.

Authors:  James B Jones; Claire F Snyder; Albert W Wu
Journal:  Qual Life Res       Date:  2007-08-01       Impact factor: 4.147

6.  Design and evaluation of a web-based interactive visualization system for lung transplant home monitoring data.

Authors:  David S Pieczkiewicz; Stanley M Finkelstein; Marshall I Hertz
Journal:  AMIA Annu Symp Proc       Date:  2007-10-11

7.  Quality-of-life outcomes for adjuvant chemotherapy in early-stage non-small-cell lung cancer: results from a randomized trial, JBR.10.

Authors:  Andrea Bezjak; Christopher W Lee; Keyue Ding; Michael Brundage; Timothy Winton; Barbara Graham; Marlo Whitehead; David H Johnson; Robert B Livingston; Lesley Seymour; Frances A Shepherd
Journal:  J Clin Oncol       Date:  2008-09-22       Impact factor: 44.544

8.  A knowledge translation challenge: clinical use of quality of life data from cancer clinical trials.

Authors:  Michael Brundage; Brenda Bass; Ringash Jolie; Kimberley Foley
Journal:  Qual Life Res       Date:  2011-01-29       Impact factor: 4.147

9.  The effect of format on parents' understanding of the risks and benefits of clinical research: a comparison between text, tables, and graphics.

Authors:  Alan R Tait; Terri Voepel-Lewis; Brian J Zikmund-Fisher; Angela Fagerlin
Journal:  J Health Commun       Date:  2010-07

10.  Using informatics to capture older adults' wellness.

Authors:  George Demiris; Hilaire J Thompson; Blaine Reeder; Katarzyna Wilamowska; Oleg Zaslavsky
Journal:  Int J Med Inform       Date:  2011-04-08       Impact factor: 4.046

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