Health Expectations

Article	Citations
Patient‐reported outcome measures (PROMs): A review of generic and condition‐specific measures and a discussion of trends and issues	258
Understanding COVID‐19 misinformation and vaccine hesitancy in context: Findings from a qualitative study involving citizens in Bradford, UK	165
Public preference for COVID‐19 vaccines in China: A discrete choice experiment	110
Mapping definitions of co‐production and co‐design in health and social care: A systematic scoping review providing lessons for the future	95
Public attitudes towards COVID‐19 contact tracing apps: A UK‐based focus group study	85
Patients as partners in health research: A scoping review	62
Pragmatism as a paradigm for patient‐oriented research	61
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 re	57
Factors explaining the fear of being infected with COVID‐19	57
'Reluctant pioneer': A qualitative study of doctors' experiences as patients with long COVID	57
The ultimate question? Evaluating the use of Net Promoter Score in healthcare: A systematic review	46
Meaningful patient and public involvement in digital health innovation, implementation and evaluation: A systematic review	44
Mitigating unintended consequences of co‐design in health care	42
Mediated roles of generalized trust and perceived social support in the effects of problematic social media use on mental health: A cross‐sectional study	42
Youth engagement in mental health research: A systematic review	41
Exploring invisibility and epistemic injustice in Long Covid—A citizen science qualitative analysis of patient stories from an online Covid community	39
‘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 Bradfo	36
How different health literacy dimensions influences health and well‐being among men and women: The mediating role of health behaviours	36
Trust, medical expertise and humaneness: A qualitative study on people with cancer’ satisfaction with medical care	33
Do patient engagement interventions work for all patients? A systematic review and realist synthesis of interventions to enhance patient safety	33
‘Imposter participants’ in online qualitative research, a new and increasing threat to data integrity?	32
Ensuring patient and public involvement in the transition to AI‐assisted mental health care: A systematic scoping review and agenda for design justice	32
Shortening and validation of the Patient Engagement In Research Scale (PEIRS) for measuring meaningful patient and family caregiver engagement	31
Participatory health research with migrants: Opportunities, challenges, and way forwards	31
Determinants of patient activation and its association with cardiovascular disease risk in chronic kidney disease: A cross‐sectional study	29

The manifestation of participation within a co‐design process involving patients, significant others and health‐care professionals	29
Towards conceptual convergence: A systematic review of psychological resilience in family caregivers of persons living with chronic neurological conditions	29
A scoping review of practice recommendations for clinicians’ communication of uncertainty	29
Enhancing shared and surrogate decision making for people living with dementia: A systematic review of the effectiveness of interventions	27
Barriers and facilitators to hepatitis C screening and treatment for people with lived experience of homelessness: A mixed‐methods systematic review	25
Involving an individual with lived‐experience in a co‐analysis of qualitative data	25
More than a feeling? What does compassion in healthcare ‘look like’ to patients?	25
Post‐discharge medicines management: the experiences, perceptions and roles of older people and their family carers	24
Improving diversity in study participation: Patient perspectives on barriers, racial differences and the role of communities	24
Patients' experiences of, and engagement with, remote home monitoring services for COVID‐19 patients: A rapid mixed‐methods study	24
The experience of financial burden for people with multimorbidity: A systematic review of qualitative research	23
Experience of patients hospitalized with COVID‐19: A qualitative study of a pandemic disease in Iran	22
Mapping the role of patient and public involvement during the different stages of healthcare innovation: A scoping review	21
Patient engagement in care: A scoping review of recently validated tools assessing patients' and healthcare professionals' preferences and experience	21
Acceptability of risk‐stratified population screening across cancer types: Qualitative interviews with the Australian public	21
Adapting a codesign process with young people to prioritize outcomes for a systematic review of interventions to prevent self‐harm and suicide	20
A decision aid to support family carers of people living with dementia towards the end‐of‐life: Coproduction process, outcome and reflections	20
An outbreak of appreciation: A discursive analysis of tweets of gratitude expressed to the National Health Service at the outset of the COVID‐19 pandemic	20
