Health Expectations

Papers
(The median citation count of Health Expectations is 2. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-04-01 to 2024-04-01.)
ArticleCitations
Patient‐reported outcome measures (PROMs): A review of generic and condition‐specific measures and a discussion of trends and issues175
Understanding COVID‐19 misinformation and vaccine hesitancy in context: Findings from a qualitative study involving citizens in Bradford, UK153
Public preference for COVID‐19 vaccines in China: A discrete choice experiment103
Public attitudes towards COVID‐19 contact tracing apps: A UK‐based focus group study80
Mapping definitions of co‐production and co‐design in health and social care: A systematic scoping review providing lessons for the future63
Patients as partners in health research: A scoping review56
The challenges of caring for children who require complex medical care at home: ‘The go between for everyone is the parent and as the parent that’s an awful lot of responsibility’52
Factors explaining the fear of being infected with COVID‐1952
'Reluctant pioneer': A qualitative study of doctors' experiences as patients with long COVID52
The psychological burden of waiting for procedures and patient‐centred strategies that could support the mental health of wait‐listed patients and caregivers during the COVID‐19 pandemic: A scoping re46
Birth plan alterations among American women in response to COVID‐1946
Pragmatism as a paradigm for patient‐oriented research41
Shared decision making in surgery: A scoping review of the literature41
Mitigating unintended consequences of co‐design in health care37
Reflections, impact and recommendations of a co‐produced qualitative study with young people who have experience of mental health difficulties33
Patient and Public Involvement of young people with a chronic condition in projects in health and social care: A scoping review32
‘It struck at the heart of who I thought I was’: A meta‐synthesis of the qualitative literature examining the experiences of people with multiple sclerosis32
Mediated roles of generalized trust and perceived social support in the effects of problematic social media use on mental health: A cross‐sectional study32
How different health literacy dimensions influences health and well‐being among men and women: The mediating role of health behaviours32
Meaningful patient and public involvement in digital health innovation, implementation and evaluation: A systematic review32
The ultimate question? Evaluating the use of Net Promoter Score in healthcare: A systematic review31
Exploring invisibility and epistemic injustice in Long Covid—A citizen science qualitative analysis of patient stories from an online Covid community30
Trust, medical expertise and humaneness: A qualitative study on people with cancer’ satisfaction with medical care28
Revisiting patient expectations and experiences of antibiotics in an era of antimicrobial resistance: Qualitative study28
The manifestation of participation within a co‐design process involving patients, significant others and health‐care professionals26
Shared decision making in breast cancer treatment guidelines: Development of a quality assessment tool and a systematic review25
Do patient engagement interventions work for all patients? A systematic review and realist synthesis of interventions to enhance patient safety25
Comparative optimism about infection and recovery from COVID‐19; Implications for adherence with lockdown advice24
A systematic review of factors associated with side‐effect expectations from medical interventions23
Youth engagement in mental health research: A systematic review23
A scoping review of practice recommendations for clinicians’ communication of uncertainty22
Post‐discharge medicines management: the experiences, perceptions and roles of older people and their family carers22
Enhancing shared and surrogate decision making for people living with dementia: A systematic review of the effectiveness of interventions22
Participatory health research with migrants: Opportunities, challenges, and way forwards22
Shortening and validation of the Patient Engagement In Research Scale (PEIRS) for measuring meaningful patient and family caregiver engagement22
How to identify, incorporate and report patient preferences in clinical guidelines: A scoping review22
A national research centre for the evaluation and implementation of person‐centred care: Content from the first interventional studies21
Ensuring patient and public involvement in the transition to AI‐assisted mental health care: A systematic scoping review and agenda for design justice21
Patient involvement in interprofessional education: A qualitative study yielding recommendations on incorporating the patient’s perspective20
Determinants of patient activation and its association with cardiovascular disease risk in chronic kidney disease: A cross‐sectional study20
‘I don't know what to do or where to go’. Experiences of accessing healthcare support from the perspectives of people living with Long Covid and healthcare professionals: A qualitative study in Bradfo20
Reluctant educators and self‐advocates: Older trans adults’ experiences of health‐care services and practitioners in seeking gender‐affirming services20
Towards conceptual convergence: A systematic review of psychological resilience in family caregivers of persons living with chronic neurological conditions20
