Health Expectations

Article	Citations
	134
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	120
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	117
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	113
Psychosocial Impact of Breast Density Notification Through Breast Cancer Screening: A Qualitative Interview Study	88
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	77
Participatory research with carers: A systematic review and narrative synthesis	77
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	73
Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey	68
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	62
Co‐Developing User‐Centred Nutrition Educational Resources to Integrate Nutrition Into Multiple Sclerosis Care: A Collaborative Approach With Healthcare Professionals and Healthcare Consumers	58
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	53
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	50
Ripple Effects Mapping: Evaluating Multilevel Perspectives and Impacts of a Statewide Community–Academic Partnership Network on Covid‐19 Health Disparities	47
From Co‐Design to Quality Improvement: Using the Double Diamond Framework to Develop Primary Care Redesign Priorities for Hypertension Care	45
Youth engagement in mental health research: A systematic review	42
Co‐Designing a Culturally Tailored Nutrition Resource With African Migrant Women and Healthcare Professionals in Australia	41
Co‐Design of a Community of Practice for People With Personal and Professional Expertise or Interest in Dementia in Australia	40
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	39
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	38
Just a story? Leadership, lived experience and integrated care	38
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	37
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	36
Look on the Bright Side: The Interactional Construction of a Survivor Identity in the Breast Cancer Clinic	36
Identifying Common Patient‐Oriented Priorities for Child and Adolescent Health Research and Care: A Systematic Review of Priority Setting Partnerships	36

Continuity Is Essential: The Experiences of Co‐Design Participants During the Implementation of a New Health Service	35
Identification and Applications of Key Elements in the Development of Pictorial Support for People With Aphasia After Stroke: A Co‐Design Approach	35
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	35
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	33
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	32
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	31
What Supports and Constrains the Implementation of Robust and Rapid Evaluation Within Local Government Public Health Systems?	29
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	28
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	27
Feasibility of a best–worst scaling exercise to set priorities for autism research	26
Children's Communication Choices About Musculoskeletal Pain and Injury: Insights From a Public Involvement Event	26
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers	25
Indicators for adequate diabetes care for the indigenous communities of Ecuador	25
Patient preferences for heart valve disease intervention	25
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice	25
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	24
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs	24
Agenda Setting in Outpatient Consultation of Older Adults With Long‐COVID	24
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	24
Uncovering the Dynamic System Driving Older Adults' Vitality: A Causal Loop Diagram Co‐Created With Dutch Older Adults	23
HIV Care Seeking Pathways and Barriers to the Continuum of Care Faced by Persons Living With HIV in Rural Nepal: A Qualitative Study	23
Evaluation of aspiration risk by relatives of inpatients in the neurology service: A metaphor analysis	23
Partnering With Patients to Conduct High‐Quality Research – Where Have We Been and Where Are We Going?	22
Counting the Cost: The Hidden Financial Realities of Neuromuscular Disease Through Patient and Family Perspectives	22
Hospital Food Service Experiences Between Older Patients From English‐ and Non‐English Speaking Backgrounds in a Large Public Hospital in Australia: A Qualitative Analysis	22
The Challenging Process of Developing an Antenatal Social Intervention for Parents From Culturally Diverse Backgrounds to Reduce Postnatal Distress: A Participatory Action Research Study	22
People With Non‐Communicable Diseases Using Ayurveda: A UK‐Based Qualitative Study	21
