Centre for Economic and Social Research on Dementia, National University of Ireland Galway, Galway, Ireland.
Department of Public Health Midlands, Health Service Executive, Tullamore, Ireland.
Health Expect. 2021 Jun;24(3):800-809. doi: 10.1111/hex.13213. Epub 2021 Mar 2.
There are few examples of public patient involvement in policymaking for groups whose ability to participate may be affected by a disability, particularly for people with dementia and their family carers. Principles of engagement and inclusion in democratic processes are as important for these groups as other citizens. We used two innovative methods to increase involvement of people with dementia and family carers in the policymaking process in Ireland, specifically in relation to impending legislation on home care.
A Policy Café was co-produced with people with dementia using a World Café methodology. A Carer's Assembly was co-produced with caregivers of people with dementia using a citizen's assembly model.
Ten people with dementia discussed policy developments they wanted to see implemented in relation to diagnosis and home care. Twenty-eight dementia caregivers prioritized four topics: home care; respite services; psychosocial supports; and financial supports. Film and illustrations were used to create accessible messages for policy-makers to inform their decision making.
Involving people with dementia and carers in policy development requires time and creativity to facilitate and maximize their involvement. Co-production is essential to ensure the priorities of participants are identified, expressed and communicated effectively. A cumulative sequence of events and messages can generate significant engagement with policy-makers. Policy-makers need to hear the direct and authentic voice of people with dementia and carers when faced with important policy decisions.
People with dementia and carers were involved in study design, data analysis and presentation.
很少有公众参与制定政策的例子,特别是对于那些可能因残疾而影响参与能力的群体,例如痴呆症患者及其家庭照顾者。对于这些群体来说,参与和包容民主进程的原则与其他公民一样重要。我们使用了两种创新方法来增加爱尔兰痴呆症患者和家庭照顾者在决策过程中的参与度,特别是与即将出台的家庭护理立法有关。
我们与痴呆症患者共同制作了一个政策咖啡馆,使用了世界咖啡馆的方法。我们与痴呆症患者的照顾者共同制作了一个照顾者大会,使用了公民大会模式。
十名痴呆症患者讨论了他们希望看到在诊断和家庭护理方面实施的政策发展。二十八名痴呆症照顾者确定了四个优先事项:家庭护理;喘息服务;心理社会支持;和财政支持。电影和插图被用来为决策者制作可访问的信息,以帮助他们做出决策。
让痴呆症患者和照顾者参与政策制定需要时间和创造力来促进和最大限度地提高他们的参与度。共同制作对于确保参与者的优先事项得到识别、表达和有效沟通至关重要。一系列累积的事件和信息可以与决策者产生重大的互动。在面临重要政策决策时,决策者需要听到痴呆症患者和照顾者的直接和真实声音。
痴呆症患者和照顾者参与了研究设计、数据分析和演示。