Health Expectations

Article	Citations
Issue Information	376
Patient preferences for heart valve disease intervention	177
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	134
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Inside Front Cover: Volume 25 Issue 1	85
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	74
Development of an inflammatory bowel disease (IBD) Patient‐Reported Experience Measure (PREM): A patient‐led consensus work and ‘think aloud’ study for a quality improvement programme	72
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	67
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	58
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	57
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	56
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	56
Feasibility of a best–worst scaling exercise to set priorities for autism research	54
Indicators for adequate diabetes care for the indigenous communities of Ecuador	52
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	46
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	44
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	41
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	41
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	38
Preferences for Peer Support Amongst Families Engaged in Paediatric Screening Programmes: The Perspectives of Parents Involved in Screening for Type 1 Diabetes in Children Aged 3–13	36
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	34
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	31
Just a story? Leadership, lived experience and integrated care	31
Participatory research with carers: A systematic review and narrative synthesis	31
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	31

Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	29
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	28
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	28
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs	26
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	26
Youth engagement in mental health research: A systematic review	25
Developing a novel co‐produced methodology to understand ‘real‐world’ help‐seeking in online peer–peer communities by young people experiencing emotional abuse and neglect	25
‘Physical well‐being is our top priority’: Healthcare professionals' challenges in supporting psychosocial well‐being in stroke services	24
‘Language has been granted too much power’.1,p.1 Challenging the power of words with time and flexibility in the precommencement stage of research involving those with cognitive impairment	24
The experiences of psychiatric patients, their caregivers and companions in upholding patient dignity during hospitalization: A qualitative study	24
Exploring the lived experience of receiving mental health crisis care at emergency departments, crisis phone lines and crisis care alternatives	24
Experiences and expectations of receiving volunteer services among home‐based elderly in Chinese urban areas: A qualitative study	23
Person‐centred caregiver singing for people living with dementia in South Africa: A mixed methods evaluation of acceptability, feasibility, and professional caregivers' experiences	23
How we define recurrent miscarriage matters: A qualitative exploration of the views of people with professional or lived experience	23
The interactive dimensions of encounters in HIV care: From trauma to relational traumatic growth	23
All Good Without Anything Good. Beyond Survival: Understanding the Psychosocial Experiences of Individuals With Chronic Kidney Disease and Their Caregivers in Sri Lanka	23
Behaviour, barriers and facilitators of shared decision making in breast cancer surgical treatment: A qualitative systematic review using a ‘Best Fit’ framework approach	23
Physical Health Checks and Follow‐Up Care in Deprived and Ethnically Diverse People With Severe Mental Illness: Co‐Designed Recommendations for Better Care	22
‘I Have Never Been in That Kind of All‐Consuming Pain … I Did Not Know What Else to Do’: The Journey to Hospital Admission With Low Back Pain From the Perspectives of Patients	22
Patient and Staff Insights on Digital Care Pathways for Patients With Low Back Pain in the Emergency Department: A Qualitative Study	22
Announcements of Death During the COVID‐19 Pandemic: A Qualitative Study of Family Experiences	22
‘But … Would I Be Able to Toast With Friends?’ When Service Users Ask for New Care Pathways	22
Enhancing community weight loss groups in a low socioeconomic status area: Application of the COM‐B model and Behaviour Change Wheel	22
Content validity testing of the INTERMED Self‐Assessment in a sample of adults with rheumatoid arthritis and rheumatology healthcare providers	22
Assessing the environment for engagement in health services: The Audit for Consumer Engagement (ACE) tool	21