The experience of financial burden for people with multimorbidity: A systematic review of qualitative research19
An outbreak of appreciation: A discursive analysis of tweets of gratitude expressed to the National Health Service at the outset of the COVID‐19 pandemic19
How do health services engage culturally and linguistically diverse consumers? An analysis of consumer engagement frameworks in Australia19
Children's rights as law in Sweden–every health‐care encounter needs to meet the child's needs19
Barriers and facilitators to hepatitis C screening and treatment for people with lived experience of homelessness: A mixed‐methods systematic review19
Mapping the role of patient and public involvement during the different stages of healthcare innovation: A scoping review19
A co‐designed framework to support and sustain patient and family engagement in health‐care decision making19
COVID‐19 lockdown consequences on body mass index and perceived fragility related to physical activity: A worldwide cohort study18
Implementing culturally competent transplant care and implications for reducing health disparities: A prospective qualitative study18
Involving an individual with lived‐experience in a co‐analysis of qualitative data18
Experience of patients hospitalized with COVID‐19: A qualitative study of a pandemic disease in Iran18
Developing a patient safety guide for primary care: A co‐design approach involving patients, carers and clinicians17
Acceptability of risk‐stratified population screening across cancer types: Qualitative interviews with the Australian public17
Loss and recovery after concussion: Adolescent patients give voice to their concussion experience17
Is it worth it?: The experiences of persons with multiple sclerosis as they access health care to manage their condition17
Improving diversity in study participation: Patient perspectives on barriers, racial differences and the role of communities16
A qualitative study of health‐care experiences and challenges faced by ageing homebound adults16
Patient engagement in care: A scoping review of recently validated tools assessing patients' and healthcare professionals' preferences and experience16
More than a feeling? What does compassion in healthcare ‘look like’ to patients?16
Finding harmony within dissonance: Engaging patients, family/caregivers and service providers in research to fundamentally restructure relationships through integrative dynamics16
Evaluation of patient engagement in medicine development: A multi‐stakeholder framework with metrics16
An alternate level of care plan: Co‐designing components of an intervention with patients, caregivers and providers to address delayed hospital discharge challenges16
Patient and clinician perspectives on a patient‐facing dashboard that visualizes patient reported outcomes in rheumatoid arthritis16
Patient partners’ perspectives of meaningful engagement in synthesis reviews: A patient‐oriented rapid review15
A decision aid to support family carers of people living with dementia towards the end‐of‐life: Coproduction process, outcome and reflections15
Evaluation of a community dental clinic providing care to people experiencing homelessness: A mixed methods approach15
Talking the same language on patient empowerment: Development and content validation of a taxonomy of self‐management interventions for chronic conditions15
Approaches to optimize patient and family engagement in hospital planning and improvement: Qualitative interviews15
Adapting a codesign process with young people to prioritize outcomes for a systematic review of interventions to prevent self‐harm and suicide15
Adolescent and young adult patients as co‐researchers: A scoping review15
Priorities of patients, caregivers and health‐care professionals for health research – A systematic review15
The reported impact of public involvement in biobanks: A scoping review14
Sharing administrative health data with private industry: A report on two citizens' juries14
Applying the principles of adaptive leadership to person‐centred care for people with complex care needs: Considerations for care providers, patients, caregivers and organizations14
Patients' experiences of, and engagement with, remote home monitoring services for COVID‐19 patients: A rapid mixed‐methods study14
‘It reshaped how I will do research’: A qualitative exploration of team members’ experiences with youth and family engagement in a randomized controlled trial13
Experiences of self‐care during the COVID‐19 pandemic among individuals with rheumatoid arthritis: A qualitative study13
Genetic testing for hereditary cancer syndromes: patient recommendations for improved risk communication13
Renegotiating dimensions of the self: A systematic review and qualitative evidence synthesis of the lived experience of self‐managing rheumatoid arthritis13
Patient involvement in developing a patient‐targeted feedback intervention after depression screening in primary care within the randomized controlled trial GET.FEEDBACK.GP13
Understanding multi‐stakeholder needs, preferences and expectations to define effective practices and processes of patient engagement in medicine development: A mixed‐methods study13
Optimizing a digital intervention for managing blood pressure in stroke patients using a diverse sample: Integrating the person‐based approach and patient and public involvement13
