Literature DB >> 24766686

Can electronic web-based technology improve quality of life data collection? Analysis of Radiation Therapy Oncology Group 0828.

Benjamin Movsas1, Daniel Hunt2, Deborah Watkins-Bruner3, W Robert Lee4, Heather Tharpe5, Desiree Goldstein6, Joan Moore7, Ian S Dayes8, Sara Parise9, Howard Sandler10.   

Abstract

PURPOSE: Missing data are a significant problem in clinical trials, particularly for quality of life (QOL), which cannot be obtained retrospectively. The purpose of this study was to evaluate the feasibility of an electronic web-based strategy for QOL data collection in a cooperative group radiation oncology trial setting. METHODS AND MATERIALS: Radiation Therapy Oncology Group (RTOG) 0828 was a prospective National Cancer Institute cooperative group companion study of RTOG-0415, a randomized study of conventional versus hypofractionated radiation. Forty-nine English-speaking patients with favorable risk prostate cancer who enrolled on RTOG-0415 consented to using web-based technology for completing QOL. In RTOG-0415, using paper forms, the 6-month QOL compliance rate was 52%. The purpose of RTOG-0828 was to test the feasibility of a web-based strategy with the goal of increasing the 6-month QOL completion rate by 25% (from 52% to 77%) for a relative improvement of ~50%. The web-based tool used in this study was VisionTree Optimal Care (VTOC; VisionTree Software, Inc, San Diego, CA), a Health-Insurance-Portability-Accountability-Act secure, online technology that allows real-time tracking and e-mail reminders. The primary endpoint was the 6-month compliance rate for the validated QOL instrument, Expanded Prostate Index Composite.
RESULTS: The QOL completion rate at baseline was 98%. Compared with the prior 52% QOL completion rate at 6 months using paper forms, the QOL web-based completion rate at 6 months was 90% (2-sided P value < .001). At 12 months, the EPIC completion rate was 82% (compared with 36% using paper forms).
CONCLUSIONS: This RTOG study suggests that a web-based strategy to collect QOL appears to be feasible in the cooperative group radiation oncology trial setting and is associated with an increase in the 6-month QOL compliance rate compared with the prior method of using paper forms. The RTOG plans to further test this strategy in a head-and-neck cancer trial across all participating RTOG sites.
© 2014. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 24766686      PMCID: PMC4007315          DOI: 10.1016/j.prro.2013.07.014

Source DB:  PubMed          Journal:  Pract Radiat Oncol        ISSN: 1879-8500


  11 in total

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Journal:  Onkologie       Date:  2011-08-19

2.  Implementing musculoskeletal outcome assessments in clinical practice.

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Journal:  Haemophilia       Date:  2012-07       Impact factor: 4.287

3.  Learning to live with missing quality-of-life data in advanced-stage disease trials.

Authors:  Gary W Donaldson; Carol M Moinpour
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Review 4.  Statistical analysis of quality of life with missing data in cancer clinical trials.

Authors:  A B Troxel; D L Fairclough; D Curran; E A Hahn
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Review 5.  Electronic patient-reported outcome systems in oncology clinical practice.

Authors:  Antonia V Bennett; Roxanne E Jensen; Ethan Basch
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6.  The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005-2008.

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7.  Towards the Implementation of Quality of Life Monitoring in Daily Clinical Routine: Methodological Issues and Clinical Implication.

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9.  Equivalence of electronic and paper-and-pencil administration of patient-reported outcome measures: a meta-analytic review.

Authors:  Chad J Gwaltney; Alan L Shields; Saul Shiffman
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10.  Investigating the missing data mechanism in quality of life outcomes: a comparison of approaches.

Authors:  Shona Fielding; Peter M Fayers; Craig R Ramsay
Journal:  Health Qual Life Outcomes       Date:  2009-06-22       Impact factor: 3.186

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Authors:  Jeffrey M Vainshtein; Dominic H Moon; Felix Y Feng; Douglas B Chepeha; Avraham Eisbruch; Matthew H Stenmark
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4.  The Complementary Nature of Patient-Reported Outcomes and Adverse Event Reporting in Cooperative Group Oncology Clinical Trials: A Pooled Analysis (NCCTG N0591).

Authors:  Pamela J Atherton; Deborah W Watkins-Bruner; Carolyn Gotay; Carol M Moinpour; Daniel V Satele; Kathryn A Winter; Paul L Schaefer; Benjamin Movsas; Jeff A Sloan
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Review 5.  Patient-reported outcomes and survivorship in radiation oncology: overcoming the cons.

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6.  Quality of Life Analysis of a Radiation Dose-Escalation Study of Patients With Non-Small-Cell Lung Cancer: A Secondary Analysis of the Radiation Therapy Oncology Group 0617 Randomized Clinical Trial.

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7.  Methods for Implementing and Reporting Patient-reported Outcome (PRO) Measures of Symptomatic Adverse Events in Cancer Clinical Trials.

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8.  Stereotactic Body Radiation Therapy for Prostate Cancer: What is the Appropriate Patient-Reported Outcome for Clinical Trial Design?

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9.  Clinical Outcome Assessments Toolbox for Radiopharmaceuticals.

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10.  eRAPID electronic patient self-Reporting of Adverse-events: Patient Information and aDvice: a pilot study protocol in pelvic radiotherapy.

Authors:  Patricia Holch; Simon Pini; Ann M Henry; Susan Davidson; Jacki Routledge; Julia Brown; Kate Absolom; Alexandra Gilbert; Kevin Franks; Claire Hulme; Carolyn Morris; Galina Velikova
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