Health Expectations

Article	Citations
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	169
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	124
Feasibility of a best–worst scaling exercise to set priorities for autism research	96
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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	82
Continuity Is Essential: The Experiences of Co‐Design Participants During the Implementation of a New Health Service	81
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	68
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	64
Indicators for adequate diabetes care for the indigenous communities of Ecuador	62
Children's Communication Choices About Musculoskeletal Pain and Injury: Insights From a Public Involvement Event	52
Identifying Common Patient‐Oriented Priorities for Child and Adolescent Health Research and Care: A Systematic Review of Priority Setting Partnerships	47
Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey	46
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice	43
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	40
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers	40
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	39
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	38
Inside Front Cover: Volume 25 Issue 1	35
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	35
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	34
Youth engagement in mental health research: A systematic review	33
Participatory research with carers: A systematic review and narrative synthesis	33
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	32
Ripple Effects Mapping: Evaluating Multilevel Perspectives and Impacts of a Statewide Community–Academic Partnership Network on Covid‐19 Health Disparities	31
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	30

Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	30
Just a story? Leadership, lived experience and integrated care	30
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	29
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	29
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	28
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	27
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	27
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	27
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	26
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs	25
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	25
Patient preferences for heart valve disease intervention	25
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	25
Agenda Setting in Outpatient Consultation of Older Adults With Long‐COVID	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
Uncovering the Dynamic System Driving Older Adults' Vitality: A Causal Loop Diagram Co‐Created With Dutch Older Adults	24
Perceptions and Significance of Long Covid Diagnoses From the Perspectives of Children and Young People With Long Covid, Their Parents and Professionals	23
Illness Expectations and Asthma Symptoms: A 6‐Month Longitudinal Study	23
‘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	23
HIV Care Seeking Pathways and Barriers to the Continuum of Care Faced by Persons Living With HIV in Rural Nepal: A Qualitative Study	22
‘They need to ask me first’. Community engagement with low‐income citizens. A realist qualitative case‐study	21
Developing an Inclusive Dance Guide for Children With Cerebral Palsy: A Co‐Design Process and Initial Feasibility Study	21
‘Lifts your spirits, lifts your mind’: A co‐produced mixed‐methods exploration of the benefits of green and blue spaces for mental wellbeing	21
Knowledge Families Hold: Co‐Production and Co‐Research With Mental Health Family Carers in Understanding Experiences During the COVID‐19 Pandemic	21
The Challenging Process of Developing an Antenatal Social Intervention for Parents From Culturally Diverse Backgrounds to Reduce Postnatal Distress: A Participatory Action Research Study	21
Self‐directed self‐management interventions to prevent or address distress in young people with long‐term physical conditions: A rapid review	20
Viewpoints among experts and the public in the Netherlands on including a lifestyle criterion in the healthcare priority setting	20
Needs assessment for health service design for people with back pain in a hospital setting: A qualitative study	20
The interactive dimensions of encounters in HIV care: From trauma to relational traumatic growth	19
Partnering With Patients to Conduct High‐Quality Research – Where Have We Been and Where Are We Going?	19
How we define recurrent miscarriage matters: A qualitative exploration of the views of people with professional or lived experience	19
Behaviour, barriers and facilitators of shared decision making in breast cancer surgical treatment: A qualitative systematic review using a ‘Best Fit’ framework approach	19
Evaluation of aspiration risk by relatives of inpatients in the neurology service: A metaphor analysis	19
Physical Health Checks and Follow‐Up Care in Deprived and Ethnically Diverse People With Severe Mental Illness: Co‐Designed Recommendations for Better Care	19
Delivery of supported self‐management in remote asthma reviews: A systematic rapid realist review	18
Content validity testing of the INTERMED Self‐Assessment in a sample of adults with rheumatoid arthritis and rheumatology healthcare providers	18