‘I hated being ghosted’ – The relevance of social participation for living well with post‐stroke aphasia: Qualitative interviews with working aged adults13
Innovative methods for involving people with dementia and carers in the policymaking process13
Engagement of community stakeholders to develop a framework to guide research dissemination to communities12
Assessing and promoting partnership between patients and health‐care professionals: Co‐construction of the CADICEE tool for patients and their relatives12
Research‐ and health‐related youth advisory groups in Canada: An environmental scan with stakeholder interviews12
What does safety in mental healthcare transitions mean for service users and other stakeholder groups: An open‐ended questionnaire study12
‘Imposter participants’ in online qualitative research, a new and increasing threat to data integrity?12
Why don't patients seek help for chronic post‐surgical pain after knee replacement? A qualitative investigation12
Factors influencing oral health behaviours, access and delivery of dental care for autistic children and adolescents: A mixed‐methods systematic review12
How is patient‐centred care conceptualized in obstetrical health? comparison of themes from concept analyses in obstetrical health‐ and patient‐centred care12
'A limpet on a ship': Spatio‐temporal dynamics of patient and public involvement in research12
Insights into how Malaysian adults with limited health literacy self‐manage and live with asthma: A Photovoice qualitative study12
Seeking a deeper understanding of ‘distributed health literacy’: A systematic review12
Children's perspectives and experiences of the COVID‐19 pandemic and UK public health measures12
Advance care directive prevalence among older Australians and associations with person‐level predictors and quality indicators11
Patient perspectives on quality of care for depression and anxiety in primary health care teams: A qualitative study11
The CORE study—An adapted mental health experience codesign intervention to improve psychosocial recovery for people with severe mental illness: A stepped wedge cluster randomized‐controlled trial11
Mainstreaming public involvement in a complex research collaboration: A theory‐informed evaluation11
Improving primary health care quality for refugees and asylum seekers: A systematic review of interventional approaches11
Healthcare needs, experiences and treatment burden in primary care patients with multimorbidity: An evaluation of process of care from patients' perspectives11
Diabetes care provided by national standards can improve patients' self‐management skills: A qualitative study of how people with type 2 diabetes perceive primary diabetes care11
Improving the experience of older people with colorectal and breast cancer in patient‐centred cancer care pathways using experience‐based co‐design11
Ethical issues in participatory arts methods for young people with adverse childhood experiences11
A qualitative exploration of the barriers and facilitators affecting ethnic minority patient groups when accessing medicine review services: Perspectives of healthcare professionals11
Acceptability and potential impact on uptake of using different risk stratification approaches to determine eligibility for screening: A population‐based survey11
Patients as team members: Factors affecting involvement in treatment decisions from the perspective of patients with a chronic condition11
Caring for a sick or injured child during the COVID‐19 pandemic lockdown in 2020 in the UK: An online survey of parents' experiences11
Centredness in health care: A systematic overview of reviews11
‘They're getting a taste of our world’: A qualitative study of people with multiple sclerosis' experiences of accessing health care during the COVID‐19 pandemic in the Australian Capital Territory11
“I would not go to him”: Focus groups exploring community responses to a public health campaign aimed at reducing unnecessary diagnostic imaging of low back pain11
Reflections from the COVID‐19 pandemic on inequalities and patient and public involvement and engagement (PPIE) in social care, health and public health research11
Interdisciplinary communication and collaboration as key to improved nutritional care of malnourished older adults across health‐care settings – A qualitative study11
Utilizing patient advocates in Parkinson’s disease: A proposed framework for patient engagement and the modern metrics that can determine its success11
‘I think I will need help’: A systematic review of who facilitates the recovery from gender‐based violence and how they do so11
Aged care residents’ prioritization of care: A mixed‐methods study10
Adaptation and qualitative evaluation of Ask 3 Questions — a simple and generic intervention to foster patient empowerment10
Patient participation during primary health‐care encounters among adult patients with multimorbidity: A cross‐sectional study10
Doing involvement: A qualitative study exploring the ‘work’ of involvement enacted by older people and their carers during transition from hospital to home10
The impact of COVID‐19 on patient engagement in the health system: Results from a Pan‐Canadian survey of patient, family and caregiver partners10
Preference‐based patient participation for most, if not all: A cross‐sectional study of patient participation amongst persons with end‐stage kidney disease10
