Caring ahead: Mixed methods development of a questionnaire to measure caregiver preparedness for end-of-life with dementia

Author:

Durepos Pamela1ORCID,Akhtar-Danesh Noori2,Ploeg Jenny23,Sussman Tamara4,Kaasalainen Sharon2

Affiliation:

1. Faculty of Nursing, University of New Brunswick, Fredericton, NB, Canada

2. Faculty of Health Sciences, School of Nursing, McMaster University, Hamilton, ON, Canada

3. Aging, Community and Health Research Unit, Hamilton, ON, Canada

4. School of Social Work, McGill University, Montreal, QB, Canada

Abstract

Background: Family caregivers of persons with dementia often feel unprepared for end-of-life and preparedness predicts caregiver outcomes in bereavement. Existing questionnaires assessing preparedness have limitations. A multi-dimensional questionnaire assessing family caregiver preparedness for the end-of-life of persons with dementia is needed to identify caregivers at risk for negative outcomes in bereavement and evaluate the quality of strategies within a palliative approach. Aim: To develop a multi-dimensional questionnaire titled ‘Caring Ahead’ to assess feelings of preparedness for end-of-life in family caregivers of persons with dementia. Design: A mixed methods, sequential design employed semi-structured interviews, a Delphi-survey and pilot-testing of the questionnaire, June 2018 to July 2019. Setting/population: Participants included five current and 16 bereaved family caregivers of persons with symptoms advanced dementia from long-term care homes in Ontario, Canada; and 12 professional experts from clinical and academic settings in Canada, Europe, United States. Results: Interviews generated three core concepts and 114 indicators of preparedness sampling cognitive, affective and behavioural traits in four domains (i.e., medical, psychosocial, spiritual, practical). Indicators were translated and reduced to a pool of 73 potential questionnaire items. 30-items were selected to create the ‘Caring Ahead’ preparedness questionnaire through a Delphi-survey. Items were revised through a pilot-test with cognitive interviewing. Conclusions: Family caregivers’ feelings of preparedness for end-of-life need to be assessed and the quality of strategies within a palliative approach evaluated. Future psychometric testing of the Caring Ahead questionnaire will evaluate evidence for validity and reliability.

Funder

Canadian Nurses Foundation

Registered Nurses’ Association of Ontario

Alzheimer Society of Brant, Haldimand-Norfolk, Hamilton-Halton Branch

Institute of Health Services and Policy Research

Canadian Frailty Network Interdisciplinary Fellowship

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,General Medicine

Reference57 articles.

1. Dementia as a predictor of care-related quality of life in informal caregivers: a cross-sectional study to investigate differences in health-related outcomes between dementia and non-dementia caregivers

2. Family Caregivers' Strains

3. Health Canada. Framework on palliative care in Canada, https://www.canada.ca/content/dam/hc-sc/documents/services/health-care-system/reports-publications/palliative-care/framework-palliative-care-canada/framework-palliative-care-canada.pdf (2018, accessed 9 April 2020).

4. Public Health Agency of Canada. A dementia strategy for Canada: together we aspire, https://www.canada.ca/content/dam/phacaspc/images/services/publications/diseases-conditions/dementia-strategy/National%20Dementia%20Strategy_ENG.pdf (2019, accessed 9 April 2020).

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