Findings From a Real-World Translation Study of the Evidence-Based “Partners in Dementia Care”

Author:

Bass David M1,Hornick Thomas2,Kunik Mark345,Judge Katherine S15,Primetica Branka1,Kearney Keith1,Rentsch Julie1,Mccarthy Catherine1,Grim Jennifer6

Affiliation:

1. Center for Research and Education, Benjamin Rose Institute on Aging, Cleveland, Ohio

2. Louis Stokes Department of Veterans Affairs Medical Center, Cleveland, Ohio

3. Houston Center for Quality of Care & Utilization Studies, Texas

4. Veterans Affairs South Central Mental Illness Research, Education and Clinical Center, Houston, Texas

5. Department of Psychology, Cleveland State University, Ohio

6. NAMI Wayne and Holmes Counties, Canton, Ohio

Abstract

Abstract Background and Objectives Numerous non-pharmacological programs for family caregivers and persons with dementia (PWDs) have been found efficacious in randomized controlled trials. Few programs have been tested in translation studies that assess feasibility and outcomes in less-controlled, real-world implementations. This translation study tested the impact of the partnership version of BRI Care Consultation, “Partners in Dementia Care (PDC),” on outcomes for PWDs and their family/friend caregivers. PDC was delivered via partnerships between the Louis Stokes Department of Veterans Affairs Medical Center and the Greater East Ohio Alzheimer’s Association Chapter and the Western Reserve Area Agency on Aging. PDC is a personalized coaching program done by telephone, e-mail, and regular mail. Research Design and Methods For this translation study, the program was implemented in a manner that mirrored a non-research implementation. The study sample included 148 caregivers and 84 PWDs who used PDC for 12 months. Research data came from 2 structured telephone interviews, one before program implementation and a follow-up after program completion. PWDs and caregivers averaged 14 telephone contacts with Care Consultants over the 12-month study period, and 12 behavioral action steps to address problems or concerns. Results Repeated measures ANOVAs showed the use of PDC was related to significant improvements across several outcomes for PWDs and caregivers, with greater benefits in more difficult caregiving situations. Caregivers had decreased levels of isolation, physical health strain, unmet needs; and increased confidence in caregiving capacity, informal helpers, and support service use. PWDs had decreased embarrassment about memory problems and unmet needs; and increased informal support and community service use. Discussion and Implications Overall, improved outcomes for PWDs and caregivers in this translation study were similar to findings from previous randomized trials, and affirmed the value of the program when delivered as a regular service offering by health care and community service organizations.

Funder

Ohio’s Dementia Capable Systems Integration Grant, Part B, Administration on Community Living

Administration on Aging, Ohio’s Unified Prevention and Long-Term Care System Initiative

Publisher

Oxford University Press (OUP)

Subject

Life-span and Life-course Studies,Health Professions (miscellaneous),Health (social science)

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