Assessing the environment for engagement in health services: The Audit for Consumer Engagement (ACE) tool	18
‘Physical well‐being is our top priority’: Healthcare professionals' challenges in supporting psychosocial well‐being in stroke services	17
‘But … Would I Be Able to Toast With Friends?’ When Service Users Ask for New Care Pathways	17
Person‐centred caregiver singing for people living with dementia in South Africa: A mixed methods evaluation of acceptability, feasibility, and professional caregivers' experiences	17
Exploring the lived experience of receiving mental health crisis care at emergency departments, crisis phone lines and crisis care alternatives	17
Hospital Food Service Experiences Between Older Patients From English‐ and Non‐English Speaking Backgrounds in a Large Public Hospital in Australia: A Qualitative Analysis	17
Patient and Staff Insights on Digital Care Pathways for Patients With Low Back Pain in the Emergency Department: A Qualitative Study	17
Experiences and expectations of receiving volunteer services among home‐based elderly in Chinese urban areas: A qualitative study	17
The experiences of psychiatric patients, their caregivers and companions in upholding patient dignity during hospitalization: A qualitative study	17
Reflections on the opportunities and challenges of applying experience‐based co‐design (EBCD) to phase 1 clinical trials in oncology	17
All Good Without Anything Good. Beyond Survival: Understanding the Psychosocial Experiences of Individuals With Chronic Kidney Disease and Their Caregivers in Sri Lanka	17
Participatory approaches for developing a practical handbook integrating health information for supporting individuals with mild cognitive impairment and their families	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
Announcements of Death During the COVID‐19 Pandemic: A Qualitative Study of Family Experiences	16

Children's behavioural and emotional reactions towards living with congenital heart disease in Saudi Arabia: A grounded theory study	16
Family Interviews Improve Health Service Recommendations in Mortality Review Process: A Mixed‐Methods Assessment	16
Co‐Creation in Research: Further Reflections From the ‘Co‐Creating Safe Spaces’ Project	16
Problem‐based shared decision making: The role of canonical SDM steps	16
Consumer Experience of an Australian Multidisciplinary Long COVID Clinic That Incorporates Personalised Exercise Prescription: A Qualitative Analysis	15
Provision of and trust in COVID‐19 vaccines information: Perspectives of people who have had COVID‐19	15
The HUSH Project: Using codesign to reduce sleep disruptions for patients in hospital	15
The influence of social relationships and activities on the health of adults with obesity: A qualitative study	15
Involving People With Lived Experience in Electronic Health Record Database Studies Reflections and Learning From the CHOOSE Study	15
Experiences and Perceptions of Self‐Harm in Rural‐Dwelling Adults: A Rapid Review of Qualitative Evidence	15
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	15
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	15
Development of person‐centred quality indicators for aged care assessment services in Australia: A mixed methods study	15
Women's experiences of care after stillbirth and obstetric fistula: A phenomenological study in Kenya	15
Patient perspectives on primary care for multimorbidity: An integrative review	14
Gender bias in shared decision‐making among cancer care guidelines: A systematic review	14
Issue Information	14
Person‐centred sexual and reproductive health: A call for standardized measurement	14
Developing a Women's Thought Collective methodology for health research: The roles and responsibilities of researchers in the reflexive co‐production of knowledge	14
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	14
Identifying local barriers to access to healthcare services in Chile using a communitarian approach	14
Understanding the cultural environment of the outpatient care setting for patients with dementia receiving cancer treatment: A qualitative study	14
Reply to: Amplifying Women's Voices in Menopause Research: The Importance of Inclusive Perspectives [Letter]	14
Exploring Patient Understandings of Navigation Services Within Alberta's Healthcare System: A Qualitative Study	14
Erratum to “Recruitment and Retention of Adolescents for an Ecological Momentary Assessment Measurement Burst Mental Health Study: The MHIM Engagement Strategy”	13
Long COVID and Health Inequalities: What's Next for Research and Policy Advocacy?	13
A Proposal for Addressing Bioethical Concerns Along the 10‐Step Framework for Community Engagement	13
Codesigning a patient support portal with health professionals and men with prostate cancer: An action research study	13
Centredness in health care: A systematic overview of reviews	13
How to make mental health services more youth‐friendly? A Delphi study involving young adults, parents and professionals	13
Alignment of patient‐centredness definitions with real‐life patient and clinician experiences: A qualitative study	13
Challenges and Facilitators to Patient and Public Involvement In Stroke Research: Protocol for a Qualitative Study	12
Participant and caregiver perspectives on health feedback from a healthy lifestyle check	12
