An exploration of the cultural appropriateness of the family-centered function-focused care intervention

Author:

BeLue Rhonda1ORCID,Kuzmik Ashley2ORCID,Dix Michaila3ORCID,Luckett Camille45ORCID,Paudel Anju2ORCID,Resnick Barbara5,Boltz Marie2ORCID

Affiliation:

1. College for Health, Community and Policy, Community Engagement and Partnerships, The University of Texas at San Antonio, USA

2. Ross and Carol Nese College of Nursing, Penn State, USA

3. College of Public Health and Social Justice, Department of Health Management and Policy, Saint Louis University, USA

4. College for Public Health and Social Justice, Saint Louis University, USA

5. University of Maryland School of Nursing, USA

Abstract

The Family-centered Function Focused Care (Fam-FFC) intervention, is a nurse-family care partnership model aimed to improve the physical and cognitive recovery in hospitalized persons living with Alzheimer’s Disease Related Dementias (ADRD) while improving the care partner’s experiences. Discussions of patients’ needs and preferences between nurses and the patient’s close family members have been found to be useful in preventing excessive stress in persons with dementia, while lessening the anxiety of care partners. However, the efficacy of dementia-specific interventions is influenced in part by the degree to which the interventions are flexible and sensitive to the patient’s and care-partner’s condition, needs, and preferences, including cultural preferences. Therefore, the purpose of this study is to assess the cultural appropriateness of Fam-FFC using the Ecological Validity Model (EVM). This qualitative, descriptive study included 28 consented care partners drawn from a sample of 455 dyads enrolled in the Fam-FFC intervention. An interview guide was created based on the EVM. Participants provided demographic data. Thematic analysis was conducted to analyze transcribed interviews. The majority of the sample was female (79%), Non-Hispanic (96%) and half were married. One-half of the sample represented Black care partners and one-half were White. Seventy-nine percent lived with their family member with ADRD. Three major themes were identified from the thematic analysis including Care Partner Identity, Care Partner Preferences, and Goals of Care for functional recovery of their family member living with dementia. In this study care partners wanted more social services as well as home care that supported not just physical needs but also social and recreational needs. Findings from the study offer guidance on improving the Fam-FFC intervention including strengthening education and resources on partner self-care.

Funder

National institute of Aging, National Institutes of Health

Publisher

SAGE Publications

Subject

General Social Sciences,Sociology and Political Science,General Medicine

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