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January 23, 2026Health Expectations0 citationsOpen Access

Involving Societal Stakeholders in Dementia Risk Reduction: An Explorative Study

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JDJolanda H. M. DobbeSESmets EmEKEsmee Kreuk

Key Points

  • This study aims to identify societal stakeholders for dementia risk reduction and explore their perspectives.
  • Qualitative approach with participatory research elements
  • Advisory panel of citizens for input on the research
  • Two-phase data collection: stakeholder identification and perspective exploration
  • 18 interviews and one focus group with 32 participants
  • Thematic analysis of the data collected.
  • Participants had limited knowledge and responsibility for dementia risk reduction
  • Calls for policy changes to prioritize dementia risk reduction
  • Recommendations for integrating dementia information into general health campaigns
  • Emphasis on early life strategies for dementia risk reduction.

Abstract

ABSTRACT Objectives Optimal dementia risk reduction requires a combination of individual‐ and population‐level approaches. Societal stakeholders play a crucial role by raising awareness, supporting individual lifestyle change, and/or influencing certain risk factors through policy changes. This study aimed to identify relevant societal stakeholders for promoting dementia risk reduction, and explore perspectives regarding their role. Methods We used a qualitative approach with participatory research elements (i.e., collaborating with stakeholders in the research). An advisory panel of citizens ( n = 14) was installed to provide input on various study aspects (e.g., study design and interpretation of findings). Thereafter, data collection involved two phases: 1) identification of potentially relevant societal stakeholders (based on advisory panel discussions, a conference workshop, and online searches); and 2) exploration of perspectives of participants from selected stakeholder domains, through 18 interviews and one focus group (total N = 32). We analysed data using thematic analysis. Results Phase 2 revealed that participants, such as religious leaders, labour service employees and board members of student associations, had limited knowledge and experienced little responsibility to act as a societal stakeholder in the context of dementia risk reduction. Rather, they called for policy and regulations to make dementia risk reduction efforts obligatory and a public priority. Participants recommended incorporating information on dementia and dementia risk in general health campaigns, rather than organising dementia‐specific campaigns, and stressed the need to stimulate dementia risk reduction early in life. Conclusions Effective dementia risk reduction could benefit from increased stakeholder involvement, as well as imposed policy‐level risk reduction measures. Our findings also highlight the importance of including dementia in education and healthy lifestyle programmes from an early age. Future studies are needed to validate our findings on a larger scale, and among different stakeholders. Patient or Public Contribution Citizens were involved in study conceptualisation and design, and in the interpretation, reporting and dissemination of findings.

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Cite This Study

Dobbe et al. (2026) studied this question.

synapsesocial.com/papers/69731047c8125b09b0d1ff8ehttps://doi.org/10.1111/hex.70541
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