Stakeholder engagement from problem analysis to implementation strategies for a patient‐reported experience measure in disability care: A qualitative study on the process and experiences10
The involvement matrix as a framework for involving youth with severe communication disabilities in developing health education materials10
Power, recovery and doing something worthwhile: A thematic analysis of expert patient perspectives in psychiatry education10
The story vs the storyteller: Factors associated with the effectiveness of brief video‐recorded patient stories for promoting opioid tapering10
Living with opioids: A qualitative study with patients with chronic low back pain10
Can you see me? Participant experience of accessing a weight management programme via group videoconference to overcome barriers to engagement10
Performance of Thailand’s universal health coverage scheme: Evaluating the effectiveness of annual public hearings10
A patient and public involvement workshop using visual art and priority setting to provide patients with a voice to describe quality and safety concerns: Vitamin B12 deficiency and pernicious anaemia10
Refining a capability development framework for building successful consumer and staff partnerships in healthcare quality improvement: A coproduced eDelphi study10
No evidence synthesis about me without me: Involving young people in the conduct and dissemination of a complex evidence synthesis10
Physician behaviours that optimize patient‐centred care: Focus groups with migrant women10
Conceptualisations of positive mental health and wellbeing among children and adolescents in low‐ and middle‐income countries: A systematic review and narrative synthesis10
Views about integrating smoking cessation treatment within psychological services for patients with common mental illness: A multi‐perspective qualitative study9
Evaluating the effectiveness of the Family Connections program for caregivers of youth with mental health challenges, part I: A quantitative analysis9
Digital reminiscence app co‐created by people living with dementia and carers: Usability and eye gaze analysis9
Embedding lived experience into mental health academic research organizations: Critical reflections9
Discharge processes and medicines communication from the patient perspective: A qualitative study at an internal medicines ward in Norway9
A community jury study exploring the public acceptability of using risk stratification to determine eligibility for cancer screening9
An exercise intervention for people with serious mental illness: Findings from a qualitative data analysis using participatory theme elicitation9
A qualitative exploration of oral health care among stroke survivors living in the community9
An engaged approach to exploring issues around poverty and mental health: A reflective evaluation of the research process from researchers and community partners involved in the DeStress study9
‘A lot of small things make a difference’. Mental health and strategies of coping during the COVID‐19 pandemic9
Training in health coaching skills for health professionals who work with people with progressive neurological conditions: A realist evaluation9
Nothing about us without us: A co‐production strategy for communities, researchers and stakeholders to identify ways of improving health and reducing inequalities9
Online community engagement in response to COVID‐19 pandemic9
Perceived barriers and facilitators to exercise in kidney transplant recipients: A qualitative study9
A qualitative evaluation of coproduction of research: ‘If you do it properly, you will get turbulence’9
Patient and researcher experiences of patient engagement in primary care health care research: A participatory qualitative study8
Codesigning person‐centred quality indicators with diverse communities: A qualitative patient engagement study8
The chronic disease Self‐Management Programme: A phenomenological study for empowering vulnerable patients with chronic diseases included in the EFFICHRONIC project8
Health literacy experiences of multi‐ethnic patients and their health‐care providers in the management of type 2 diabetes in Malaysia: A qualitative study8
The socioemotional challenges and consequences for caregivers of Aboriginal and Torres Strait Islander children with otitis media: A qualitative study8
Stuff you think you can handle as a parent and stuff you can’t’. Understanding parental health‐seeking behaviour when accessing unscheduled care: A qualitative study8
In the works: Patient and public involvement and engagement in healthcare decision‐making8
‘Advocacy groups are the connectors’: Experiences and contributions of rare disease patient organization leaders in advanced neurotherapeutics8
The Ecology of Engagement: Fostering cooperative efforts in health with patients and communities8
Giving an account of patients' experience: A qualitative study on the care process of hip and knee osteoarthritis8
Applying Patient and Public Involvement in preclinical research: A co‐created scoping review8
Navigating dietary advice for multiple sclerosis8
Barriers and enabling factors in weight management of patients with nonalcoholic fatty liver disease: A qualitative study using the COM‐B model of behaviour8
Experiences of and attitudes to lifestyle modification for the management of multiple sclerosis: A qualitative analysis of free‐text survey data8