Children's perspectives and experiences of the COVID‐19 pandemic and UK public health measures	20
COVID‐19 lockdown consequences on body mass index and perceived fragility related to physical activity: A worldwide cohort study	20
Patient partners’ perspectives of meaningful engagement in synthesis reviews: A patient‐oriented rapid review	20
Developing a patient safety guide for primary care: A co‐design approach involving patients, carers and clinicians	20
Implementing culturally competent transplant care and implications for reducing health disparities: A prospective qualitative study	20
Loss and recovery after concussion: Adolescent patients give voice to their concussion experience	20
How do health services engage culturally and linguistically diverse consumers? An analysis of consumer engagement frameworks in Australia	20
Applying the principles of adaptive leadership to person‐centred care for people with complex care needs: Considerations for care providers, patients, caregivers and organizations	20
Evaluation of patient engagement in medicine development: A multi‐stakeholder framework with metrics	20
Optimizing a digital intervention for managing blood pressure in stroke patients using a diverse sample: Integrating the person‐based approach and patient and public involvement	19
Factors influencing oral health behaviours, access and delivery of dental care for autistic children and adolescents: A mixed‐methods systematic review	19
Talking the same language on patient empowerment: Development and content validation of a taxonomy of self‐management interventions for chronic conditions	18
Adolescent and young adult patients as co‐researchers: A scoping review	18
Nothing about us without us: A co‐production strategy for communities, researchers and stakeholders to identify ways of improving health and reducing inequalities	18
‘I hated being ghosted’ – The relevance of social participation for living well with post‐stroke aphasia: Qualitative interviews with working aged adults	18
Improving primary health care quality for refugees and asylum seekers: A systematic review of interventional approaches	17
Approaches to optimize patient and family engagement in hospital planning and improvement: Qualitative interviews	17
Healthcare needs, experiences and treatment burden in primary care patients with multimorbidity: An evaluation of process of care from patients' perspectives	17
Innovative methods for involving people with dementia and carers in the policymaking process	17
Understanding multi‐stakeholder needs, preferences and expectations to define effective practices and processes of patient engagement in medicine development: A mixed‐methods study	16
Embedding lived experience into mental health academic research organizations: Critical reflections	15
Navigating dietary advice for multiple sclerosis	15
‘It reshaped how I will do research’: A qualitative exploration of team members’ experiences with youth and family engagement in a randomized controlled trial	15
Patients as team members: Factors affecting involvement in treatment decisions from the perspective of patients with a chronic condition	15
Advance care directive prevalence among older Australians and associations with person‐level predictors and quality indicators	15
How is patient‐centred care conceptualized in obstetrical health? comparison of themes from concept analyses in obstetrical health‐ and patient‐centred care	15
Seeking a deeper understanding of ‘distributed health literacy’: A systematic review	15
Sharing administrative health data with private industry: A report on two citizens' juries	15
Patient and researcher experiences of patient engagement in primary care health care research: A participatory qualitative study	14
Experiences of self‐care during the COVID‐19 pandemic among individuals with rheumatoid arthritis: A qualitative study	14
‘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 Territory	14
Evaluating the effectiveness of the Family Connections program for caregivers of youth with mental health challenges, part I: A quantitative analysis	14

Aged care residents’ prioritization of care: A mixed‐methods study	14
Assessing and promoting partnership between patients and health‐care professionals: Co‐construction of the CADICEE tool for patients and their relatives	14
‘Advocacy groups are the connectors’: Experiences and contributions of rare disease patient organization leaders in advanced neurotherapeutics	14
Preference‐based patient participation for most, if not all: A cross‐sectional study of patient participation amongst persons with end‐stage kidney disease	14
'A limpet on a ship': Spatio‐temporal dynamics of patient and public involvement in research	14
Caring for a sick or injured child during the COVID‐19 pandemic lockdown in 2020 in the UK: An online survey of parents' experiences	14
Research‐ and health‐related youth advisory groups in Canada: An environmental scan with stakeholder interviews	14
“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 pain	14
Applying Patient and Public Involvement in preclinical research: A co‐created scoping review	13
