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Exploring the value of research through the eyes of researchers and the public Understanding the relative valuation of research impact: A best-worst scaling experiment of the general public and biomedical and health researchers Policy briefing August 2016

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Page 1: Exploring the value of research through the eyes of

Exploring the value of research through the eyes of researchers and the publicUnderstanding the relative valuation of research impact: A best-worst scaling experiment of the general public and biomedical and health researchers

Policy briefingAugust 2016

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Why is a better understanding of the value of different research impacts needed?

There is increasing evidence and recognition that UK research has a positive impact on society and the economy.1-4 In the sphere of biomedical and health research, successfully demonstrating impact can make or break a grant application.

Research funders are increasingly interested in measuring the societal and economic contributions of research. For example, the 2014 Research Excellence Framework (REF) included the review and grading of 6,975 impact case studies by researchers and research users. The results of the REF are used to allocate around £1.6 billion to higher education research institutes every year.5 With 20 per cent of funding being allocated on the basis of impact, there is a clear need for robust, fair and transparent assessments.

Yet, do we have a sound empirical understanding of which of the many potential impacts of biomedical and health research are most valued by its beneficiaries (the public) and producers of research?

This Medical Research Council (MRC)-funded study by Pollitt and colleagues provides new insights into the value of biomedical and health research impacts though the eyes of two significant stakeholder groups: the public and researchers.6 It is the first study to use best-worst scaling (BWS) to measure the types of research impact that most matter to people.

BWS survey responses from 899 researchers and 1,000 members of the public were used to develop a model comparing the preferences of the two groups. The investigators uncovered notable differences in the way that the public and researchers prioritise research impacts. Although further refinement and replication is needed, they also demonstrated the utility of the BWS model for quantitative assessment and valuation of research impact.

‘The valuation of research impact currently rests on weak empiric foundations. This in turn raises questions about the reliability of impact assessment and whether current processes are robust, fair and transparent. Our research is a first step in understanding how research impacts are assessed and valued by different stakeholders.’

Professor Jonathan GrantDirector of the Policy Institute at King’s

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How were opinions on the value of different research impacts collected and analysed?

The investigators used a BWS method to understand the value that members of the public and MRC-funded researchers gave to different research impacts.

• The content and structure of the two surveys were developed based on a literature search, and refined and tested through focus groups, interviews and a pilot (see figure 1).

• The different themes (or domains) of impact tested in the surveys focussed on furthering knowledge, international/national recognition, training opportunities, creation of jobs, private sector investment, improving life expectancy, cost-efficiency and quality of care, and dissemination and consulting. For each domain, four statements regarding the impact of research were drafted.

• Both public and researcher surveys were based on eight tasks. For each task, responders were asked to choose which statement regarding impact in a list of eight was the ‘most important’, ‘second most important’, ‘least important’ and ‘second least important’.

• Members of the public were recruited online through ResearchNow, while MRC-funded researchers were recruited via email invitation.6 In total, 1,171 researchers and a representative sample of 1,000 members of the public fully or partially completed the surveys between February and March 2015, although 272 responses from the public were excluded following quality control.a

• For comparison purposes, the relative value placed on each research impact (by respondent group) was converted into a common unit, using the value placed on ‘an additional year of life expectancy for 10 per cent of adults living with a common chronic disease in the UK’ as the comparator.

a 272 responders judged to be less reliable were excluded from the model based on a fast completion time (<5 mins), lack of understanding of the choice task, or an inability to make choices within tasks.

Figure 1: Survey development process

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Which impacts of research are most valued by the public and researchers?

For the first time, the use of BWS to quantify and compare research impacts has been demonstrated. The public and researchers alike considered one of the highest priorities to be increasing life expectancy for adults living with a common chronic disease. Both groups also prioritised impacts related to the cost or quality of care and creating jobs across the UK.

Additional key findings were:

• Both the public and researchers least valued impacts centred around dissemination (public lectures, school talks and media interviews).

• Of the 28 different impacts included in the model, there was a significant difference in the value that the general public placed on 20, compared with researchers.

• Although both groups were concerned about the cost of care, this was a particularly high priority for the public.

• When it comes to training, the public placed a higher priority on the training of medical professionals than academics, while researchers had the opposite preference.

• Researchers placed a higher value on commercial impacts that attract foreign investment than those that encourage new commercial investment in research studies or facilities, while the public saw equal value in all four commercial impact statements.

Figure 2: Preferences for different types of research impact, expressed in terms of ‘additional years of life expectancy (AYLE) for 10 per cent of adults living with a common chronic disease in the UK’. Solid bars indicate impacts that are statistically different between the general public and researchers (p<0.05).ba

b The value placed on improved life expectancy is not shown as it has been used to allow comparison of researcher and public views.

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‘The general public and researchers may value research impact differently. In our study, there was a statistically significant difference in the value that these two stakeholder groups placed on 20 out of 28 impacts.’

Alexandra Pollitt Research Fellow, the Policy Institute at King’s

What next? Towards better alignment of research with public priorities

Better understanding of the value of different research impacts is crucial to ensuring that decisions regarding research funding are fair, consistent and reflect the priorities of the taxpayer, as funder.

Pollitt and colleagues have shown how the BWS methodology can be used to quantify preferences regarding research impacts, as well as how these preferences can be compared across discrete groups.

While the research is a first step in understanding how research impacts are assessed and valued, it indicates the potential of this modelling for the future development of useful metrics. With further research to validate and improve the modelling, it may be possible to develop metrics that capture different stakeholder valuations of research, which could be used for both assessment and allocation purposes. This is a longer term objective and should not be advocated based on the current study.

References1. Health Economics Research Group, Office of Health Economics, RAND Europe, Medical Research: What’s it

Worth? Estimating the economic benefits from medical research in the UK, 2008, London, UK: UK Evaluation Forum, http://www.wellcome.ac.uk/stellent/groups/corporatesite/@sitestudioobjects/documents/web_document/wtx052110.pdf (accessed October 2015).

2. Glover M, Buxton M, Guthrie S, et al., ‘Estimating the returns to UK publicly funded cancer-related research in terms of the net value of improved health outcomes’, BMC Medicine, 2014; 12:99 (doi:10.1186/1741-7015-12-99).

3. Haskel J, Hughes A and Bascavusoglu-Moreau E, The Economic Significance of the UK Science Base, 2014, London: Campaign for Science and Engineering, http://www.sciencecampaign.org.uk/UKScienceBase.pdf (accessed October 2015).

4. Sussex J, Feng Y, Mestre-Ferrandiz J, et al., ‘Quantifying the economic impact of government and charity medical research on private R&D in the United Kingdom.’, BMC Medicine, 2016; 14:32, doi: 10.1186/s12916-016-0564-z.

5. Higher Education Funding Council for England, Research Excellence Framework 2014: The results, http://www.ref.ac.uk (accessed October 2015).

6. Pollitt A, Potoglou D, Patil S, et al., ‘Understanding the relative valuation of research impact: A best-worst scaling experiment of the general public and biomedical and health researchers’, Details TBC

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www.kcl.ac.uk/sspp/policy-institute @policyatkings