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SCI Abstract
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Testing the effects on information use by older versus younger women of modality and narration style in a hospital report card
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Engaging young people within a collaborative knowledge mobilization network: Development and evaluation
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Demographics, health literacy and health locus of control beliefs of Australian women who take complementary medicine products during pregnancy and breastfeeding: A cross‐sectional, online, national survey
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Exploring the expectations, experiences and tensions of refugee patients and general practitioners in the quality of care in general practice
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Expectations of a new opt‐out system of consent for deceased organ donation in England: A qualitative interview study
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Adolescents encouraging healthy lifestyles through a peer‐led social marketing intervention: Training and key competencies learned by peer leaders
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‘A lot of small things make a difference’. Mental health and strategies of coping during the COVID‐19 pandemic
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Swallowing the pill of adverse effects: A qualitative study of patients' and pharmacists' experiences and decision‐making regarding the adverse effects of chronic pain medications
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‘You have to do what is best’: The lived reality of having a child who is repeatedly hospitalized because of acute lower respiratory infection
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Patients at the centre after a health care incident: A scoping review of hospital strategies targeting communication and nonmaterial restoration
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Part of the solution: A survey of community organisation perspectives on barriers and facilitating actions to Advance Care Planning in British Columbia, Canada
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Qualitative investigation of factors impacting pre‐exposure prophylaxis initiation and adherence in sexual minority men
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Experiences, perceptions and expectations of health services amongst marginalized populations in urban Australia: A meta‐ethnographic review of the literature
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Conceptualisations of positive mental health and wellbeing among children and adolescents in low‐ and middle‐income countries: A systematic review and narrative synthesis
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Capturing learning from public involvement with people experiencing homelessness to help shape new physiotherapy research: Utilizing a reflective model with an under‐served, vulnerable population
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A framework for involving coproduction partners in research about young people with type 1 diabetes
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Engaging veteran stakeholders to identify patient‐centred research priorities for optimizing implementation of lung cancer screening
Abstract Background Patient engagement in research agenda setting is increasingly being seen as a strategy to improve the ...
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The lived experience of a novel disruptive therapy in a group of men and boys with haemophilia A with inhibitors: Emi & Me
Abstract Background People with haemophilia A and inhibitors (PwHi) suffer more orthopaedic complications, bleeding and pa...
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The relative importance of information items and preferred mode of delivery when disseminating results from trials to participants: A mixed‐methods study
Abstract Background Participants want to receive the results of trials that they have participated in. Dissemination pract...
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Views of healthcare consumer representatives on defensive practice: ‘We are your biggest advocate and supporter… not the enemy’
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‘I just thought that it was such an impossible thing’: A qualitative study of barriers and facilitators to discontinuing long‐term use of benzodiazepine receptor agonists using the Theoretical Domains Framework
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Barriers and facilitators to hepatitis C screening and treatment for people with lived experience of homelessness: A mixed‐methods systematic review
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Development and field testing of a decision aid to facilitate shared decision making for adults newly diagnosed with attention‐deficit hyperactivity disorder
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How paediatric departments in Sweden facilitate giving children a voice on their experiences of healthcare: A cross‐sectional study
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