A Qualitative Evaluation Exploring Co‐Production of Falls Management in Care Homes	21
The experiences of psychiatric patients, their caregivers and companions in upholding patient dignity during hospitalization: A qualitative study	20
‘Lifts your spirits, lifts your mind’: A co‐produced mixed‐methods exploration of the benefits of green and blue spaces for mental wellbeing	20
The interactive dimensions of encounters in HIV care: From trauma to relational traumatic growth	20
Mobilising Knowledge for General Practice Decarbonisation: Maximising Impact Through a Multi‐Stakeholder Workshop	20
‘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	20
‘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	20
Behaviour, barriers and facilitators of shared decision making in breast cancer surgical treatment: A qualitative systematic review using a ‘Best Fit’ framework approach	19
Experiences and expectations of receiving volunteer services among home‐based elderly in Chinese urban areas: A qualitative study	19
All Good Without Anything Good. Beyond Survival: Understanding the Psychosocial Experiences of Individuals With Chronic Kidney Disease and Their Caregivers in Sri Lanka	19
Content validity testing of the INTERMED Self‐Assessment in a sample of adults with rheumatoid arthritis and rheumatology healthcare providers	19
Developing an Inclusive Dance Guide for Children With Cerebral Palsy: A Co‐Design Process and Initial Feasibility Study	19
Using Arts‐Based Methods to Involve People Living in Tower Hamlets With Multiple Long‐Term Conditions in the Development of Artificial Intelligence Tools in Healthcare Research	19
Announcements of Death During the COVID‐19 Pandemic: A Qualitative Study of Family Experiences	19
Perceptions and Significance of Long Covid Diagnoses From the Perspectives of Children and Young People With Long Covid, Their Parents and Professionals	19
Community Health Workers' and Pharmacists' Perspectives of a CHW‐Pharmacist Collaboration Model to Support Medication Adherence	19
Person‐centred caregiver singing for people living with dementia in South Africa: A mixed methods evaluation of acceptability, feasibility, and professional caregivers' experiences	18
Reflections on the opportunities and challenges of applying experience‐based co‐design (EBCD) to phase 1 clinical trials in oncology	18
Exploring the lived experience of receiving mental health crisis care at emergency departments, crisis phone lines and crisis care alternatives	18
‘But … Would I Be Able to Toast With Friends?’ When Service Users Ask for New Care Pathways	18
Knowledge Families Hold: Co‐Production and Co‐Research With Mental Health Family Carers in Understanding Experiences During the COVID‐19 Pandemic	18
Patient and Staff Insights on Digital Care Pathways for Patients With Low Back Pain in the Emergency Department: A Qualitative Study	18
Self‐directed self‐management interventions to prevent or address distress in young people with long‐term physical conditions: A rapid review	18

A Youth‐Led Evaluation of Adolescent Involvement in a Project on Development of Guidelines for Adolescent Involvement in Health Research	18
‘Physical well‐being is our top priority’: Healthcare professionals' challenges in supporting psychosocial well‐being in stroke services	18
How we define recurrent miscarriage matters: A qualitative exploration of the views of people with professional or lived experience	17
Illness Expectations and Asthma Symptoms: A 6‐Month Longitudinal Study	17
Assessing the environment for engagement in health services: The Audit for Consumer Engagement (ACE) tool	17
Contextualisation of the safeTALK™ Suicide Prevention Program: A Descriptive Qualitative Study	17
Physical Health Checks and Follow‐Up Care in Deprived and Ethnically Diverse People With Severe Mental Illness: Co‐Designed Recommendations for Better Care	17
Family Interviews Improve Health Service Recommendations in Mortality Review Process: A Mixed‐Methods Assessment	17
Co‐Creation in Research: Further Reflections From the ‘Co‐Creating Safe Spaces’ Project	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
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
Reply to: Amplifying Women's Voices in Menopause Research: The Importance of Inclusive Perspectives [Letter]	16
The HUSH Project: Using codesign to reduce sleep disruptions for patients in hospital	16
Women's experiences of care after stillbirth and obstetric fistula: A phenomenological study in Kenya	16
Children's behavioural and emotional reactions towards living with congenital heart disease in Saudi Arabia: A grounded theory study	16