Patient participation during primary health‐care encounters among adult patients with multimorbidity: A cross‐sectional study	13
Ethical issues in participatory arts methods for young people with adverse childhood experiences	13
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 model	13
Reflections from the COVID‐19 pandemic on inequalities and patient and public involvement and engagement (PPIE) in social care, health and public health research	13
The impact of COVID‐19 on patient engagement in the health system: Results from a Pan‐Canadian survey of patient, family and caregiver partners	13
Perceived barriers and facilitators to exercise in kidney transplant recipients: A qualitative study	13
Doing involvement: A qualitative study exploring the ‘work’ of involvement enacted by older people and their carers during transition from hospital to home	13
Tailored patient therapeutic educational interventions: A patient‐centred communication model	13
Experiences of and attitudes to lifestyle modification for the management of multiple sclerosis: A qualitative analysis of free‐text survey data	13
Conceptualisations of positive mental health and wellbeing among children and adolescents in low‐ and middle‐income countries: A systematic review and narrative synthesis	13
Patient perspectives on quality of care for depression and anxiety in primary health care teams: A qualitative study	13
Centredness in health care: A systematic overview of reviews	13
A qualitative evaluation of coproduction of research: ‘If you do it properly, you will get turbulence’	13
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	13
Improving the experience of older people with colorectal and breast cancer in patient‐centred cancer care pathways using experience‐based co‐design	13
Acceptability and potential impact on uptake of using different risk stratification approaches to determine eligibility for screening: A population‐based survey	12
Power, recovery and doing something worthwhile: A thematic analysis of expert patient perspectives in psychiatry education	12
A qualitative exploration of the barriers and facilitators affecting ethnic minority patient groups when accessing medicine review services: Perspectives of healthcare professionals	12
Performance of Thailand’s universal health coverage scheme: Evaluating the effectiveness of annual public hearings	12
Insights into how Malaysian adults with limited health literacy self‐manage and live with asthma: A Photovoice qualitative study	12
Refining a capability development framework for building successful consumer and staff partnerships in healthcare quality improvement: A coproduced eDelphi study	12
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 trial	12
What does safety in mental healthcare transitions mean for service users and other stakeholder groups: An open‐ended questionnaire study	12
The use of arts‐based methodologies and methods with young people with complex psychosocial needs: A systematic narrative review	12
A community jury study exploring the public acceptability of using risk stratification to determine eligibility for cancer screening	12
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	12
Can you see me? Participant experience of accessing a weight management programme via group videoconference to overcome barriers to engagement	11
Online community engagement in response to COVID‐19 pandemic	11
The involvement matrix as a framework for involving youth with severe communication disabilities in developing health education materials	11
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 care	11
The story vs the storyteller: Factors associated with the effectiveness of brief video‐recorded patient stories for promoting opioid tapering	11
Knowledge sharing to support long‐term condition self‐management—Patient and health‐care professional perspectives	11
Stakeholder engagement from problem analysis to implementation strategies for a patient‐reported experience measure in disability care: A qualitative study on the process and experiences	11
The Ecology of Engagement: Fostering cooperative efforts in health with patients and communities	11
Giving an account of patients' experience: A qualitative study on the care process of hip and knee osteoarthritis	11
‘I think I will need help’: A systematic review of who facilitates the recovery from gender‐based violence and how they do so	11
Barriers and enabling factors in weight management of patients with nonalcoholic fatty liver disease: A qualitative study using the COM‐B model of behaviour	11
Changes in public perceptions and experiences of the Australian health‐care system: A decade of change	11
Humanizing harm: Using a restorative approach to heal and learn from adverse events	11
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 anaemia	11
Use of co‐design methodology in the development of cardiovascular disease secondary prevention interventions: A scoping review	11
‘A lot of small things make a difference’. Mental health and strategies of coping during the COVID‐19 pandemic	11