Epidermolysis Bullosa in Spain: A Qualitative Analysis of Its Social Impact on Families With Diagnosed Minors	12
Implementing and Delivering Culturally Centred Pharmacy Services Tailored to Ethnically Minoritised Populations: A Qualitative Systematic Review and Meta‐Ethnography	12
Development and content validity of the Experienced Patient‐Centeredness Questionnaire (EPAT)—A best practice example for generating patient‐reported measures from qualitative data	12
Stakeholder Consultation to Establish Research Priorities for Specialist Dementia Nursing in the United Kingdom	12
How Has ‘What Matters to You’ Been Used for Patient Care? A Scoping Review	12
Exiting Surveillance From Abdominal Aortic Aneurysm Screening: The Views of Clinicians, and Men in Surveillance and Their Family Members	12
Barriers to Care for Adults With Sickle Cell Disease: A Qualitative Descriptive Study	12
Involvement of adolescent representatives and coresearchers in mental health research: Experiences from a research project	12
Co‐Design of an Ecosystem of Services to Support Veteran Well‐Being and Reduce Excessive Alcohol Consumption	12
Comparative analysis of centrally mediated and inflammatory pain experiences amongst patients diagnosed with rheumatoid arthritis: A multimethods study	12
Recognising Consumers' Contributions to Health Research: Co‐Designing a Remuneration Framework for the Australian Context	12
Including Prisoners in Research Design: Codevelopment of a Practical Guidance Toolkit to Support Intervention Delivery to Address the Physical and Mental Health of Older Prisoners (PAMHOP) Study	12
The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases	12
Evaluating the role and effectiveness of co‐produced community‐based mental health interventions that aim to reduce suicide among adults: A systematic review	12
Barriers and facilitators to engaging with a digital self‐management programme for painful distal upper limb musculoskeletal disorders: A qualitative exploratory study	12
Codesigning person‐centred quality indicators with diverse communities: A qualitative patient engagement study	12
Translation and Validation of the Medication Understanding and Use Self‐Efficacy Scale Among Patients With Type 2 Diabetes in Taiwan	11
Coproducing an Ecological Momentary Assessment Measurement Burst Mental Health Study With Young People: The MHIM Coproduction Protocol	11
Adapting a codesign process with young people to prioritize outcomes for a systematic review of interventions to prevent self‐harm and suicide	11
How do consumers respond when presented with novel doctor performance information? A multivariate regression analysis	11
Ecologising Invited and Uninvited Patient Participation in Russia	11
A systematic review of theories, models and frameworks used for youth engagement in health research	11
Issue Information	11
Structuring healthcare advance directives: Evidence from Chinese end‐of‐life cancer patients' treatment preferences	11
Design details for overdose education and take‐home naloxone kits: Codesign with family medicine, emergency department, addictions medicine and community	11
A Patient and Public Engagement Project to Inform Dementia Care in a UK Hospital Trust	11
An Interactive Vision‐Based 3D Augmented Reality System for In‐Home Physical Rehabilitation: A Qualitative Inquiry to Inform System Development	11
Employing cofacilitation to balance power and priorities during health service codesign	11
Multimodal Analysis of Stories Told by Mental Health Influencers on TikTok	11
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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 ultimate question? Evaluating the use of Net Promoter Score in healthcare: A systematic review	11
The Safe Environment for Every Kid Model in the Swedish Child Health Services: Adoption and Introduction in a Healthcare Region	11
Evaluation of the Patient Innovation Partner Role: Perceived Benefits, Structures, Supports, and Recommendations for Lived Experience Engagement in Healthcare Innovation Teams	11
Using focus groups to inform a peer health navigator service for people who are transgender and gender diverse in Saskatchewan, Canada	11
Community health worker outreach to farmworkers in rural North Carolina: Learning from adaptations to the SARS‐CoV‐2 pandemic	11
Tackling Inequalities in Access to Medicines for People Experiencing Homelessness: A Meta‐Ethnography and Qualitative Systematic Review	11
Erratum to “What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability”	11
Sleep hygiene behaviours mediate the association between health/e‐health literacy and mental wellbeing	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
Increasing Youth Peer Workers' Impact Through Integration: Peer Worker Perspectives on Best Practice in Youth Mental Health	11
A Mixed Methods Evaluation of the Statutory Duty of Candour in Victorian Health Services: Study Protocol	11
Involving Knowledge Users in Health Services Research: Collective Reflections and Learning From a National Evaluation of Recurrent Miscarriage Services	11
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	10
Experiences, perceptions and expectations of health services amongst marginalized populations in urban Australia: A meta‐ethnographic review of the literature	10
‘When a patient chooses to die at home, that's what they want… comfort, home’: Brilliance in community‐based palliative care nursing	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

