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Predictors of the psychosocial impact of being a carer of people living with Parkinson's disease: A systematic review

Predictors of the psychosocial impact of being a carer of people living with Parkinson's disease: A systematic review
Predictors of the psychosocial impact of being a carer of people living with Parkinson's disease: A systematic review
INTRODUCTION:
Caring for a person with Parkinson's disease (PwP) can have a variety of negative consequences that may challenge their ability to continue their caring role. It is still unknown why some individuals adapt better than others in response to such burdens. This review is the first to synthesize and evaluate the evidence on the predictive factors of psychosocial outcomes in PwP carers.
METHODS:
Studies which identified predictors of psychosocial outcomes for unpaid carers were included. PsychINFO, EMBASE, AMED, BNI and CINAHL databases were searched, supplemented by scanning of references lists of included studies and relevant journals from 2008 onwards. Quality was assessed using the NICE methodology checklist for prognostic studies.
RESULTS:
Twenty-nine studies were included in the review, providing a low-level of evidence. Carer burden was investigated in 18 studies and mental health and quality of life (QoL) in seven studies each. PwP non-motor symptoms and QoL and carer depression were consistently identified as predictors for at least one psychosocial outcome. Demographics and disease factors were consistently found not to be predictors. Carer involvement and protective factors (e.g. social support, personality) demonstrated promising findings but studies were too few or factors measured inconsistently.
CONCLUSION:
Confident conclusions could not be drawn regarding the most important predictors that should be targeted in psychosocial interventions due to methodological weaknesses and lack of theoretical testing across the current literature. Future research should build upon psychological theory to gain a better understanding of the mechanisms that explain how carers adapt to caregiving.
1353-8020
1-11
Greenwell, Kate
4bac64bd-059f-4d7d-90d3-5c0bccb7ffb2
Gray, William K.
930d5430-e9b6-45a6-9483-7b82b7b49633
van Wersch, Anna
b7f902dc-adbc-416f-b46e-3f1315907b16
van Schaik, Paul
9546ed8d-e702-4f4c-a9d7-7af2510c925c
Walker, Richard
154d32d9-fc45-44fb-b2c2-9a7f21130c08
Greenwell, Kate
4bac64bd-059f-4d7d-90d3-5c0bccb7ffb2
Gray, William K.
930d5430-e9b6-45a6-9483-7b82b7b49633
van Wersch, Anna
b7f902dc-adbc-416f-b46e-3f1315907b16
van Schaik, Paul
9546ed8d-e702-4f4c-a9d7-7af2510c925c
Walker, Richard
154d32d9-fc45-44fb-b2c2-9a7f21130c08

Greenwell, Kate, Gray, William K., van Wersch, Anna, van Schaik, Paul and Walker, Richard (2015) Predictors of the psychosocial impact of being a carer of people living with Parkinson's disease: A systematic review. Parkinsonism and Related Disorders, 21 (1), 1-11. (doi:10.1016/j.parkreldis.2014.10.013).

Record type: Article

Abstract

INTRODUCTION:
Caring for a person with Parkinson's disease (PwP) can have a variety of negative consequences that may challenge their ability to continue their caring role. It is still unknown why some individuals adapt better than others in response to such burdens. This review is the first to synthesize and evaluate the evidence on the predictive factors of psychosocial outcomes in PwP carers.
METHODS:
Studies which identified predictors of psychosocial outcomes for unpaid carers were included. PsychINFO, EMBASE, AMED, BNI and CINAHL databases were searched, supplemented by scanning of references lists of included studies and relevant journals from 2008 onwards. Quality was assessed using the NICE methodology checklist for prognostic studies.
RESULTS:
Twenty-nine studies were included in the review, providing a low-level of evidence. Carer burden was investigated in 18 studies and mental health and quality of life (QoL) in seven studies each. PwP non-motor symptoms and QoL and carer depression were consistently identified as predictors for at least one psychosocial outcome. Demographics and disease factors were consistently found not to be predictors. Carer involvement and protective factors (e.g. social support, personality) demonstrated promising findings but studies were too few or factors measured inconsistently.
CONCLUSION:
Confident conclusions could not be drawn regarding the most important predictors that should be targeted in psychosocial interventions due to methodological weaknesses and lack of theoretical testing across the current literature. Future research should build upon psychological theory to gain a better understanding of the mechanisms that explain how carers adapt to caregiving.

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More information

Accepted/In Press date: 10 October 2014
e-pub ahead of print date: 22 October 2014
Published date: January 2015

Identifiers

Local EPrints ID: 415477
URI: http://eprints.soton.ac.uk/id/eprint/415477
ISSN: 1353-8020
PURE UUID: 10542c73-0834-4cf8-a4ac-97b3a7d373c4
ORCID for Kate Greenwell: ORCID iD orcid.org/0000-0002-3662-1488

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Date deposited: 10 Nov 2017 17:31
Last modified: 16 Mar 2024 04:28

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Contributors

Author: Kate Greenwell ORCID iD
Author: William K. Gray
Author: Anna van Wersch
Author: Paul van Schaik
Author: Richard Walker

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