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Enhancing Patient & Public Involvement in Research: Supporting Researchers Working with Public & Patient Groups

This session provides an introduction to patient and public involvement in research, showcasing the benefits and examples of PPI in healthcare. It also highlights the historical lack of involvement and tokenism, emphasizing the need for meaningful collaboration. Learn from the experience of the Improving Patient Safety Project and explore the development of user-informed approaches to improving patient safety.

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Enhancing Patient & Public Involvement in Research: Supporting Researchers Working with Public & Patient Groups

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  1. Patient & Public Involvement in researchSupport for Researchers Working with Public & Patient Groups Susan Hrisos, Senior Research Associate & Dave Green, PPI representative May 2014

  2. Format of session • Introduction to Patient & Public Involvement in Research • Experience of ‘doing’ PPI • Researcher • PPI representative • Interactive session • Small group work

  3. Patient & Public Involvement (PPI) • Huge increase in the involvement of patients in improving their health & healthcare in recent decades • Examples: shared decision making; self-management of chronic illness; development of healthcare policy, clinical guidelines & patient literature • Evidence of benefit from involvement in healthcare: • active participation during consultations is associated with better health outcomes (Kaplan 1989; Kaplan 1996) • increased involvement improves aspects of medical care (Atkin 1998; Liaw 1996) • involvement improves treatment compliance (Bibowski 2001)

  4. PPI in improving Research • Historically patients & public have not had a large influence on research prioritisationor commissioning, and have not been involved in the research process • Research can seem irrelevant to patient & public needs • Dissemination of findings to take too long

  5. Patient & Public Involvement in Research • PPI has become an important part of research activity & is supported by government & health policy • NHS Research Governance Framework (2010): patients should be “active partners” in the research process • INVOLVE: Unique national advisory group that promotes patient & public involvement in research, supported by NIHR Central Commissioning Facility. (INVOLVE www.invo.org.uk) • Expectation of PPI contribution that goes beyond “tokenism” I.e. To have a more meaningful & identifiable role, e.g. advising on research proposals; assisting in project design Tokenism Is OUT!

  6. INVOLVE • Unique national advisory group that promotes consumer involvement in research • Supported by NIHR Central Commissioning Facility • “Involvement” = an active partnership between public & researchers in the research process rather than the use of people as research “subjects”. (INVOLVE definition. www.invo.org.uk) • rationale for PPI is the production of research that will • be more relevant to people & more likely to be used • reflect the needs & views of the public • be more likely to produce results that can be used to improve practice and social care • Promotes involvement in all aspects of the research process, including • Design of questionnaires & topic guides • Preparing patient information • Conducting interviews & focus groups • Analysing transcripts

  7. Learning from experience

  8. From novice to expert in 3.5 years.  PPI, research and learning curvesReflections from the “Improving Patient Safety Project” Susan Hrisos Senior Research Associate Dave Green Patient Participant & PPI research team member This is independent research funded by the NIHR under its Programme Grants for Applied Research scheme (RP-PG-0108-10049). The views expressed in this presentation are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health.

  9. NIHR Patient Safety Programme: “Improving patient safety through the involvement of patients” (Programme Lead: Prof. John Wright. Academic Lead: Prof Ian Watt) • Project 2: Bradford • Patient error reporting system • Lead: Prof.Gerry Armitage • Project 1: Bradford • Patient measure of organisational safety • Lead: Prof.Rebecca Lawton • Project 3: Leeds • Patient-centred training programme • Lead: Prof Vikram Jha • Project 4: Newcastle • Direct patient intervention to reduce their risk of harm • Lead: Prof. Richard Thomson Core focus: Development of user-informed approaches to improving patient safety.

  10. Annual Steering Seminar 2010 Programme research Day Research stream within PS Conference 2013 Scrutiny committee Patient Panel meeting 6 monthly 3monthly informal meetings Website & email fora Newsletter Scientific Steering YQSR group meeting 3 monthly Panel Chairs Progress meeting 3 monthly Project 1 team meeting 2 monthly PPI ‘pre-team meeting’ meeting Ad Hoc interim PPI meetings ‘Business ‘emails ‘Maintenance’ emails Dissemination activities Project 4 team meeting 2 monthly Programme PPI: Steering Structure Project 4 team meeting 2 monthly Project 4 team meeting 2 monthly

  11. Newcastle Project: Co-design

  12. Newcastle Project: ‘Extra-curricular’ PPI • Assistance with patient recruitment for interview • Participant observation in a patient focus group • Analysis of focus group transcript • Co-facilitated a creative thinking workshop with PPI peers • Development & design of ThinkSAFEintervention materials • Local & national dissemination of study & developments • Piloted patient focussed materials & data collection measures

  13. Interactive Session Involvement Research

  14. Small group exercise Your seedling research idea is awaiting “involvement nitrate” • Task One (10 mins): • As a group … • Discuss your research projects. • Identify who might be your key stakeholders. • Think about … • Who do you need to involve & when? • Where are they in the bigger picture? • Why are they important? • Place your stakeholders on the diagram

  15. Small group exercise #1 • Task Two (5- 10mins): • Imagine that you already have a “Dave” • on your research team … • What might his role be in enhancing stakeholder engagement & involvement in your research? • How can he help feed your research with their perspective ? • What research activities might he contribute to? • Place “Dave” on your diagram where you think • he has a role to play. • Write down what this role isat this place. Task Three (5mins per group): Feedback on one aspect of “Dave’s” potential PPI contribution

  16. Research Cycle INVOLVEhttp://www.invo.org.uk/posttyperesource/where-and-how-to-involve-in-the-research-cycle/

  17. Task 2 In small groups discuss: • What might involvement look like at the different stages of the research cycle? • How have/would you go about involving people? • Who have/would you involve? • Why involve - what impacts do you anticipate? Prepare feedback on: • Proposed PPI involvement at different stages • Anticipated impact relative to proposed involvement Feedback to full group (2-3mins)

  18. Thank you!

  19. Some challenges … Patient Panel • Group dynamics & cohesion - variation in commitment • Communication between members between meetings • Expectations &clarity of PPI role • PPI understanding of research process & methods Researchers • Inter-personal dynamics – managing relationships • Communication between meetings • Balancing PPI preferences for level or type of involvement • Managing expectations & having clarity of PPI role • Concerns about undermining research quality & rigour • Additional work load/demands on time

  20. Some solutions … Clarity of roles, expectations: • Terms of reference for PP & researchers • PPI Mentor PP Training: • Research process • Research methodologies Facilitating communication: • PP newsletter; PP website forum, PP email forum • Informal ‘coffee morning’ meetings • Increased contacts with researchers Accepting that we might not always get it right

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