Consumer Experience of an Australian Multidisciplinary Long COVID Clinic That Incorporates Personalised Exercise Prescription: A Qualitative Analysis	16
Provision of and trust in COVID‐19 vaccines information: Perspectives of people who have had COVID‐19	16
Public and Patient Involvement in Artificial Intelligence and Big Data Healthcare Research: An Exploration of Issues and Challenges Within the AI‐Multiply Project	16
Investigating the Applicability of the SAFER‐YCL Care Bundle for Transitions From CAMHS Crisis and Liaison Services: The Barriers and Enablers	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
Experiences and Perceptions of Self‐Harm in Rural‐Dwelling Adults: A Rapid Review of Qualitative Evidence	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	15
Involving People With Lived Experience in Electronic Health Record Database Studies Reflections and Learning From the CHOOSE Study	15
Development of person‐centred quality indicators for aged care assessment services in Australia: A mixed methods study	15
Cultural Adaptations of Healthcare Interventions: A Step‐by‐Step Guide	15
Patient perspectives on primary care for multimorbidity: An integrative review	15
Integrating Clinical Perspectives in the Prevention of Teenage Pregnancy	15
The influence of social relationships and activities on the health of adults with obesity: A qualitative study	15
Gender bias in shared decision‐making among cancer care guidelines: A systematic review	15
Problem‐based shared decision making: The role of canonical SDM steps	15
Perceptions of HIV‐Related Stigma Among Youth Exposed to the PPSAC Programme in Yaoundé, Cameroon	15
Researching Sensitive Topics: The Value of Inclusive Patient and Public Involvement and Engagement in the Design and Implementation of the Larger Bodies in Radiography Project	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
Prevalence of Hearing, Vision and Cognitive Impairment and Impact in Older Adults in Home Care: A Study Protocol	15
Engaging Culturally and Linguistically Diverse Communities to Prepare for Lung Cancer Screening Implementation in Australia: A Qualitative Focus Group Study	14
Co‐Designing Lived Experience Guide Support for First Responder Mental Health: Defining the Role and Considerations for Implementation	14
Implementing and Delivering Culturally Centred Pharmacy Services Tailored to Ethnically Minoritised Populations: A Qualitative Systematic Review and Meta‐Ethnography	14
Stakeholder Consultation to Establish Research Priorities for Specialist Dementia Nursing in the United Kingdom	14
Participant and caregiver perspectives on health feedback from a healthy lifestyle check	14
Understanding the cultural environment of the outpatient care setting for patients with dementia receiving cancer treatment: A qualitative study	14
Exploring Patient Understandings of Navigation Services Within Alberta's Healthcare System: A Qualitative Study	14
Co‐Design of an Ecosystem of Services to Support Veteran Well‐Being and Reduce Excessive Alcohol Consumption	14
Erratum to “Recruitment and Retention of Adolescents for an Ecological Momentary Assessment Measurement Burst Mental Health Study: The MHIM Engagement Strategy”	14
Issue Information	14
A Proposal for Addressing Bioethical Concerns Along the 10‐Step Framework for Community Engagement	14
How Has ‘What Matters to You’ Been Used for Patient Care? A Scoping Review	14
Comparative analysis of centrally mediated and inflammatory pain experiences amongst patients diagnosed with rheumatoid arthritis: A multimethods study	14
Integrating Community Health Workers Into Clinical Settings	13
Recognising Consumers' Contributions to Health Research: Co‐Designing a Remuneration Framework for the Australian Context	13
The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases	13
Long COVID and Health Inequalities: What's Next for Research and Policy Advocacy?	13
Telemedicine and Cultural Competency in Dementia Care: Mapping Stakeholder Roles in Digital Toolkit Development in SSA: A Systematic Review	13
A systematic review of theories, models and frameworks used for youth engagement in health research	13
‘It Was a Bit of a Now or Never Situation’: Experiences of Preconception Care and Support for Women With Multiple Long‐Term Health Conditions	13
Stories From Black Women in Iowa About Reproductive Health Care Experiences, Self‐Advocacy, and Recommendations for Change	13
Leveraging Community‐Based System Dynamics to Understand Long Covid Disparities in African American Communities: A Model for Health Equity Research	13
