In her debut blog, Pooja Saini summarises a recent qualitative study that explored access to care for older adults who self-harm. The blog contains some excellent recommendations for primary care professionals and policy-makers.
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In her debut blog, Zoë Catchpole summarises a recent qualitative paper about the Australian #chatsafe project, which outlines how young people were involved in the development of an online campaign to support conversations about suicide.
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Simon D’Alfonso summarises an editorial by Sarah Carr, which places the patient as a “domain expert” in artificial intelligence mental health research.
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Andrew Shepherd explores a paper that makes him ask: Does the language and implementation of evidence based practice essentially risk excluding different voices from mental heath policy making?
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Shuichi Suetani and Sharon Lawn explore a recent viewpoint article on physical health problems in psychosis, which asks: Is it time to consider the views of family carers?
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Caroline Struthers considers a systematic review about the impacts of older people’s patient and public involvement in health and social care research.
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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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Laura Hemming summarises a literature review of how best to involve forensic service users in research, which highlights a number of issues specific to the forensic setting.
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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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Lucy Simons highlights the RAPPORT study and the importance of strong relationships between PPI (patient and public involvement) representatives and researchers, which are seen to be essential for PPI to become normal practice in research.
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