Viewpoints among experts and the public in the Netherlands on including a lifestyle criterion in the healthcare priority setting	21
Reflections on the opportunities and challenges of applying experience‐based co‐design (EBCD) to phase 1 clinical trials in oncology	20
Knowledge Families Hold: Co‐Production and Co‐Research With Mental Health Family Carers in Understanding Experiences During the COVID‐19 Pandemic	20
Evaluation of aspiration risk by relatives of inpatients in the neurology service: A metaphor analysis	20
Agenda Setting in Outpatient Consultation of Older Adults With Long‐COVID	20
Self‐directed self‐management interventions to prevent or address distress in young people with long‐term physical conditions: A rapid review	20
‘Lifts your spirits, lifts your mind’: A co‐produced mixed‐methods exploration of the benefits of green and blue spaces for mental wellbeing	19
The Challenging Process of Developing an Antenatal Social Intervention for Parents From Culturally Diverse Backgrounds to Reduce Postnatal Distress: A Participatory Action Research Study	19
‘They need to ask me first’. Community engagement with low‐income citizens. A realist qualitative case‐study	19
Needs assessment for health service design for people with back pain in a hospital setting: A qualitative study	19
HIV Care Seeking Pathways and Barriers to the Continuum of Care Faced by Persons Living With HIV in Rural Nepal: A Qualitative Study	19
Patient perspectives on quality of care for depression and anxiety in primary health care teams: A qualitative study	18
Family Interviews Improve Health Service Recommendations in Mortality Review Process: A Mixed‐Methods Assessment	18
Co‐design of the EMBED‐Care Framework as an intervention to enhance shared decision‐making for people affected by dementia and practitioners, comprising holistic assessment, linked with clinical decis	18
Development of person‐centred quality indicators for aged care assessment services in Australia: A mixed methods study	18
Gender bias in shared decision‐making among cancer care guidelines: A systematic review	18
Delivery of supported self‐management in remote asthma reviews: A systematic rapid realist review	18
Patient perspectives on primary care for multimorbidity: An integrative review	18
Problem‐based shared decision making: The role of canonical SDM steps	17
Consumer Experience of an Australian Multidisciplinary Long COVID Clinic That Incorporates Personalised Exercise Prescription: A Qualitative Analysis	17
Understanding the cultural environment of the outpatient care setting for patients with dementia receiving cancer treatment: A qualitative study	17
Experiences and Perceptions of Self‐Harm in Rural‐Dwelling Adults: A Rapid Review of Qualitative Evidence	17
A Community Jury on initiating weight management conversations in primary care	17
The HUSH Project: Using codesign to reduce sleep disruptions for patients in hospital	17
Co‐Creation in Research: Further Reflections From the ‘Co‐Creating Safe Spaces’ Project	16

Women's experiences of care after stillbirth and obstetric fistula: A phenomenological study in Kenya	16
The Co‐Production, Pilot and Qualitative Evaluation of a Cancer Prevention Programme With High‐Risk Women Delivered on Group Walks by Cancer Champions: Shoulder to Shoulder, Walk and Talk	16
Participatory approaches for developing a practical handbook integrating health information for supporting individuals with mild cognitive impairment and their families	16
Developing a Women's Thought Collective methodology for health research: The roles and responsibilities of researchers in the reflexive co‐production of knowledge	16
Social Determinants as Mediators of the Emotional State of People With Type 2 Diabetes and/or Hypertension During the COVID‐19 Pandemic in Ecuador and Spain	16
Co‐production and adaptation of a prison‐based problem‐solving workbook to support the mental health of patients housed within a medium‐ and low‐secure forensic service	16
Provision of and trust in COVID‐19 vaccines information: Perspectives of people who have had COVID‐19	16
Children's behavioural and emotional reactions towards living with congenital heart disease in Saudi Arabia: A grounded theory study	16
Involving People With Lived Experience in Electronic Health Record Database Studies Reflections and Learning From the CHOOSE Study	16
The influence of social relationships and activities on the health of adults with obesity: A qualitative study	15
It takes three to tango: An ethnography of triadic involvement of residents, families and nurses in long‐term dementia care	15
Participant and caregiver perspectives on health feedback from a healthy lifestyle check	15
Reply to: Amplifying Women's Voices in Menopause Research: The Importance of Inclusive Perspectives [Letter]	15
Erratum to “Recruitment and Retention of Adolescents for an Ecological Momentary Assessment Measurement Burst Mental Health Study: The MHIM Engagement Strategy”	15