Implementing peer support work in mental health care in Germany: The methodological framework of the collaborative, participatory, mixed‐methods study (ImpPeer‐Psy5)	10
Ethical issues experienced by persons with rheumatoid arthritis in a wearable‐enabled physical activity intervention study	10
Epistemic justice in public involvement and engagement: Creating conditions for impact	10
Patient preferences and choices as a reflection of trust—A cluster analysis comparing postsurgical perceptions in a private and a public hospital	10
Stakeholder Perspectives on Built Environmental Factors to Support Stroke Rehabilitation and Return to Everyday Life	10
Issue Information	10
A rapid review of interventions to improve medicine self‐management for older people living at home	10
‘Including us, talking to us and creating a safe environment’—Youth patient and public involvement and the Walking In ScHools (WISH) Study: Lessons learned	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
Co‐Design of a Facilitated Self‐Management Toolkit for People With Parkinson's Disease	10
Barriers to and enablers of the promotion of patient and family participation in primary healthcare nursing in Brazil, Germany and Spain: A qualitative study	10
Compound impact of cognitive and physical decline: A qualitative interview study of people with Parkinson's and cognitive impairment, caregivers and professionals	10
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	10
Recommendations for a Communication Strategy to Support Informed Decision‐Making About Self or Clinician Sampling for Cervical Screening in the UK: Qualitative Study	10
Corrigendum	10
Co‐Authoring and Reporting on Lived Experience Engagement in Mental Health and/or Substance Research: A Qualitative Study and Guidance Document	10
Effects of a shared decision‐making implementation programme on patient‐centred communication in oncology—Secondary analysis of a randomised controlled trial	10
Adapting a conceptual framework to engage diverse stakeholders in genomic/precision medicine research	10
The healthcare needs and general practice utilization of people with acquired neurological disability and complex needs: A scoping review	10
More than a feeling? What does compassion in healthcare ‘look like’ to patients?	10
Co‐designing resources to support older people with intellectual disabilities and their families plan for parental death and transitions in care	10
Patient versus physician preferences for lipid‐lowering drug therapy: A discrete choice experiment	9
Comparing an in‐person workshop and a postal Delphi survey for involving health service users in health care and health research prioritization	9
Patients' and Therapists' Views of Integrated Online CBT for Depression	9
Creating opportunities for patient participation in managing medications across transitions of care through formal and informal modes of communication	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
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
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
Listening to Women's Voices: A Patient and Public Involvement Exercise Exploring Vulval Reconstructive Surgery for UK Women With Female Genital Mutilation (FGM)	9
Issue Information	9
User Input in the Development of Digital Sexual Health Tools: A Scoping Review and Guidance for Tool Developers	9
Family caregiver roles and challenges in assisting patients with cancer treatment decision‐making: Analysis of data from a national survey	9
(Re)constructing identity following acquired brain injury: The complex journey of recovery after stroke	9
Factors Influencing Kidney Transplantation Experiences for Patients From Culturally and Linguistically Diverse Backgrounds: A Qualitative Study	9
Optimizing the design and implementation of question prompt lists to support person‐centred care: A scoping review	9
Causes, Solutions and Health Inequalities: Comparing Perspectives of Professional Stakeholders and Community Participants Experiencing Low Income and Poor Health in London	9
Defining Health Movements and Health Needs Across the Life Course: A Qualitative Study	9
Factors affecting patients' journey with primary healthcare services during mental health‐related sick leave	9
Co‐Creation Methodology for Developing a Racial Inclusivity Training Resource in Physiotherapy Education	9
Ten Priorities for Research Addressing the Intersections of Brain Injury, Mental Health and Addictions: A Stakeholder‐Driven Priority‐Setting Study	9
How Do We Get the Public Into Public Health Research? Learnings and Key Recommendations From Initiating a Community Involvement Project Scheme	9
Eliciting preferences for continuing medication among adult patients and parents of children with attention‐deficit hyperactivity disorder	9
Challenges of Inclusion: A Population‐Based Interview Study of Long Covid	9
Behind the Screen: An Exploratory Study of Factors Influencing Breast Screening Uptake in Lancashire (UK)	9
Recommendations for community pharmacy to improve access to medication advice for people from ethnic minority communities: A qualitative person‐centred codesign study	9
The importance of personal documentation for patients living with long‐term illness symptoms after pituitary surgery: A Constructivist Grounded Theory study	9
