Literature DB >> 21729411

Reasons why family members become carers and the outcome for the person with dementia: results from the CARD study.

Andrew Camden1, Gill Livingston, Claudia Cooper.   

Abstract

BACKGROUND: Using a representative secondary care survey for the first time, we explored family carers' reasons for providing care. We hypothesized that carers with a positive rather than negative motivation for caring would be less abusive towards the care recipient and more likely to be caring for someone still living at home a year later.
METHODS: We interviewed 220 consecutively referred dementia family/friend carers from UK Community Mental Health Teams. We asked non-spousal carers why they were the main carer. Our main outcomes were the revised Modified Conflict Tactics Scale scores, measuring abusive behavior by the carer, and admission of the person with dementia to a care home.
RESULTS: Nineteen (17.1%) said they were the main carer due to the high quality of their relationship with the care recipient, their willingness to take on or their suitability for the carer role. A further 22 (19.8%) said they were the main carer due to other potential carers' negative relationship with the care recipient, unwillingness or lack of suitability for the role. Carers who gave the latter explanation tended to be more anxious at baseline (F = 3.0, p = 0.055), reported higher abusive behavior towards the care recipient a year later after controlling for sociodemographic variables (t = 2.0, p = 0.05), and their care recipient was more likely to be admitted to a care home in the following year (hazards ratio 9.9, p = 0.040).
CONCLUSIONS: We found preliminary evidence that carers' reasons for providing care predict the well-being of the care recipient. Future studies involving dementia family carers should consider asking why the main carer assumed this role.

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Year:  2011        PMID: 21729411     DOI: 10.1017/S1041610211001189

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  6 in total

1.  Factor structure and construct validity of the Adult Social Care Outcomes Toolkit for Carers (ASCOT-Carer).

Authors:  Stacey E Rand; Juliette N Malley; Ann P Netten; Julien E Forder
Journal:  Qual Life Res       Date:  2015-06-03       Impact factor: 4.147

2.  Carers' quality of life and experiences of adult social care support in England.

Authors:  Stacey Rand; Juliette Malley
Journal:  Health Soc Care Community       Date:  2013-12-12

3.  Motivations for being informal carers of people living with dementia: a systematic review of qualitative literature.

Authors:  Nan Greenwood; Raymond Smith
Journal:  BMC Geriatr       Date:  2019-06-17       Impact factor: 3.921

Review 4.  How Culture Shapes Informal Caregiver Motivations: A Meta-Ethnographic Review.

Authors:  Mikołaj Zarzycki; Diane Seddon; Eva Bei; Rachel Dekel; Val Morrison
Journal:  Qual Health Res       Date:  2022-06-23

5.  Motivations and willingness to provide care from a geographical distance, and the impact of distance care on caregivers' mental and physical health: a mixed-method systematic review protocol.

Authors:  Eva Bei; Mikołaj Zarzycki; Val Morrison; Noa Vilchinsky
Journal:  BMJ Open       Date:  2021-07-07       Impact factor: 2.692

6.  Prevalence and Risk Factors of Abusive Behaviors in the Caregivers of People with Dementia in Korea.

Authors:  Taehyun Kim; Hyeon Jeong; Ji Won Han; Kyung Phil Kwak; Bong-Jo Kim; Shin-Kyeom Kim; Jeong Lan Kim; Tae Hui Kim; Seung-Ho Ryu; Seok Woo Moon; Jae Young Park; Joon Hyuk Park; Jae Nam Bae; Jong Chul Youn; Dong Young Lee; Dong Woo Lee; Seok Bum Lee; Jung Jae Lee; Jin Hyeong Jhoo; Jungwon Lee; Ki Woong Kim
Journal:  Psychiatry Investig       Date:  2018-07-04       Impact factor: 2.505

  6 in total

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