‘It's not magic’: A qualitative analysis of geriatric physicians' explanations of cardio‐pulmonary resuscitation in hospital admissions8
Adapting patient and public involvement in patient‐oriented methods research: Reflections in a Canadian setting during COVID‐198
INNOVATE Research: Impact of a workshop to develop researcher capacity to engage youth in research8
Use of co‐design methodology in the development of cardiovascular disease secondary prevention interventions: A scoping review8
Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation8
Humanizing harm: Using a restorative approach to heal and learn from adverse events8
Experiences of cervical screening participation and non‐participation in women from minority ethnic populations in Scotland8
Participatory codesign of patient involvement in a Learning Health System: How can data‐driven care be patient‐driven care?8
A mapping and synthesis of tools for stakeholder and community engagement in quality improvement initiatives for reproductive, maternal, newborn, child and adolescent health8
Ask us! Adjusting experience‐based codesign to be responsive to people with intellectual disabilities, serious mental illness or older persons receiving support with independent living8
Perceptions of patients undergoing percutaneous coronary intervention on pre‐operative education in China: A qualitative study8
Cross‐cultural validation of the patient‐practitioner orientation scale among primary care professionals in Spain8
Barriers and facilitators of shared decision making in acutely ill inpatients with schizophrenia—Qualitative findings from the intervention group of a randomised‐controlled trial7
How might diabetes organisations address diabetes‐related stigma? Findings from a deliberative democratic case study7
‘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 Domains7
Creative Long Covid: A qualitative exploration of the experience of Long Covid through the medium of creative narratives7
Partnering with older people as peer researchers7
The impact of Patient and Public Involvement in the SlowMo study: Reflections on peer innovation7
Chronic and rare disease patients' access to healthcare services during a health crisis: The example of the COVID‐19 pandemic in Turkey7
Patients with low activation level report limited possibilities to participate in cancer care7
It takes three to tango: An ethnography of triadic involvement of residents, families and nurses in long‐term dementia care7
‘He or she maybe doesn't know there is such a thing as a review’: A qualitative investigation exploring barriers and facilitators to accessing medication reviews from the perspective of people from et7
Providing culturally safe care to Indigenous people living with diabetes: Identifying barriers and enablers from different perspectives7
Tailored patient therapeutic educational interventions: A patient‐centred communication model7
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review7
'It just wasn’t going to be heard’: A mixed methods study to compare different ways of involving people with diabetes and health‐care professionals in health intervention research7
The Wellness Quest: A health literacy and self‐advocacy tool developed by youth for youth mental health7
Patient experiences of the urgent cancer referral pathway—Can the NHS do better? Semi‐structured interviews with patients with upper gastrointestinal cancer7
What are the underlying reasons behind socioeconomic differences in doctor‐patient communication in head and neck oncology review clinics?7
Development of a patient decision aid for patients with breast cancer who consider immediate breast reconstruction after mastectomy7
Mapping the experiences of people with achalasia from initial symptoms to long‐term management7
Conducting public involvement in dementia research: The contribution of the European Working Group of People with Dementia to the ROADMAP project7
Advancing understanding of influences on cervical screening (non)‐participation among younger and older women: A qualitative study using the theoretical domains framework and the COM‐B model7
Knowledge sharing to support long‐term condition self‐management—Patient and health‐care professional perspectives7
The experiences of men following recurrent miscarriage in an Irish tertiary hospital: A qualitative analysis7
The impact of prenatal counselling on mothers of surviving children with hypoplastic left heart syndrome: A qualitative interview study7
Adolescents and young adults’ (AYA) views on their cancer knowledge prior to diagnosis: Findings from a qualitative study involving AYA receiving cancer care7
Exploring motivations and resistances for implementing shared decision‐making in clinical practice: A systematic review based on a structure–process–outcome model7
Reporting the whole story: Analysis of the ‘out‐of‐scope’ questions from the James Lind Alliance Teenage and Young Adult Cancer Priority Setting Partnership Survey7
‘Triadic’ shared decision making in mental health: Experiences and expectations of service users, caregivers and clinicians in Germany7
Proposals for person‐centred care in the COVID‐19 era. Delphi study7
Beneficial self‐management support and user involvement in Healthy Life Centres—A qualitative interview study in persons afflicted by overweight or obesity7
Characteristics of the ideal healthcare services to meet adolescents' mental health needs: A qualitative study of adolescents' perspectives7