Comparative analysis of centrally mediated and inflammatory pain experiences amongst patients diagnosed with rheumatoid arthritis: A multimethods study	15
Epidermolysis Bullosa in Spain: A Qualitative Analysis of Its Social Impact on Families With Diagnosed Minors	15
Mitigating unintended consequences of co‐design in health care	15
Issue Information	15
Stakeholder Consultation to Establish Research Priorities for Specialist Dementia Nursing in the United Kingdom	14
How to make mental health services more youth‐friendly? A Delphi study involving young adults, parents and professionals	14
Alignment of patient‐centredness definitions with real‐life patient and clinician experiences: A qualitative study	14
Patient partners’ perspectives of meaningful engagement in synthesis reviews: A patient‐oriented rapid review	14
Identifying local barriers to access to healthcare services in Chile using a communitarian approach	14
Patient participation during primary health‐care encounters among adult patients with multimorbidity: A cross‐sectional study	14
A decision aid to support family carers of people living with dementia towards the end‐of‐life: Coproduction process, outcome and reflections	14
Barriers and facilitators to engaging with a digital self‐management programme for painful distal upper limb musculoskeletal disorders: A qualitative exploratory study	14
Codesigning a patient support portal with health professionals and men with prostate cancer: An action research study	14
Person‐centred sexual and reproductive health: A call for standardized measurement	14
Implementing and Delivering Culturally Centred Pharmacy Services Tailored to Ethnically Minoritised Populations: A Qualitative Systematic Review and Meta‐Ethnography	14
Involvement of adolescent representatives and coresearchers in mental health research: Experiences from a research project	14
Evaluating the role and effectiveness of co‐produced community‐based mental health interventions that aim to reduce suicide among adults: A systematic review	14
How Has ‘What Matters to You’ Been Used for Patient Care? A Scoping Review	13
The ultimate question? Evaluating the use of Net Promoter Score in healthcare: A systematic review	13
Research on the factors that influence patients with colorectal cancer participating in the prevention and control of surgical site infection: Based on the extended theory of planned behaviour	13
Long COVID and Health Inequalities: What's Next for Research and Policy Advocacy?	13
Codesigning person‐centred quality indicators with diverse communities: A qualitative patient engagement study	13
Challenges and Facilitators to Patient and Public Involvement In Stroke Research: Protocol for a Qualitative Study	13
Development and content validity of the Experienced Patient‐Centeredness Questionnaire (EPAT)—A best practice example for generating patient‐reported measures from qualitative data	13
Co‐Design of an Ecosystem of Services to Support Veteran Well‐Being and Reduce Excessive Alcohol Consumption	13
Centredness in health care: A systematic overview of reviews	13
A systematic review of theories, models and frameworks used for youth engagement in health research	13
The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases	12
Sleep hygiene behaviours mediate the association between health/e‐health literacy and mental wellbeing	12
Adapting a conceptual framework to engage diverse stakeholders in genomic/precision medicine research	12
Ecologising Invited and Uninvited Patient Participation in Russia	12
A rapid review of interventions to improve medicine self‐management for older people living at home	12
‘Including us, talking to us and creating a safe environment’—Youth patient and public involvement and the Walking In ScHools (WISH) Study: Lessons learned	12
Community health worker outreach to farmworkers in rural North Carolina: Learning from adaptations to the SARS‐CoV‐2 pandemic	12
An Interactive Vision‐Based 3D Augmented Reality System for In‐Home Physical Rehabilitation: A Qualitative Inquiry to Inform System Development	12
Structuring healthcare advance directives: Evidence from Chinese end‐of‐life cancer patients' treatment preferences	12
Compound impact of cognitive and physical decline: A qualitative interview study of people with Parkinson's and cognitive impairment, caregivers and professionals	12
Social determinants of health and long‐term conditions in people of Black African and Black Caribbean ethnicity living with HIV in London: A qualitative study	12
Using focus groups to inform a peer health navigator service for people who are transgender and gender diverse in Saskatchewan, Canada	12
Barriers to and enablers of the promotion of patient and family participation in primary healthcare nursing in Brazil, Germany and Spain: A qualitative study	11
A Patient and Public Engagement Project to Inform Dementia Care in a UK Hospital Trust	11
Issue Information	11
