Public engagement with research
Public engagement, involvement and research dissemination are embedded in the work we do.
Applied health research is at the forefront of making a difference to people's lives. In the Nuffield Department of Primary Care Health Sciences, discussing our research with the public, and listening to their views, is supported and encouraged because it:
- nurtures a society where researchers and the public can develop shared ownership over the direction of health research,
- empowers citizens to make more informed lifestyle choices, question the evidence base of research and become more involved in the research process,
- enriches the professional development of our researchers, allowing them to become better communicators and gain deeper insights into how their research can benefit the lives of others,
- helps to advance health policy, so new developments can be implemented quickly for patient benefit.
- involves the public and ultimately makes our research better.
HOW WE SUPPORT RESEARCHERS
As well as coordinating communications and public events centrally and in partnership with other organisations, we provide support and guidance to researchers through our own in-house team and other public engagement and communications staff across the Medical Sciences Division and the wider University. This includes:
- support to develop research dissemination and public engagement plans in grant applications,
- opportunities to get involved in University-led and other local and national public engagement initiatives,
- a department research blog
- Patient and Public Involvement (PPI) activities, supported by a departmental PPI strategy
- training for researchers in public engagement, media skills and writing skills,
- support for media outreach working closely with the University of Oxford Media Relations Team,
- an in-house team of communications and public engagement professionals either providing support across the department or acting as communications/PPI/engagement leads on externally-funded programmes.
Helpful links:
"Our vision is to embed high-quality and innovative public engagement as an integral part of research culture and practice at Oxford, enhancing our position as a world-leading research institution."
Public Engagement with Research Strategic Plan, University of Oxford.
Contacts:
-
Gavin Hubbard
Communications and Public Engagement Officer
-
Polly Kerr
NIHR Oxford BRC PPI Manager
-
Dan Richards-Doran
Head of Communications
Latest news:
Public engagement and involvement proposals given green light
16 July 2019
The projects will reach out to rural communities and black and ethnic minority groups - audiences who are seldom engaged in primary care research.
Blog posts
Setting the research agenda in advanced heart failure
7 July 2020 | 1 comment
Dr Nick Jones, Wellcome Trust Doctoral Research Fellow, writes about the Research Priorities in Advanced Heart Failure project, which has now published its top 10 priorities for the research community.
British South Asian patients’ views on text messages to support type 2 diabetes
The number of people with type 2 diabetes is increasing globally, a condition that disproportionately affects South Asians. Text messages to support people to manage their diabetes show promise. They are cheap, accessible, and can positively impact blood sugar levels. Senior Qualitative Researcher Dr Suman Prinjha writes about her research (published in JMIR mHealth and uHealth) on how a text messaging system could support medication use in British South Asian people with diabetes.
Meat your persona: talking to Oxford's shoppers
9 August 2019
The LEAP team have been talking to shoppers to learn more about their meat and dairy consumption and to share the results of their research into the environmental and health impacts with the public.
Scientific and lay authors: writing together
18 July 2018
Lynne Maddocks, NDPCHS and NIHR CLAHRC PPI Co-ordinator, interviews one of the lead authors and lay co-authors of the recently published scientifc paper. The paper argues for a re-think in how doctors talk to their patients about kidney health, suggesting it should be about ‘kidney age’ not ‘kidney disease.’