Clarissa Giebel summarises a recent systematic review that investigates the effectiveness of various psychotherapies (CBT, interpersonal therapy, counselling) for depression and anxiety in people with dementia or mild cognitive impairment.
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Earlier this year, we posted about a study which showed positive outcomes being achieved by suitable persons for individuals lacking capacity to consent to direct payments.
Here Alex Leeder, who blogged about this study, looks at the views of parent-carers who have fulfilled the role of ‘suitable person’ – an ‘insider’ perspective.
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Sarah Carr looks at a literature review assessing how choice is working for family carers in the context of social care personalisation.
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Jeanne Carlin discusses a review about influences on adult children carers’ well-being and thinks about what the evidence means for Care Act implementation.
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Caroline Struthers is frustrated by the lack of high quality research identified by this recent review, which looks at interventions to improve the experience and well-being of those caring for people with severe mental illness.
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What are the experiences of families who are supporting their adult sons and daughters with learning disabilities to move on to their own homes?
Here, Mandy Johnson looks at a study, which sets out to answer that question.
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Lack of sleep for parents has been associated with depression, stress and anxiety and sleep problems for parents of children with learning disabilities are common.
Here, Rachel Allen looks at an evaluation of the effectiveness of a sleep management intervention that was delivered through support to groups of parents.
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In this blog, Ermintrude looks at secondary analysis of carer surveys and discusses the findings on hours of unpaid care in the context of obligations under the Care Act.
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How do staff and family carers recognise when somebody they support is in pain and what emotional impact does this have on them?
Here, Nick Burton looks at a small scale qualitative study, which set out to explore this issue for some paid carers and family carers.
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People with learning disabilities are living longer than ever before, so more people are likely to need palliative care services and end-of-life care.
Here, Fawn Harrad looks at a study, which set out to listen specifically to the views of people with a learning disability and family carers in receipt of palliative care services.
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