AI Article Synopsis

  • A modified Delphi process was used to identify priorities for services and policies supporting caregivers of people living with dementia, focusing on historically underserved communities.
  • Participants (40 in total) completed three surveys that generated and ranked ideas across six key areas: care partner supports, programs, funding, information, care coordination, and workforce development.
  • The process emphasized participant knowledge and equal representation, encouraging diverse voices in decision-making, which could be applied to enhance engagement with dementia care partners.

Article Abstract

To determine priorities for services and policies that better support care partners of people living with dementia. A modified Delphi process engaged participants from organizations serving people living with dementia and care partners, focusing on historically and currently underserved communities. Eight thematic areas were identified. Participants ( = 40) responded to three surveys, generating ideas, rating each, and ranking priorities. Each survey received 13-17 responses. Top ranked ideas were arrayed across six thematic areas: care partner supports; programs; funding; information; care coordination; and workforce development. The Delphi process empowered participants to share knowledge, and respected their opinions. Anonymity removed power imbalances. The survey iterations blended qualitative and quantitative approaches, and built consensus. The Delphi invited the voices of diverse participants; all voices were weighed equally. This process could be extended to efforts to further engage dementia care partners, helping to value their voices in decision-making for services and policies.

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Source
http://dx.doi.org/10.1177/07334648241297130DOI Listing

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