Research for Patient Benefit Research for Patient Benefit

What does the funding stream focus on?
  • Lower cost research studies (qualitative, quantitative and mixed) to assess whether new interventions provide benefit for people with health and social care needs.

RfPB Key Information

Director: Professor Kevin Munro

Aim: To support applied health and social care research for the benefit of users of the NHS

Funding: There are 3 levels of funding (only researcher-led calls):

  • Awards of up to £500,000 over a period of up to 36 months
  • Awards for feasibility studies up to £300,000
  • Awards of up to £200,000 for higher risk projects

Process: Two-stage process (shortened application form for Stage 1) to one of the 10 regional funding panels. The process takes about 10 months.

Success rate: 50% success rate at second stage

Summary of Panel Observation Tips

  • Relatively inexperienced investigators can lead but strong mentorship must be in place
  • RfPB will not fund pilot studies (only feasibility studies)

Strengths and Weaknesses in Applications:

Strengths:

    • Strong PPI (Patient and Public Involvement) input was essential, with well-defined roles and active involvement throughout the research process.
    • Clear articulation of patient benefit and the trajectory towards achieving it, especially for interventions intended for HTA (Health Technology Assessment) trials.
    • Realistic timelines and appropriate FTE (Full-Time Equivalent) allocation for team members.
    • Strong research teams with diverse expertise and a track record of collaboration.
    • Applications targeting high-prevalence/high-burden issues or rare diseases with significant patient impact.
    • Preliminary work and evidence of team cohesion.

Weaknesses:

    • Poor PPI, including tokenistic involvement or lack of diversity in PPI groups.
    • Unrealistic timelines, lack of clarity in patient benefit trajectory, and inadequate consideration of EDI (Equality, Diversity, and Inclusion).
    • Underspecified methodologies or lack of clarity in research aims, unsuitable outcome measures, and insufficient detail on ethics.
    • Lack of originality or awareness of existing literature.
    • Concerns about the feasibility of delivering the project, including recruitment targets and intervention implementation.

Emerging Trends and Panel Preferences:

  • The panel actively sought to fund ECRs (Early Career Researchers) but emphasized the need for suitable support.
  • There was an increasing emphasis on implementation, dissemination, and next steps in research.
  • The panel supported new and innovative approaches but required a thorough consideration of risks and mitigation strategies.
  • EDI considerations were crucial, with panels attuned to vague or inadequate EDI plans.
  • The panel acknowledged the importance of methodological research and welcomed applications from under-represented disciplines.
  • Regional prevalence: The panel will now consider the relevance of the topic based on regional prevalence, suggesting that research addressing health issues prevalent in the specific region may be prioritised.
  • Committee's support for revisions: The committee was supportive and tried to invite as many Stage 1 applications as possible to Stage 2, suggesting a willingness to provide feedback and encourage revisions.
  • Detailed examples of feedback: The observations provide specific examples of the feedback given to applicants, including minor and major fixable faults, and reasons for not funding applications.

Summary of feedback

across 12 outcome letters - RDS database from 1 June 2022

Common themes
  1. Rationale and justification:
    • Many proposals lacked a clear rationale or justification for the need for the research.
    • Proposals often failed to adequately demonstrate the added value of their research in the context of existing knowledge, guidelines, or similar studies.
  2. Methodology:
    • Methodological issues were frequently cited, including insufficient detail and clarity.
    • Specific concerns included:
      • Feasibility of timelines and budgets.
      • Justification of sample sizes and intervention time points.
      • Lack of robust evaluation
  3. Patient and Public Involvement:
    • Most proposals were criticized for under-developed PPI plans, insufficient representation, or lack of clarity on the role of PPI representatives.
    • Proposals were encouraged to engage diverse and appropriate groups, including children, young people, and carers.
  4. Recruitment and Inclusion:
    • Recruitment strategies and inclusion criteria were questioned for feasibility and equity.
    • Concerns about potential biases in participant selection and representation were noted.
  5. Plain English Summaries:
    • Several proposals were asked to rewrite their PES to eliminate jargon and ensure accessibility to non-specialist audiences.
Key takeaways for future applications
  • Strengthen Rationale: Clearly articulate the need for the research and its added value compared to existing knowledge and practices.
  • Enhance Methodological Detail: Provide robust, detailed methodologies, including feasibility studies, safety assurances, and recruitment plans.
  • Improve PPI Engagement: Expand and diversify PPI representation and clarify their roles throughout the research.
  • Simplify PES: Ensure plain English summaries are free of jargon and accessible to lay audiences.
  • Address Feasibility Concerns: Realistically align project goals, timelines, and budgets to ensure deliverability.
Application-specific highlights

1: Criticized for insufficient articulation of research value and under-developed PPI.

2: Raised concerns about methodological gaps, feasibility, and health economic evaluation.

3: Highlighted strong co-production but raised concerns about unclear social care trajectory and potential biases in recruitment.

4: Identified issues with justification, online meeting inclusion, and inadequately described outcomes and timelines.

5: Emphasized unclear study rationale and under-developed PPI.

6: Highlighted insufficient methodological detail and lack of a statistician on the team.

7: Noted concerns with self-medication risks, withdrawal protocols, and unclear NHS integration.

8: Questioned the added value, subpopulation analysis, and limited PPI involvement.

9: Identified unrealistic aims and recruitment challenges.

10: Requested clarity on feasibility, methodology, and mitigation of NHS delays.

11: Requested refinements to methodology, including clarity on instrument design and systematic review.

12: Praised for EDI focus but criticized for unclear study rationale and insufficient time commitment from team members.

Funding Deadlines

Call Webinar Outline submission deadline Outcome date Full submission deadline Outcome date

RfPB

  9 July 25 October 25 November 25 March 26

RfPB Under-represented disciplines and specialisms highlight notice: Other Registered Health and Care Professionals

  9 April July 25 Oct 25 Feb 26

RfPB - Comp 56

  5 March 25 June 25 July 25 Nov 25

RfPB - Comp 55

  6 Nov 24 Feb 25 March 25 July 25

RfPB - Comp 54

  July 24 Oct 24 Nov 24 March 25

RfPB Example

Enhancing the efficacy of non-invasive ventilation for patients with motor neurone disease: synthesising the evidence, mapping the services and translating the evidence into clinical practice

Funding: £217k, 2018-2020

Aim: To identify the best ways to provide non-invasive ventilation services to people with motor neurone disease and to use this information to develop resources to ensure patients get the best service possible.

Other RfPB Examples

  • Co-production of best practice recommendations for local authority reviews of double-handed homecare packages
  • WISE (Wrist Injury Strengthening Exercise): a randomised multicentre feasibility study of resistance exercise versus usual care for optimising function after distal radius fracture in adults aged 50 years or over
  • Preventing psychosis in young people at ultra-high-risk attending NHS mental health services: a feasibility study of a novel intervention target
  • Quantifying and implementing patient preferences for the treatment of high-risk rectal cancer, including the new strategy of organ preservation: PrefCoRe project