Participatory codesign of patient involvement in a Learning Health System: How can data‐driven care be patient‐driven care?	11
Digital reminiscence app co‐created by people living with dementia and carers: Usability and eye gaze analysis	10
Development of a patient decision aid for patients with breast cancer who consider immediate breast reconstruction after mastectomy	10
Experiences of cervical screening participation and non‐participation in women from minority ethnic populations in Scotland	10
In the works: Patient and public involvement and engagement in healthcare decision‐making	10
Barriers and facilitators of shared decision making in acutely ill inpatients with schizophrenia—Qualitative findings from the intervention group of a randomised‐controlled trial	10
Partnering with older people as peer researchers	10
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 interpretation	10
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 study	10
‘It's not magic’: A qualitative analysis of geriatric physicians' explanations of cardio‐pulmonary resuscitation in hospital admissions	10
The impact of Patient and Public Involvement in the SlowMo study: Reflections on peer innovation	10
Discharge processes and medicines communication from the patient perspective: A qualitative study at an internal medicines ward in Norway	10
The chronic disease Self‐Management Programme: A phenomenological study for empowering vulnerable patients with chronic diseases included in the EFFICHRONIC project	10
An exercise intervention for people with serious mental illness: Findings from a qualitative data analysis using participatory theme elicitation	10
Ask us! Adjusting experience‐based codesign to be responsive to people with intellectual disabilities, serious mental illness or older persons receiving support with independent living	9
Cross‐cultural validation of the patient‐practitioner orientation scale among primary care professionals in Spain	9
Using social media for patient and public involvement and engagement in health research: The process and impact of a closed Facebook group	9
Patients with low activation level report limited possibilities to participate in cancer care	9
Understanding support systems for Parkinson's disease management in community settings: A cross‐national qualitative study	9
Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID‐19 pandemic	9
The Youth Patient and Public Involvement Café—A youth‐led model for meaningful involvement with children and young people	9
Enhancing community weight loss groups in a low socioeconomic status area: Application of the COM‐B model and Behaviour Change Wheel	9
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	9
The role of advocacy and empowerment in shaping service development for families raising children with developmental disabilities	9
A qualitative study exploring the benefits of involving young people in mental health research	9
‘Triadic’ shared decision making in mental health: Experiences and expectations of service users, caregivers and clinicians in Germany	9
Transitional care for patients with acute stroke—A priority‐setting project	9
More ‘milk’ than ‘psychology or tablets’: Mental health professionals’ perspectives on the value of peer support workers	9
‘Corona is coming’: COVID‐19 vaccination perspectives and experiences amongst Culturally and Linguistically Diverse West Australians	9

Patient views on asthma diagnosis and how a clinical decision support system could help: A qualitative study	9
Views about integrating smoking cessation treatment within psychological services for patients with common mental illness: A multi‐perspective qualitative study	9
Barriers and facilitators to mobile health and active surveillance use among older adults with skin disease	9
Development of the Engage with Impact Toolkit: A comprehensive resource to support the evaluation of patient, family and caregiver engagement in health systems	9
Exploring motivations and resistances for implementing shared decision‐making in clinical practice: A systematic review based on a structure–process–outcome model	9
Co‐design development of a decision guide on eating and drinking for people with severe dementia during acute hospital admissions	9
Codesigning person‐centred quality indicators with diverse communities: A qualitative patient engagement study	9
It takes three to tango: An ethnography of triadic involvement of residents, families and nurses in long‐term dementia care	9
Providing culturally safe care to Indigenous people living with diabetes: Identifying barriers and enablers from different perspectives	9
A mapping and synthesis of tools for stakeholder and community engagement in quality improvement initiatives for reproductive, maternal, newborn, child and adolescent health	9
‘Lifts your spirits, lifts your mind’: A co‐produced mixed‐methods exploration of the benefits of green and blue spaces for mental wellbeing	8
Rapid development of a COVID‐19 care planning decision‐aid for family carers of people living with dementia	8