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	13
Challenges and Facilitators to Patient and Public Involvement In Stroke Research: Protocol for a Qualitative Study	13
Feasibility and Acceptability of an Incentive‐Based Intervention for Health Behaviour Change Among Rural Residents in China: A Mixed‐Methods Evaluation	13
Co‐Producing Personalised Discharge Planning: Developing a Toolkit to Improve Caregiver Involvement in Hospital Transitions	13
Living With Diabetes in Alberta: Patient and Caregiver Priorities for Diabetes Care, Management, and Treatment	13
Epidermolysis Bullosa in Spain: A Qualitative Analysis of Its Social Impact on Families With Diagnosed Minors	13
Alignment of patient‐centredness definitions with real‐life patient and clinician experiences: A qualitative study	13
Barriers to Care for Adults With Sickle Cell Disease: A Qualitative Descriptive Study	13
Progress Through Engagement: A Systematic Review and Thematic Synthesis of Qualitative Community‐Based Participatory Research in Vision Impairment	13
Exiting Surveillance From Abdominal Aortic Aneurysm Screening: The Views of Clinicians, and Men in Surveillance and Their Family Members	13
Translation and Validation of the Medication Understanding and Use Self‐Efficacy Scale Among Patients With Type 2 Diabetes in Taiwan	12
The ultimate question? Evaluating the use of Net Promoter Score in healthcare: A systematic review	12
Erratum to “What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability”	12
Design details for overdose education and take‐home naloxone kits: Codesign with family medicine, emergency department, addictions medicine and community	12
Tackling Inequalities in Access to Medicines for People Experiencing Homelessness: A Meta‐Ethnography and Qualitative Systematic Review	12
Patient preferences and choices as a reflection of trust—A cluster analysis comparing postsurgical perceptions in a private and a public hospital	12
Co‐Design of a Facilitated Self‐Management Toolkit for People With Parkinson's Disease	12
Ecologising Invited and Uninvited Patient Participation in Russia	12
A Patient and Public Engagement Project to Inform Dementia Care in a UK Hospital Trust	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
How to make mental health services more youth‐friendly? A Delphi study involving young adults, parents and professionals	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

Translation and Psychometric Evaluation in Cancer Care of the German Version of collaboRATETM—a 3‐item Patient‐reported Measure of Shared Decision‐Making	12
A rapid review of interventions to improve medicine self‐management for older people living at home	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
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Person‐centred sexual and reproductive health: A call for standardized measurement	12
Barriers and facilitators to engaging with a digital self‐management programme for painful distal upper limb musculoskeletal disorders: A qualitative exploratory 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	12
Co‐Authoring and Reporting on Lived Experience Engagement in Mental Health and/or Substance Research: A Qualitative Study and Guidance Document	12
Epistemic justice in public involvement and engagement: Creating conditions for impact	12
Evaluation of the Patient Innovation Partner Role: Perceived Benefits, Structures, Supports, and Recommendations for Lived Experience Engagement in Healthcare Innovation Teams	12
Stakeholder Perspectives on Built Environmental Factors to Support Stroke Rehabilitation and Return to Everyday Life	11
Talking the Walk (Along): Lessons Learned From Engaging With Children With Cerebral Palsy and Their Parents for Investigating Lived Experiences of Falls	11
Compound impact of cognitive and physical decline: A qualitative interview study of people with Parkinson's and cognitive impairment, caregivers and professionals	11
Involving Knowledge Users in Health Services Research: Collective Reflections and Learning From a National Evaluation of Recurrent Miscarriage Services	11
Empowerment, Participation, and Person‐Centeredness as Prerequisites for Health‐Promoting Settings in Everyday Practice: A Swedish Case Study	11
Implementing peer support work in mental health care in Germany: The methodological framework of the collaborative, participatory, mixed‐methods study (ImpPeer‐Psy5)	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
Increasing Youth Peer Workers' Impact Through Integration: Peer Worker Perspectives on Best Practice in Youth Mental Health	11
