Results: 92

For: service user involvement

EQUIPment testing: evaluating a co-delivered care planning training programme

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Sarah Carr treats us to a bumper blog of EQUIP studies. Think: care planning, coproduction, service user involvement and training. She doesn’t blog for us very often these days, but when she does it’s a corker!

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Recovering Quality of Life (ReQOL) scale: a PROM you don’t want to miss

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Martina Sawicka and Derek Tracy take a look at the ReQOL scale (Recovering Quality of Life): a patient reported outcome measure (PROM) for use with people experiencing mental health difficulties.

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Digital Technology for Mental Health: asking the right questions #DigitalMHQ

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Lucy Simons invites YOU to tell us what you think are the most important questions about using digital technology for mental health.

There are also some fab prizes up for grabs, so don’t miss out!

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Patients included? Twitter impact at health care conferences

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Amy Price considers the impact that patient participation can have at health care conferences: increased information flow, greater reach and impact, and deeper engagement in the conversation of tweets compared to physicians or researchers.

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Power to the people: practitioners, patients and power

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Rob Allison explores a recent qualitative study of dependence and resistance in community mental health care, which looks at negotiations of user participation between mental health staff and service users.

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Do we need a Truth and Reconciliation process in psychiatry?

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Sarah Carr and Danny Taggart explore the case for truth and reconciliation in psychiatry and mental health services. It’s a really thought-provoking blog that all mental health service users, survivors, refusers and professionals should read.

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What happened to you? Trauma informed approaches to mental health care

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Sarah Carr explores a narrative review of trauma informed approaches to mental health care, which aims to provide a definition and plan for future development.

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What does patient and public involvement feel like?

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Alison Turner explores a recent study of patient and public involvement in clinical commissioning, which found that PPI representatives are often uncertain about their role and how their contribution is used.

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A social model for understanding madness and distress

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Alison Faulkner on a new Shaping Our Lives report, which addresses service user and survivor views about ways of understanding madness and distress, but in particular about the potential of a social model.

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