Effectiveness of a structured short intervention against stigmatisation in chronic visible skin diseases: Results of a controlled trial in future educators	8
Co‐ideation and co‐design in co‐creation research: Reflections from the ‘Co‐Creating Safe Spaces’ project	8
Women's experiences along the ovarian cancer diagnostic pathway in Catalonia: A qualitative study	8
Shared decision making in consultations for hypertension: Qualitative study in general practice	8
Perceptions of patients undergoing percutaneous coronary intervention on pre‐operative education in China: A qualitative study	8
What are the underlying reasons behind socioeconomic differences in doctor‐patient communication in head and neck oncology review clinics?	8
Proposals for person‐centred care in the COVID‐19 era. Delphi study	8
‘Down to the person, the individual patient themselves’: A qualitative study of treatment decision‐making for shoulder pain	8
Characteristics of the ideal healthcare services to meet adolescents' mental health needs: A qualitative study of adolescents' perspectives	8
Patient and general practitioner experiences of implementing a medication review intervention in older people with multimorbidity: Process evaluation of the SPPiRE trial	8
Delivery of supported self‐management in remote asthma reviews: A systematic rapid realist review	8
Adolescents and young adults’ (AYA) views on their cancer knowledge prior to diagnosis: Findings from a qualitative study involving AYA receiving cancer care	8
‘No‐one has listened to anything I’ve got to say before’: Co‐design with people who are sleeping rough	8
‘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	8
A qualitative study of nurse‐patient communication and information provision during surgical pre‐admission clinics	8
Question prompt lists and endorsement of question‐asking support patients to get the information they seek—A longitudinal qualitative study	8
Chronic and rare disease patients' access to healthcare services during a health crisis: The example of the COVID‐19 pandemic in Turkey	8
Mapping the experiences of people with achalasia from initial symptoms to long‐term management	8
Patient perspectives on primary care for multimorbidity: An integrative review	8
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 people	8
Barriers to employment of Australian cancer survivors living with geographic or socio‐economic disadvantage: A qualitative study	8
How paediatric departments in Sweden facilitate giving children a voice on their experiences of healthcare: A cross‐sectional study	8
What's Up With Everyone? A qualitative study on young people's perceptions of cocreated online animations to promote mental health literacy	8
Introducing and integrating perinatal mental health screening: Development of an equity‐informed evidence‐based approach	8
The Wellness Quest: A health literacy and self‐advocacy tool developed by youth for youth mental health	8
Widening or narrowing inequalities? The equity implications of digital tools to support COVID‐19 contact tracing: A qualitative study	8
Adapting a conceptual framework to engage diverse stakeholders in genomic/precision medicine research	8
Adapting patient and public involvement in patient‐oriented methods research: Reflections in a Canadian setting during COVID‐19	8
Exploring the impact of engagement in mental health and substance use research: A scoping review and thematic analysis	8
Evaluating the role and effectiveness of co‐produced community‐based mental health interventions that aim to reduce suicide among adults: A systematic review	8
Development and content validity of the Experienced Patient‐Centeredness Questionnaire (EPAT)—A best practice example for generating patient‐reported measures from qualitative data	8
The socioemotional challenges and consequences for caregivers of Aboriginal and Torres Strait Islander children with otitis media: A qualitative study	8
‘They need to ask me first’. Community engagement with low‐income citizens. A realist qualitative case‐study	8
The experiences of men following recurrent miscarriage in an Irish tertiary hospital: A qualitative analysis	8
Sociocultural influences on asthma self‐management in a multicultural society: A qualitative study amongst Malaysian adults	7
How might diabetes organisations address diabetes‐related stigma? Findings from a deliberative democratic case study	7
User involvement in the making: Positions and types of knowledge enacted in the interaction between service users and researchers in user panel meetings	7
Factors influencing decisions people with motor neuron disease make about gastrostomy placement and ventilation: A qualitative evidence synthesis	7
Multiple stakeholders' perspectives on patient and public involvement in community mental health services research: A qualitative analysis	7
The lived experiences of women exploring a healthy lifestyle, gestational weight gain and physical activity throughout pregnancy	7
The effects of a mobile application for patient participation to improve patient safety	7
