What are the essential features of resilience for informal caregivers of people living with dementia? A Delphi consensus examination

Joling, K.J. and Windle, G. and Droes, R.M. and Huisman, M. and Hertogh, C. and Woods, R.T. (2015) What are the essential features of resilience for informal caregivers of people living with dementia? A Delphi consensus examination. Aging and Mental Health. DOI: 10.1080/13607863.2015.1124836

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OBJECTIVES: Few studies have examined what might enable or prevent resilience in carers of people with dementia. Consequently, there are limited insights as to how it should be understood, defined and measured. This creates challenges for research, and also practice in terms of how it might best be promoted. This study aimed to address these limitations and add new insights, identifying the essential features of resilience in dementia caregiving. METHODS: A Delphi consensus study was conducted, consulting a multi-disciplinary panel of informal caregivers and experts with relevant professional expertise. Panellists rated the relevance of various statements addressing essential components of resilience; 'adversity' and 'successful caregiving' on a 5-point Likert scale. Based on the median and Inter Quartile Range, the most relevant statements with moderate consensus were proposed in Round 2 in which panellists selected up to five statements in order of importance. RESULTS: Moderate consensus was reached for all statements after two rounds. Patients' behavioural problems and feeling competent as a caregiver were selected by both caregivers and professionals as essential resilience features. Caregivers also emphasized the importance of social support, the quality of the relationship with their relative and enjoying spending time together. Professionals considered coping skills, experiencing positive aspects of caregiving, and a good quality of life of caregivers most relevant. CONCLUSION: The essential elements of resilience selected from multiple stakeholder perspectives can be used to select appropriate outcomes for intervention studies and give guidance to policy to support caregivers more effectively and better tailored to their needs.

Item Type: Article
Subjects: Research Publications
Departments: College of Health and Behavioural Sciences > Institute of Medical & Social Care Research
Date Deposited: 23 Oct 2015 02:08
Last Modified: 22 Jan 2016 03:19
ISSN: 1360-7863
URI: http://e.bangor.ac.uk/id/eprint/5704
Identification Number: DOI: 10.1080/13607863.2015.1124836
Publisher: Taylor & Francis
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