More ‘milk’ than ‘psychology or tablets’: Mental health professionals’ perspectives on the value of peer support workers7
Enhancing community weight loss groups in a low socioeconomic status area: Application of the COM‐B model and Behaviour Change Wheel7
Changes in public perceptions and experiences of the Australian health‐care system: A decade of change7
Shared decision making in consultations for hypertension: Qualitative study in general practice6
Barriers and facilitators to mobile health and active surveillance use among older adults with skin disease6
Assessing the efficacy of coproduction to better understand the barriers to achieving sustainability in NHS chronic kidney services and create alternate pathways6
Multiple stakeholders' perspectives on patient and public involvement in community mental health services research: A qualitative analysis6
Perceptions of aquatic physiotherapy and health‐related quality of life among people with Parkinson’s disease6
Development of the Pharm‐SAVES educational module for gatekeeper suicide prevention training for community pharmacy staff6
Beyond the control of the care home: A meta‐ethnography of qualitative studies of Infection Prevention and Control in residential and nursing homes for older people6
Outcomes of importance to children and young adults with cerebral palsy, their parents and health professionals following lower limb orthopaedic surgery: A qualitative study to inform a Core Outcome S6
What's Up With Everyone? A qualitative study on young people's perceptions of cocreated online animations to promote mental health literacy6
Involving patients in research during a pandemic6
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ6
Experiences, perceptions and expectations of health services amongst marginalized populations in urban Australia: A meta‐ethnographic review of the literature6
Seeking or contributing? Evidence of knowledge sharing behaviours in promoting patients’ perceived value of online health communities6
Prioritizing Chinese medicine clinical research questions in cancer palliative care from patient and caregiver perspectives6
A qualitative study of nurse‐patient communication and information provision during surgical pre‐admission clinics6
Adapting a conceptual framework to engage diverse stakeholders in genomic/precision medicine research6
Using social media for patient and public involvement and engagement in health research: The process and impact of a closed Facebook group6
Development of a novel gout treatment patient decision aid by patient and physician: A qualitative research study6
Public acceptability of public health policy to improve population health: A population‐based survey6
Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic6
Barriers to employment of Australian cancer survivors living with geographic or socio‐economic disadvantage: A qualitative study6
Perceptions, needs and preferences of chronic disease self‐management support among men experiencing homelessness in Montreal6
Delivery of supported self‐management in remote asthma reviews: A systematic rapid realist review6
Information, deliberation, and decisional control preferences for participation in medical decision‐making and its influencing factors among Chinese cancer patients6
Question prompt lists and endorsement of question‐asking support patients to get the information they seek—A longitudinal qualitative study6
Co‐ideation and co‐design in co‐creation research: Reflections from the ‘Co‐Creating Safe Spaces’ project6
Patients' experiences of behaviour change interventions delivered by general practitioners during routine consultations: A nationally representative survey6
Co‐design development of a decision guide on eating and drinking for people with severe dementia during acute hospital admissions6
Exploring a collaborative approach to the involvement of patients, carers and the public in the initial education and training of healthcare professionals: A qualitative study of patient experiences6
Engaging young people within a collaborative knowledge mobilization network: Development and evaluation6
Cultural adaptation of a community‐based advance serious illness planning decision aid to the Quebec context involving end‐users6
Improving the depth of data quality or increasing confusion? Reflections on a data analysis involving members of a self‐help group for relatives of people living with dementia6
Patient, clinician and manager experience of the accelerated implementation of virtual consultations following COVID‐19: A qualitative study of preferences in a tertiary orthopaedic rehabilitation set6
Reducing delayed transfer of care in older people: A qualitative study of barriers and facilitators to shorter hospital stays6
The revised Patient Perception of Patient‐Centeredness Questionnaire: Exploring the factor structure in French‐speaking patients with multimorbidity6
Sociocultural influences on asthma self‐management in a multicultural society: A qualitative study amongst Malaysian adults6
The SWIM study: Ethnic minority women's ideas and preferences for a tailored intervention to promote national cancer screening programmes—A qualitative interview study6
"Care is not care if it isn't person‐centred": A content analysis of how Person‐Centred Care is expressed on Twitter6
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