How do consumers respond when presented with novel doctor performance information? A multivariate regression analysis	11
Co‐Design of a Facilitated Self‐Management Toolkit for People With Parkinson's Disease	11
Tackling Inequalities in Access to Medicines for People Experiencing Homelessness: A Meta‐Ethnography and Qualitative Systematic Review	11
Experiences of patients with heart failure with medicines at transition intervention: Findings from the process evaluation of the Improving the Safety and Continuity of Medicines management at Transit	11
Patient preferences and choices as a reflection of trust—A cluster analysis comparing postsurgical perceptions in a private and a public hospital	11
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Design details for overdose education and take‐home naloxone kits: Codesign with family medicine, emergency department, addictions medicine and community	11
Ethical issues experienced by persons with rheumatoid arthritis in a wearable‐enabled physical activity intervention study	11
Trends in the psychosocial and mental health of HIV‐positive women in China from 2015 to 2020: Results from two cross‐sectional surveys	11
The Safe Environment for Every Kid Model in the Swedish Child Health Services: Adoption and Introduction in a Healthcare Region	11
The healthcare needs and general practice utilization of people with acquired neurological disability and complex needs: A scoping review	11
Partnering with older people as peer researchers	11
Evaluation of the Patient Innovation Partner Role: Perceived Benefits, Structures, Supports, and Recommendations for Lived Experience Engagement in Healthcare Innovation Teams	10
Involving Knowledge Users in Health Services Research: Collective Reflections and Learning From a National Evaluation of Recurrent Miscarriage Services	10
Translation and Validation of the Medication Understanding and Use Self‐Efficacy Scale Among Patients With Type 2 Diabetes in Taiwan	10
Implementing peer support work in mental health care in Germany: The methodological framework of the collaborative, participatory, mixed‐methods study (ImpPeer‐Psy5)	10
Epistemic justice in public involvement and engagement: Creating conditions for impact	10
Ensuring patient and public involvement in the transition to AI‐assisted mental health care: A systematic scoping review and agenda for design justice	10
A Mixed Methods Evaluation of the Statutory Duty of Candour in Victorian Health Services: Study Protocol	10
‘There's Nothing Wrong With You; You Just Need to Lose Weight’—A Qualitative Exploration of Pelvic Floor Dysfunction Among Women With Multiple Sclerosis and Their Interaction in Seeking Pelvic Healthc	10
Increasing Youth Peer Workers' Impact Through Integration: Peer Worker Perspectives on Best Practice in Youth Mental Health	10
Translation and Psychometric Evaluation in Cancer Care of the German Version of collaboRATETM—a 3‐item Patient‐reported Measure of Shared Decision‐Making	10
Effects of a shared decision‐making implementation programme on patient‐centred communication in oncology—Secondary analysis of a randomised controlled trial	10
Employing cofacilitation to balance power and priorities during health service codesign	10

Erratum to “What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability”	10
Coproducing an Ecological Momentary Assessment Measurement Burst Mental Health Study With Young People: The MHIM Coproduction Protocol	10
Co‐Authoring and Reporting on Lived Experience Engagement in Mental Health and/or Substance Research: A Qualitative Study and Guidance Document	10
More than a feeling? What does compassion in healthcare ‘look like’ to patients?	10
Multimodal Analysis of Stories Told by Mental Health Influencers on TikTok	10
Establishing Effective Patient Engagement Through a Terms of Reference to Foster Inclusivity and Empowerment in Research: Example From a Healthcare Transition Quality Indicators Project	9
Understanding the Preferences and Considerations of the Public Towards Risk‐Stratified Screening for Colorectal Cancer: Insights From Think‐Aloud Interviews Based on a Discrete Choice Experiment	9
Causes, Solutions and Health Inequalities: Comparing Perspectives of Professional Stakeholders and Community Participants Experiencing Low Income and Poor Health in London	9
Creating opportunities for patient participation in managing medications across transitions of care through formal and informal modes of communication	9
Adapting a codesign process with young people to prioritize outcomes for a systematic review of interventions to prevent self‐harm and suicide	9
User involvement in the making: Positions and types of knowledge enacted in the interaction between service users and researchers in user panel meetings	9
The importance of personal documentation for patients living with long‐term illness symptoms after pituitary surgery: A Constructivist Grounded Theory study	9
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	9
