2018
DOI: 10.1186/s40900-018-0129-8
|View full text |Cite
|
Sign up to set email alerts
|

Using qualitative Health Research methods to improve patient and public involvement and engagement in research

Abstract: Plain English summaryPatient engagement (or patient and public involvement) in health research is becoming a requirement for many health research funders, yet many researchers have little or no experience in engaging patients as partners as opposed to research subjects. Additionally, many patients have no experience providing input on the research design or acting as a decision-making partner on a research team. Several potential risks exist when patient engagement is done poorly, despite best intentions. Some… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

3
76
0
1

Year Published

2019
2019
2024
2024

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 87 publications
(80 citation statements)
references
References 43 publications
3
76
0
1
Order By: Relevance
“…The importance of representing of all relevant stakeholder groups including patients in COS development4 7 is increasingly recognised, as it is in wider health research 16–18. There is also growing appreciation of the importance of supporting their participation in ways that are meaningful, thus avoiding tokenism and enhancing the credibility and validity of the resulting research 19 20. However, our findings suggest that not all the interviewees thought their participation in COS development was meaningful, as the purpose and process of the study were communicated in ways that were not accessible for them.…”
Section: Discussionmentioning
confidence: 82%
“…The importance of representing of all relevant stakeholder groups including patients in COS development4 7 is increasingly recognised, as it is in wider health research 16–18. There is also growing appreciation of the importance of supporting their participation in ways that are meaningful, thus avoiding tokenism and enhancing the credibility and validity of the resulting research 19 20. However, our findings suggest that not all the interviewees thought their participation in COS development was meaningful, as the purpose and process of the study were communicated in ways that were not accessible for them.…”
Section: Discussionmentioning
confidence: 82%
“…Such qualitative inquiry should extend to patients' voices that are currently under‐researched and almost absent from the existing evidence. More dense description is required including social, demographic and health profiles of participants as well as setting and context to enhance transferability (Rolfe, Ramsden, Banner, & Graham, ). A clear representation of people with problematic substance use can give diverse perspectives to design relevant and appropriate studies and enhance sustainability (Wilson et al, ).…”
Section: Discussionmentioning
confidence: 99%
“…Further, we need to explore other study designs that could reduce burden and improve external validity such as trials embedded in registries, cohorts, or routinely collected data [43] but also observational studies and use of routinely collected data. Patient and public involvement at the planning stage of the trial could also help reduce the burden [44][45][46] and drawing on patients' experiential knowledge, ideas, and input when designing interventions to reduce research burden is essential [47][48][49][50]. The amount of data recorded as well as the modalities for recording data could also be questioned.…”
Section: Toward Minimally Disruptive and Compassionate Clinical Researchmentioning
confidence: 99%