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Patient and public involvement in designing and conducting doctoral research: the whys and the hows
PLAIN ENGLISH SUMMARY: Evidence shows that public and patient involvement in research has a positive effect on its quality and end-results. Thus, public and patient involvement in all stages of research is becoming commonplace. There are limited detailed examples however, that describe how to make t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697942/ https://www.ncbi.nlm.nih.gov/pubmed/31428458 http://dx.doi.org/10.1186/s40900-019-0155-1 |
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author | Tomlinson, Justine Medlinskiene, Kristina Cheong, V-Lin Khan, Sarah Fylan, Beth |
author_facet | Tomlinson, Justine Medlinskiene, Kristina Cheong, V-Lin Khan, Sarah Fylan, Beth |
author_sort | Tomlinson, Justine |
collection | PubMed |
description | PLAIN ENGLISH SUMMARY: Evidence shows that public and patient involvement in research has a positive effect on its quality and end-results. Thus, public and patient involvement in all stages of research is becoming commonplace. There are limited detailed examples however, that describe how to make this possible, especially for those doing PhD research. Doctoral researchers are often new to research practice or have limited experience and are often bound by strict time and financial constraints. It is also not usually a requirement of the award to involve public and patients in their research. Hence, they may not feel confident or motivated to involve or engage with public and patients during their research. We, four doctoral researchers, share examples from our own research studies that have included different approaches to public and patient involvement. Two studies formed public and patient advisory groups who helped design the research questions, data collection tools and recruitment methods. One enlisted the help of an online public and patient panel from a local hospital. A different study worked with patients from an established group to help define key medical words. We did face some challenges, such as the need to develop good group work skills and to apply for grants to cover reimbursement, but we all found it beneficial to involve patients in our studies. We noticed a positive effect on each study’s progression and an improvement in our own self-esteem. In addition, having public and patient involvement helped reduce the isolation we felt as doctoral researchers. Thus, we strongly encourage more doctoral researchers to involve public and patients in their studies. ABSTRACT: Public and patient involvement (PPI) has been shown to have a positive impact on health and social care research. However, adequate examples describing how to operationalise effective PPI, especially in doctoral studies, are lacking. Hence, doctoral researchers new to research, or those with limited experience, can be discouraged from facilitating PPI in their research. This paper aims to describe and discuss in detail the approaches used by four doctoral researchers to incorporate PPI at different stages of their research studies from study design to disseminating findings. We aim to inform other doctoral researchers about the challenges and limitations relating to PPI that we faced. Through these, we share pragmatic recommendations for facilitating PPI during doctoral studies. The description of four case studies demonstrated that PPI could be incorporated at various stages during doctoral research. This has had a beneficial impact on our research study progression, researcher self-esteem and lastly, helped alleviate researcher isolation during doctoral studies. |
format | Online Article Text |
id | pubmed-6697942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66979422019-08-19 Patient and public involvement in designing and conducting doctoral research: the whys and the hows Tomlinson, Justine Medlinskiene, Kristina Cheong, V-Lin Khan, Sarah Fylan, Beth Res Involv Engagem Review Article PLAIN ENGLISH SUMMARY: Evidence shows that public and patient involvement in research has a positive effect on its quality and end-results. Thus, public and patient involvement in all stages of research is becoming commonplace. There are limited detailed examples however, that describe how to make this possible, especially for those doing PhD research. Doctoral researchers are often new to research practice or have limited experience and are often bound by strict time and financial constraints. It is also not usually a requirement of the award to involve public and patients in their research. Hence, they may not feel confident or motivated to involve or engage with public and patients during their research. We, four doctoral researchers, share examples from our own research studies that have included different approaches to public and patient involvement. Two studies formed public and patient advisory groups who helped design the research questions, data collection tools and recruitment methods. One enlisted the help of an online public and patient panel from a local hospital. A different study worked with patients from an established group to help define key medical words. We did face some challenges, such as the need to develop good group work skills and to apply for grants to cover reimbursement, but we all found it beneficial to involve patients in our studies. We noticed a positive effect on each study’s progression and an improvement in our own self-esteem. In addition, having public and patient involvement helped reduce the isolation we felt as doctoral researchers. Thus, we strongly encourage more doctoral researchers to involve public and patients in their studies. ABSTRACT: Public and patient involvement (PPI) has been shown to have a positive impact on health and social care research. However, adequate examples describing how to operationalise effective PPI, especially in doctoral studies, are lacking. Hence, doctoral researchers new to research, or those with limited experience, can be discouraged from facilitating PPI in their research. This paper aims to describe and discuss in detail the approaches used by four doctoral researchers to incorporate PPI at different stages of their research studies from study design to disseminating findings. We aim to inform other doctoral researchers about the challenges and limitations relating to PPI that we faced. Through these, we share pragmatic recommendations for facilitating PPI during doctoral studies. The description of four case studies demonstrated that PPI could be incorporated at various stages during doctoral research. This has had a beneficial impact on our research study progression, researcher self-esteem and lastly, helped alleviate researcher isolation during doctoral studies. BioMed Central 2019-08-16 /pmc/articles/PMC6697942/ /pubmed/31428458 http://dx.doi.org/10.1186/s40900-019-0155-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Article Tomlinson, Justine Medlinskiene, Kristina Cheong, V-Lin Khan, Sarah Fylan, Beth Patient and public involvement in designing and conducting doctoral research: the whys and the hows |
title | Patient and public involvement in designing and conducting doctoral research: the whys and the hows |
title_full | Patient and public involvement in designing and conducting doctoral research: the whys and the hows |
title_fullStr | Patient and public involvement in designing and conducting doctoral research: the whys and the hows |
title_full_unstemmed | Patient and public involvement in designing and conducting doctoral research: the whys and the hows |
title_short | Patient and public involvement in designing and conducting doctoral research: the whys and the hows |
title_sort | patient and public involvement in designing and conducting doctoral research: the whys and the hows |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697942/ https://www.ncbi.nlm.nih.gov/pubmed/31428458 http://dx.doi.org/10.1186/s40900-019-0155-1 |
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