This paper is in the following e-collections/theme issues:

Participatory Medicine & E-Patients  Clinical Information and Decision Making  Research Instruments, Questionnaires, and Tools 


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Works citing "Integrating Patient Reported Outcomes With Clinical Cancer Registry Data: A Feasibility Study of the Electronic Patient-Reported Outcomes From Cancer Survivors (ePOCS) System"

Laura Ashley, Helen Jones, James Thomas, Alex Newsham, Amy Downing, Eva Morris, Julia Brown, Galina Velikova, David Forman, Penny Wright
J Med Internet Res 2013 (Oct 25); 15(10):e230 

According to Crossref, the following articles are citing this article (DOI 10.2196/jmir.2764):

(note that this is only a small subset of citations)

 
1. Martin NE, Massey L, Stowell C, Bangma C, Briganti A, Bill-Axelson A, Blute M, Catto J, Chen RC, D’Amico AV, Feick G, Fitzpatrick JM, Frank SJ, Froehner M, Frydenberg M, Glaser A, Graefen M, Hamstra D, Kibel A, Mendenhall N, Moretti K, Ramon J, Roos I, Sandler H, Sullivan FJ, Swanson D, Tewari A, Vickers A, Wiegel T, Huland H. Defining a Standard Set of Patient-centered Outcomes for Men with Localized Prostate Cancer. European Urology 2014; [CrossRef]
 
2. Ashley L, Smith AB, Jones H, Velikova G, Wright P. Traditional and Rasch psychometric analyses of the Quality of Life in Adult Cancer Survivors (QLACS) questionnaire in shorter-term cancer survivors 15months post-diagnosis. Journal of Psychosomatic Research 2014; [CrossRef]