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 dementia	7
‘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 et	7
The lived experience of a novel disruptive therapy in a group of men and boys with haemophilia A with inhibitors: Emi & Me	7
Reporting the whole story: Analysis of the ‘out‐of‐scope’ questions from the James Lind Alliance Teenage and Young Adult Cancer Priority Setting Partnership Survey	7
The development of a culturally sensitive educational video: How to facilitate informed decisions on cervical cancer screening among Turkish‐ and Moroccan‐Dutch women	7
Accompanying patients in clinical oncology teams: Reported activities and perceived effects	7
Experiences, perceptions and expectations of health services amongst marginalized populations in urban Australia: A meta‐ethnographic review of the literature	7
Information, deliberation, and decisional control preferences for participation in medical decision‐making and its influencing factors among Chinese cancer patients	7
Social support services for dementia during the COVID‐19 pandemic: A longitudinal survey exploring service adaptations in the United Kingdom	7
‘What price do you put on your health?’: Medical cannabis, financial toxicity and patient perspectives on medication access in advanced cancer	7
Epistemic justice in public involvement and engagement: Creating conditions for impact	7
Engaging young people within a collaborative knowledge mobilization network: Development and evaluation	7
Conducting public involvement in dementia research: The contribution of the European Working Group of People with Dementia to the ROADMAP project	7
An intervention of sustainable weight change: Influence of self‐help group and expectations	7
What adults with ADHD want to know: A Delphi consensus study on the psychoeducational needs of experts by experience	7
Clinician perspectives on clinical decision support systems in lung cancer: Implications for shared decision‐making	7
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 S	7
Creative Long Covid: A qualitative exploration of the experience of Long Covid through the medium of creative narratives	7
Reducing delayed transfer of care in older people: A qualitative study of barriers and facilitators to shorter hospital stays	7
Patients' experiences of behaviour change interventions delivered by general practitioners during routine consultations: A nationally representative survey	7
Health‐care professionals’ assessment of a person‐centred intervention to empower self‐management and health across chronic illness: Qualitative findings from a process evaluation study	7
Interactional practices in person‐centred care: Conversation analysis of nurse‐patient disagreement during self‐management support	7
Exploring patient acceptability of a short‐stay care pathway in hospital post arthroplasty: A theory‐informed qualitative study	7
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 experiences	7
Reconsidering patient‐centred care: Authority, expertise and abandonment	7
Perceptions of aquatic physiotherapy and health‐related quality of life among people with Parkinson’s disease	7
Cultural adaptation of a community‐based advance serious illness planning decision aid to the Quebec context involving end‐users	7
Using cocreated visually informed community mental health education in low‐ and middle‐income countries: A case study of youth substance misuse in Assam, India	7
Patients' experiences across the trajectory of atrial fibrillation: A qualitative systematic review	7
Family caregiver roles and challenges in assisting patients with cancer treatment decision‐making: Analysis of data from a national survey	7
Experiences and expectations of receiving volunteer services among home‐based elderly in Chinese urban areas: A qualitative study	7
“Whilst you are here…” Acceptability of providing advice about screening and early detection of other cancers as part of the breast cancer screening programme	7
Tools to evaluate medication management for caregivers of people living with dementia: A systematic review	7
Prioritizing Chinese medicine clinical research questions in cancer palliative care from patient and caregiver perspectives	6
Priorities and preferences for care of people with multiple chronic conditions	6
Awareness of diagnosis, treatment and risk of late effects in Chinese survivors of childhood cancer in Hong Kong	6
Operationalizing a patient engagement plan for health research: Sharing a codesigned planning template from a national clinical trial	6
"Care is not care if it isn't person‐centred": A content analysis of how Person‐Centred Care is expressed on Twitter	6
Reimagining consumer involvement: Resilient system indicators in the COVID‐19 pandemic response in New South Wales, Australia	6
Towards an Implementation‐STakeholder Engagement Model (I‐STEM) for improving health and social care services	6
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	6
Seeking or contributing? Evidence of knowledge sharing behaviours in promoting patients’ perceived value of online health communities	6