Josie Dixon considers a paired-cluster randomised controlled trial of an advance care planning intervention, called the Family Carer Decision Support (FCDS) intervention, undertaken by Kevin Brazil and colleagues (2018) in dementia nursing homes.
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Vaso Totsika’s blog considers a study by Crane and colleagues, which seeks to further our understanding of how young autistic people experience the world of service provision in relation to their mental health needs, and in particular at the time of transition from child to adult services.
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Jill Manthorpe’s blog considers findings from a scoping review and institutional ethnography of the ‘information work’ done by family carers of community-dwelling older adults living with dementia, by Dalmer (2018).
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Kate Baxter reviews a study by Trigg et al. (2018) which explores and compares the type and quantity of information that makes people feel comfortable when choosing a residential care home in the UK, Netherlands and Spain.
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Francesca Pozzoli considers a qualitative metasynthesis of directly funded home-care programmes for older people and the concept of ‘choice’.
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Jo Moriarty’s blog looks at parents and volunteers’ experiences of Home-Start, a family support programme, via the theoretical framework of liminality.
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Mike Clark’s blog considers a paper in which the authors reflect on tensions arising in the coproduction of adult social care evaluation between the participatory research approach and validated outcome measures.
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Bruce McClure’s blog looks at a feasibility study of ‘LifeFul’, a reablement programme in the care home context.
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Martin Webber looks at a systematic review and meta-analysis of studies reporting on the association between informal carers’ sense of coherence, caregiver burden and mental health outcomes.
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Mark Holloway considers a scoping review of the social work‐generated evidence base on people with traumatic brain injury (TBI) of working age.
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