University of Hertfordshire

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Original languageEnglish
Pages (from-to)167-170
Number of pages4
Early online date27 Feb 2017
Publication statusPublished - 31 May 2017



To explore the inclusion of patient and public involvement (PPI) in a qualitative study on the experiences of men with prostate cancer regarding information in radiotherapy.

The application of PPI to one doctoral research study is explored with respect to two perspectives: firstly, involvement of a patient reference group who informed the research design and materials, and secondly, the involvement of a public involvement in research group (PIRg) in advising the researcher during the design process.

PPI is recognised as an important component of contemporary health research. PPI is becoming a common and essential requirement for high quality research projects and yet literature exploring or reporting the involvement and influence of PPI is sparse. Consideration is given to the national PPI landscape that has shaped public involvement in health research.

The contribution of PPI to this study appears to have been beneficial to the development and evaluation of the study design, the self-worth of the reference group participants and demonstrates that the value of PPI in health research should not be underestimated.


This document is the Accepted Manuscript version of the following article: L. Gordon, A. Dickinson, M. Offredy, and J. Smiddy, ‘A research note on the benefit of patient and public involvement in research: The experience of prostate cancer patients regarding information in radiotherapy’, Radiography, Vol. 23(2): 167-170, May 2017, doi: Under embargo. Embargo end date: 27 February 2018. © 2016. This manuscript version is made available under the CC-BY-NC-ND 4.0 license © 2017 The College of Radiographers. Published by Elsevier Ltd. All rights reserved.

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