Our research thrives on public involvement. We value the insights of our PPI members, treating them as integral to our work. We involve members of the public throughout the research process and in the management of our programme, ensuring their opinions are heard, taken into account, and acted upon. What is PPI? Patient and public involvement (PPI) is when members of the public are actively involved in academic research. In clinical, health and social care research, this includes: Patients Potential patients Carers People who use health and social care services The “general public” PPI is different from public engagement. Public engagement is when information, results or knowledge from or about a research project is shared with the public. PPI is when patient and public members contribute to how the research is designed, conducted, interpreted, and communicated. Useful links Here are a few useful links to find out more about PPI more generally in the UK: NIHR: Be part of research HDR UK: Involving and engaging patients and the public What does PPI mean to us? At Inflammation and Immunity, we recognise that effective PPI is essential for producing high quality research that is relevant and benefits the people it impacts. Our PPI members provide us with expertise and insight that is equally as valuable as the academic and clinical members of our team. Drawing upon their real-life experiences, they challenge us to think beyond the scope of our research. For example: The broader implications of our work How we design and conduct our research How we access, link, store, secure and use sensitive patient data How we can build public trust How we communicate and engage beyond academia and clinical settings How is PPI embedded throughout our programme? Our PPI Team PPI is one of our programme’s cross-cutting themes that extends across our portfolio of work. We have a centrally funded PPI Team. This team consists of: Dr Tracy Jackson, Senior Research Fellow and PPI Lead Ms Karen Mooney, PPI Lay Lead Ms Anna Grosse, PPI Lay Lead Tracy, Karen and Anna are active members of our steering group, ensuring that a culture of listening to and acting upon public voices starts from the top down. Dr Tracy Jackson: Patient and Public Involvement Lead I will work together with patients and members of the public to support the driver programme to produce research that matters. Image Tracy Jackson, PPI Lead Programme Theme(s): PPI & Communications Dr Tracy Jackson is Inflammation and Immunity’s Patient & Public Involvement (PPI) Lead, tasked with creating and implementing our PPI strategy. She is supported by our Research Administrator, Lily Quinlan. Dedicated and highly experienced, Tracy’s comprehensive approach to PPI will help ensure that projects within our programme produce high-quality, impactful research that is relevant to the people it is meant to benefit. To do this, Tracy will identify and facilitate opportunities for the patient, public and community members to share their insights and be meaningfully involved across all areas of our programme. This includes collaborating with our two Lay Leads – Anna Grosse and Karen Mooney – in attending all steering group (senior management) meetings, ensuring that a culture of listening to, and acting upon, public voices begins from the top-down. Tracy will also coordinate with existing PPI groups and networks to run a range of activities that will shape our research, as well as engage with a wider audience to highlight the work being carried out. Read Tracy's professional profile Ms Karen Mooney: Patient and Public Involvement Lay Lead “I see PPIE as the touchstone within health data research to ensure and secure the integrity of purpose, process and public engagement.” Image Karen Mooney, PPI Lay Lead Programme Theme(s): PPI & Communications Karen Mooney is a member of our Steering Group and one of our Lay Leads whose public voice will help shape our programme. Her experience with Crohn’s disease fuels her interest in chronic inflammatory conditions and their impact on overall health and well-being. She wants to see how the programme can help improve patient care and outcomes. Passionate and inquisitive, Karen challenges our team to think about the broader implications of our research, how we talk about our findings and how we engage with patients and the public to develop a collaborative approach to future research. A qualified Human Resources professional, Karen retired from Local Government due to ill health. She has since delivered health awareness training in areas of deprivation and has served as a Lay Chair of the Patients Group of the RCGPNI. Previous Patient and Public Involvement (PPI) participation includes projects such as CO-CONNECT, GRAIMATTER & COALESCE, and co-chairing a workshop at the first Advance Pain Discovery Platform (APDP) conference. Aside from her interest in health, a growing involvement in the Arts led Karen to host community radio and television programmes and publish her poetry with The Hedgehog Poetry Press. Relevant links Find out more about APDP Find out more about COALESCE Find out more about CO-CONNECT Find out more about GRAIMATTER Visit The Hedgehog Poetry Press Miss Anna Grosse: PPI Lay Lead I hope that the Inflammation and Immunity Driver Programme can lay the foundation for an inclusive and combined approach towards future research between members of the public, patients, academics & researchers. Image Anna Grosse, PPI Lay Lead Programme Theme(s): Patient & Public Involvement Miss Anna Grosse is one of Inflammation and Immunity’s PPI Lay Leads. She works with Dr Tracy Jackson and Karen Mooney to ensure that patient and public voices are meaningfully integrated across our research portfolio and embedded within our research culture. As a person living with asthma, Anna provides our programme with invaluable insight based on her lived experience. Anna’s perspective on what it is like to manage and receive treatment for a chronic inflammation-mediated condition will help in shaping our research aims, methods, approaches to external engagement and dissemination. Curious by nature, Anna is eager to know more about research related to respiratory disorders. She is also very keen to explore and learn more about the emotional, physical, psychological and social aspects of living with a chronic condition. Prior to joining our programme, Anna was a Children and Young People (CYP) PPI member with the Asthma UK Centre for Applied Research, an experience she found both interesting and enjoyable. She hopes that her experiences and knowledge gained from both her previous and ongoing PPI projects will allow her to assist with, and be of benefit to, future research. She is currently studying Psychology at Heriot-Watt University in Edinburgh. A diverse range of activities Our PPI Team is dedicated to planning, coordinating, and delivering meaningful PPI activities throughout the programme’s lifecycle, ensuring that patient and public perspectives are included at all stages. This will include: Ensuring representation and active participation in our steering group meetings Supporting our research groups in developing projects that are relevant and beneficial to members of the public Connecting and developing relationships with other PPI and community groups to ensure a range of perspectives are heard Assisting in the understanding of outcomes. Contributing to academic / research papers as co-authors Supporting specific communications activities, such as contributing to plain English summaries and creating infographics Regular evaluation of our programme’s PPI efforts to ensure continuous improvement Compensation We compensate PPI members for their contributions to our PPI activities following NIHR guidelines. Find out more about the NIHN’s guidance for PPI payments Any questions? If you have any questions about our PPI activities, please contact our PPI Lead, Dr Tracy Jackson. Email Tracy Jackson Page publication date: 9/11/2023 Last updated: 28/03/2024 This article was published on 2024-09-24