Literature DB >> 28390550

A research note on the benefit of patient and public involvement in research: The experience of prostate cancer patients regarding information in radiotherapy.

L Gordon1, A Dickinson2, M Offredy3, J Smiddy4.   

Abstract

AIM: 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.
METHOD: 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. DISCUSSION: 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.
CONCLUSION: 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.
Copyright © 2017 The College of Radiographers. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Patient public involvement; Prostate cancer; Radiotherapy

Mesh:

Year:  2017        PMID: 28390550     DOI: 10.1016/j.radi.2017.02.004

Source DB:  PubMed          Journal:  Radiography (Lond)        ISSN: 1078-8174


  5 in total

1.  'Valued and listened to': the collective experience of patient and public involvement in a national evaluation.

Authors:  K Clare; A Ojo; J Teke; M Willis; G Akhtar; B Clegg; C Goddard; C Freeman; K J Drew; D Radley; C Homer; L Ells
Journal:  Perspect Public Health       Date:  2022-07

2.  Patient and public involvement in doctoral research: Impact, resources and recommendations.

Authors:  Nia Coupe; Amy Mathieson
Journal:  Health Expect       Date:  2019-10-15       Impact factor: 3.377

3.  Development and pre-testing of the Patient Engagement In Research Scale (PEIRS) to assess the quality of engagement from a patient perspective.

Authors:  Clayon B Hamilton; Alison M Hoens; Shanon McQuitty; Annette M McKinnon; Kelly English; Catherine L Backman; Tara Azimi; Negar Khodarahmi; Linda C Li
Journal:  PLoS One       Date:  2018-11-01       Impact factor: 3.240

4.  Patients' experience of communication and handling of symptomatic adverse events in breast cancer patients receiving adjuvant chemotherapy.

Authors:  Christina Witt Bæksted; Aase Nissen; Ann S Knoop; Helle Pappot
Journal:  Res Involv Engagem       Date:  2019-11-20

5.  Fleshing out the data: when epidemiological researchers engage with patients and carers. Learning lessons from a patient involvement activity.

Authors:  Melanie Morris; Yuki Alencar; Bernard Rachet; Richard Stephens; Michel P Coleman
Journal:  BMJ Open       Date:  2020-09-30       Impact factor: 2.692

  5 in total

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