Experiences, perceptions and expectations of health services amongst marginalized populations in urban Australia: A meta‐ethnographic review of the literature	9
Issue Information	9
Patient versus physician preferences for lipid‐lowering drug therapy: A discrete choice experiment	9
Issue Information	9
The Acceptability, Safety and Impact of a Play Co‐Developed With Public Contributors as a Format for Disseminating Research on a Sensitive Subject	9
Optimizing the design and implementation of question prompt lists to support person‐centred care: A scoping review	9
Effectiveness of a structured short intervention against stigmatisation in chronic visible skin diseases: Results of a controlled trial in future educators	9
Widening or narrowing inequalities? The equity implications of digital tools to support COVID‐19 contact tracing: A qualitative study	9
Co‐designing resources to support older people with intellectual disabilities and their families plan for parental death and transitions in care	9
Factors affecting patients' journey with primary healthcare services during mental health‐related sick leave	9
Tools to evaluate medication management for caregivers of people living with dementia: A systematic review	9
How Do We Get the Public Into Public Health Research? Learnings and Key Recommendations From Initiating a Community Involvement Project Scheme	9
Recommendations for community pharmacy to improve access to medication advice for people from ethnic minority communities: A qualitative person‐centred codesign study	9
(Re)constructing identity following acquired brain injury: The complex journey of recovery after stroke	9
Corrigendum	9
Factors Influencing Kidney Transplantation Experiences for Patients From Culturally and Linguistically Diverse Backgrounds: A Qualitative Study	9
Behind the Screen: An Exploratory Study of Factors Influencing Breast Screening Uptake in Lancashire (UK)	9
Women's experiences along the ovarian cancer diagnostic pathway in Catalonia: A qualitative study	9
‘When a patient chooses to die at home, that's what they want… comfort, home’: Brilliance in community‐based palliative care nursing	9
Patients as partners in health research: A scoping review	9
Overarching Priorities for Health and Care Research in the United Kingdom: A Coproduced Synthesis of James Lind Alliance ‘Top 10s’	9
Patients' and Therapists' Views of Integrated Online CBT for Depression	9
Eliciting preferences for continuing medication among adult patients and parents of children with attention‐deficit hyperactivity disorder	9
Ten Priorities for Research Addressing the Intersections of Brain Injury, Mental Health and Addictions: A Stakeholder‐Driven Priority‐Setting Study	9
What Do We Know About Sharing Power in Co‐Production in Mental Health Research? A Systematic Review and Thematic Synthesis	9
The Bidirectional Engagement and Equity (BEE) Research Framework to Guide Community–Academic Partnerships: Developed From a Narrative Review and Diverse Stakeholder Perspectives	9
Frameworks Used to Engage Postsecondary Students in Campus Mental Health Research: A Scoping Review	8
Pragmatism as a paradigm for patient‐oriented research	8
Developing the Resident Measure of Safety in Care Homes (RMOS): A Delphi and Think Aloud Study	8
Using financial incentives to support service engagement of adults experiencing homelessness and mental illness: A qualitative analysis of key stakeholder perspectives	8
Co‐ideation and co‐design in co‐creation research: Reflections from the ‘Co‐Creating Safe Spaces’ project	8
Co‐building a training programme to facilitate patient, family and community partnership on research grants: A patient‐oriented research project	8
Reimagining consumer involvement: Resilient system indicators in the COVID‐19 pandemic response in New South Wales, Australia	8
The psychological consequences of living with coronary heart disease: Are patients' psychological needs served? A mixed‐method study in Germany	8
What really is nontokenistic fully inclusive patient and public involvement/engagement in research?	8
Engagement With Professional Stakeholders in Healthcare Research—The Case of the Dementia PersonAlised Care Team (D‐PACT) Project in the United Kingdom	8
How Do Australians Manage Diagnostic Testing Risks? Focus Groups Linked to a Model of Behaviour Change	8
Exploring the experiences and preferences of South Asian patients' of primary care in England since COVID‐19	8
Improving primary health care quality for refugees and asylum seekers: A systematic review of interventional approaches	8
Recommendations for a Communication Strategy to Support Informed Decision‐Making About Self or Clinician Sampling for Cervical Screening in the UK: Qualitative Study	8
Family caregiver roles and challenges in assisting patients with cancer treatment decision‐making: Analysis of data from a national survey	8