Frameworks Used to Engage Postsecondary Students in Campus Mental 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
Exploring the barriers and facilitators to volunteering as an intervention for those with long‐term neurological conditions: How make therapeutic volunteering possible?	8
Reimagining consumer involvement: Resilient system indicators in the COVID‐19 pandemic response in New South Wales, Australia	8
Women's experiences along the ovarian cancer diagnostic pathway in Catalonia: A qualitative study	8
What Do We Know About Sharing Power in Co‐Production in Mental Health Research? A Systematic Review and Thematic Synthesis	8
Erratum	8
A qualitative evaluation of a co‐design process involving young people at risk of suicide	8
Correction to “Creating Safer Cancer Care With Ethnic Minority Patients: A Qualitative Analysis of the Experiences of Cancer Service Staff”	8
Co‐Designing an Engagement Strategy to Include the Voices of a Minority Group in Assessing the Quality of Maternity and Neonatal Care	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
Perceptions of the Impact of Comorbidity on the Bowel Cancer Screening Programme: Qualitative Study With Bowel Screening Participants and Staff	8
Co‐building a training programme to facilitate patient, family and community partnership on research grants: A patient‐oriented research project	8
Developing the Resident Measure of Safety in Care Homes (RMOS): A Delphi and Think Aloud Study	8
Exploring the experiences and preferences of South Asian patients' of primary care in England since COVID‐19	8
Pragmatism as a paradigm for patient‐oriented research	8
Widening or narrowing inequalities? The equity implications of digital tools to support COVID‐19 contact tracing: A qualitative study	8
Improving primary health care quality for refugees and asylum seekers: A systematic review of interventional approaches	8
Co‐Design of a Framework for Person‐Centred Care at Emergency Department Triage and Waiting Room	8
How Do Australians Manage Diagnostic Testing Risks? Focus Groups Linked to a Model of Behaviour Change	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
Engaging with Culturally and Linguistically Diverse Communities to Promote Palliative Care That Exceeds Expectation	8
Item development for a patient‐reported measure of compassionate healthcare in action	8
A co‐created multimethod evaluation of recovery education in Ireland	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
The Bidirectional Engagement and Equity (BEE) Research Framework to Guide Community–Academic Partnerships: Developed From a Narrative Review and Diverse Stakeholder Perspectives	8
Using financial incentives to support service engagement of adults experiencing homelessness and mental illness: A qualitative analysis of key stakeholder perspectives	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
Engagement of People With Lived Experience in Spinal Cord Injury to Address Innovation Priorities	8
Older Adults' Experiences and Expectations of Doctor–Patient Interactions During Early Hospital Care	8
Engagement With Professional Stakeholders in Healthcare Research—The Case of the Dementia PersonAlised Care Team (D‐PACT) Project in the United Kingdom	8
Co‐ideation and co‐design in co‐creation research: Reflections from the ‘Co‐Creating Safe Spaces’ project	8
“The Culturally and Linguistically Diverse Community Is Not Just Minoritised But Ignored”: Engaging Culturally and Linguistically Diverse Communities in Australia With Blood‐Borne Viruses and Sexually	7
Using World Cafés to engage an Australian culturally and linguistically diverse community around human papillomavirus vaccination	7
A Novel Content and Usability Analysis of UK Professional Regulator Information About Raising a Concern by Members of the Public	7
Exploring adolescents' experiences of continuing to wear face masks during COVID‐19: A qualitative descriptive study in Barcelona (Spain)	7
Patterns of Health Services and Medicine Utilisation by First‐Generation Pakistani Immigrants in New Zealand	7
Developing a Set of Key Principles for Care Planning Within Older Adult Care Homes: A Modified Delphi Survey	7
Assessing the Gap Between Women's Expectations and Perceptions of the Quality of Intrapartum Care in Jordan: A Two‐Stage Study Using the SERVQUAL Model	7
Accompanying patients in clinical oncology teams: Reported activities and perceived effects	7
From polarity to plurality: Perceptions of COVID‐19 and policy measures in England and Scotland	7
Investigating the Factors Behind Patients' Desire and Decision to be Accompanied: A Cross‐Sectional Analysis	7
Response to Comments on “Designing a Positive Health Dialogue Tool for Adolescents and Young Adults: A Mixed Methods Study”	7
The perceptions of general practice among Central and Eastern Europeans in the United Kingdom: A systematic scoping review	7
Transitional care decision‐making through the eyes of older people and informal caregivers: An in‐depth interview‐based study	7
Four Years in, What Are the Research Priorities for Long COVID? A Research Priority‐Setting Partnership Between People With Lived Experience, Carers, Clinicians and Researchers	7
Time for a New Norm: Experiences of ‘Being Informed’ and ‘Having Choice’ for Prenatal Screening for Chromosomal Conditions: A Qualitative Study	7
Consumers' Contribution to Health Research: Australian Research Organisations' Perspectives	7
Issue Information	7