A review of the factors associated with the non-use of respite services by carers of people with dementia: Implications for policy and practice

Findings

#ResourceNotFound: OAPLabels, EvidenceSummary#

Evidence Summary
Supporting technical documents that are social systems-relevant

Not usually available for this document type
Full-text report

Full-text report (free)
Scientific Abstract

PubMed
Scientific Abstract

Publisher

Recency, quality and context of the findings

Last year literature searched

2011
Year Published

2014
Quality Rating

4/9 (AMSTAR rating from McMaster Health Forum)
Countries in which studies (included in the synthesis) were conducted

USA (10); Canada (2); Australia (1); Germany (1)
Global/regional focus

WHO - Americas region<br />WHO - European region<br />WHO - Western Pacific region<br />
Country focus

USA (10); Canada (2); Australia (1); Germany (1)
Low - and middle-income country (LMIC) focus

Additional details about the research

Type of document

Systematic review addressing other questions
Type of question

Not effectiveness
Focus

Specific
Target

Individual
Family/household
Community
Domain

Programs and services
Community and social services
Other social services
Sustainable Development Goals
3. Good health and well-being (partially covered)
17. Partnerships for the goals
Social system topic(s)

Delivery arrangements
How services are designed to meet citizens’ needs
Culturally appropriate services
Package of services/service pathways
Where services are provided
Outreach
Implementation strategies
Citizen-targeted strategy
Behaviour change support
(Personal) Support
Theme

Optimal aging

Publication details

Citation

Phillipson L, Jones SC, Magee C. A review of the factors associated with the non-use of respite services by carers of people with dementia: Implications for policy and practice. Health & Social Care in the Community. 2014;22(1):1-12.
DOI

10.1111/hsc.12036

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