Exploring the barriers and facilitators to volunteering as an intervention for those with long‐term neurological conditions: How make therapeutic volunteering possible?	8
Towards understanding and improving medication safety for patients with mental illness in primary care: A multimethod study	8
Perceptions of the Impact of Comorbidity on the Bowel Cancer Screening Programme: Qualitative Study With Bowel Screening Participants and Staff	8
‘They Were Talking to Each Other but Not to Me’: Examining the Drivers of Patients' Poor Experiences During the Transition From the Hospital to Skilled Nursing Facility	8
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	8
Conceptual and practical challenges associated with understanding patient safety within community‐based mental health services	8
Engaging with Culturally and Linguistically Diverse Communities to Promote Palliative Care That Exceeds Expectation	8
A co‐created multimethod evaluation of recovery education in Ireland	8
Issue Information	8
Comparing an in‐person workshop and a postal Delphi survey for involving health service users in health care and health research prioritization	8
Defining Health Movements and Health Needs Across the Life Course: A Qualitative Study	8
A qualitative exploration of the barriers and facilitators affecting ethnic minority patient groups when accessing medicine review services: Perspectives of healthcare professionals	8
Item development for a patient‐reported measure of compassionate healthcare in action	8
Older Adults' Experiences and Expectations of Doctor–Patient Interactions During Early Hospital Care	8
Development and validation of educational multimedia to promote public health literacy about healthy cognitive aging	8
Prioritizing Chinese medicine clinical research questions in cancer palliative care from patient and caregiver perspectives	8
How to Approach a Child About Concerns for Their Mental Health and Seeking Help: A Delphi Expert Consensus Study to Develop Guidelines on Mental Health First Aid for Supporting Children	8
What do parents think about the quality and safety of care provided by hospitals to children and young people with an intellectual disability? A qualitative study using thematic analysis	8
Erratum	8
Balancing feeling ‘prepared’ without feeling ‘devoured’: A qualitative study of self‐care from the perspective of self‐empowered persons living with Parkinson's disease in Sweden	8
Nothing about us without us: A co‐production strategy for communities, researchers and stakeholders to identify ways of improving health and reducing inequalities	7
The perceptions of general practice among Central and Eastern Europeans in the United Kingdom: A systematic scoping review	7
‘I Do It All Alone’: The Burdens and Benefits of Being Diagnosed With, and Treated for, Colorectal Cancer During the Covid‐19 Pandemic	7
The process of co‐designing a model of social prescribing: An Australian case study	7
Assessing patient information needs for new antidiabetic medications to inform shared decision‐making: A best–worst scaling experiment in China	7
Assessing people with dementia participating in cognitive stimulation activities—A qualitative pilot video analysis exploring the importance of facilitating the participation	7
The meaning of the recovery process and its stages for people attending a mental health day hospital: 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
Assessment of medication adherence, medication safety awareness and medication practice among patients with lung cancer: A multicentre cross‐sectional study	7
Patients' experiences of, and engagement with, remote home monitoring services for COVID‐19 patients: A rapid mixed‐methods study	7
Implementing public involvement throughout the research process—Experience and learning from the GPs in EDs study	7
Consumers' Contribution to Health Research: Australian Research Organisations' Perspectives	7
Exploring adolescents' experiences of continuing to wear face masks during COVID‐19: A qualitative descriptive study in Barcelona (Spain)	7
Parenting through place‐of‐care disruptions: A qualitative study of parents' experiences of neonatal care	7
Investigating the Factors Behind Patients' Desire and Decision to be Accompanied: A Cross‐Sectional Analysis	7
Expectations of a new opt‐out system of consent for deceased organ donation in England: A qualitative interview study	7
Accompanying patients in clinical oncology teams: Reported activities and perceived effects	7
Transitional care decision‐making through the eyes of older people and informal caregivers: An in‐depth interview‐based study	7
Patient perceptions of in‐hospital laboratory blood testing: A patient‐oriented and patient co‐designed qualitative study	7
Using World Cafés to engage an Australian culturally and linguistically diverse community around human papillomavirus vaccination	7
An umbrella review of reviews on challenges to meaningful adolescent involvement in health research	7