Structuring healthcare advance directives: Evidence from Chinese end‐of‐life cancer patients' treatment preferences	11
Coproducing an Ecological Momentary Assessment Measurement Burst Mental Health Study With Young People: The MHIM Coproduction Protocol	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
‘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	11
Exploring the Views of Children With Cerebral Palsy, Their Parents and Physiotherapists on Participating in a Feasibility Randomised Controlled Trial Testing an Exergaming Device: A Qualitative Study	11
More than a feeling? What does compassion in healthcare ‘look like’ to patients?	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
Co‐designing resources to support older people with intellectual disabilities and their families plan for parental death and transitions in care	11
Multimodal Analysis of Stories Told by Mental Health Influencers on TikTok	11
A Mixed Methods Evaluation of the Statutory Duty of Candour in Victorian Health Services: Study Protocol	11
Sleep hygiene behaviours mediate the association between health/e‐health literacy and mental wellbeing	11
An Interactive Vision‐Based 3D Augmented Reality System for In‐Home Physical Rehabilitation: A Qualitative Inquiry to Inform System Development	11
Involving Societal Stakeholders in Dementia Risk Reduction: An Explorative Study	11
A Longitudinal Qualitative Study of Resourcefulness Training Needs During the Hospital‐to‐Home Transition After Stroke in Young and Middle‐Aged Adults	11
Cognitive Communication, Voice and Swallowing Difficulties Experienced by Adults With Long‐COVID: A Scoping Review	11
Effects of a shared decision‐making implementation programme on patient‐centred communication in oncology—Secondary analysis of a randomised controlled trial	11
Challenges of Inclusion: A Population‐Based Interview Study of Long Covid	10
Adapting a codesign process with young people to prioritize outcomes for a systematic review of interventions to prevent self‐harm and suicide	10
Employing cofacilitation to balance power and priorities during health service codesign	10
The importance of personal documentation for patients living with long‐term illness symptoms after pituitary surgery: A Constructivist Grounded Theory study	10
Patient versus physician preferences for lipid‐lowering drug therapy: A discrete choice experiment	10
Behind the Screen: An Exploratory Study of Factors Influencing Breast Screening Uptake in Lancashire (UK)	10
Patient and Public Involvement (PPI) in Secondary Data Analysis: Protocol for a Targeted Review	10
Patients' and Therapists' Views of Integrated Online CBT for Depression	10
Issue Information	10
Co‐Creation Methodology for Developing a Racial Inclusivity Training Resource in Physiotherapy Education	10
Public Contribution in Qualitative Research With Parents of Children Treated for Cancer: Description of and Reflections on a Collaborative Data Analysis Approach	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	10
‘When a patient chooses to die at home, that's what they want… comfort, home’: Brilliance in community‐based palliative care nursing	10
Widening or narrowing inequalities? The equity implications of digital tools to support COVID‐19 contact tracing: A qualitative study	10
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User Input in the Development of Digital Sexual Health Tools: A Scoping Review and Guidance for Tool Developers	10
Frameworks Used to Engage Postsecondary Students in Campus Mental Health Research: A Scoping Review	10
The Acceptability, Safety and Impact of a Play Co‐Developed With Public Contributors as a Format for Disseminating Research on a Sensitive Subject	10
Factors Influencing Kidney Transplantation Experiences for Patients From Culturally and Linguistically Diverse Backgrounds: A Qualitative Study	10
Factors affecting patients' journey with primary healthcare services during mental health‐related sick leave	9
Overarching Priorities for Health and Care Research in the United Kingdom: A Coproduced Synthesis of James Lind Alliance ‘Top 10s’	9
Recommendations for community pharmacy to improve access to medication advice for people from ethnic minority communities: A qualitative person‐centred codesign study	9
Comparing an in‐person workshop and a postal Delphi survey for involving health service users in health care and health research prioritization	9
Ten Priorities for Research Addressing the Intersections of Brain Injury, Mental Health and Addictions: A Stakeholder‐Driven Priority‐Setting Study	9
Erratum	9
A co‐created multimethod evaluation of recovery education in Ireland	9
Engaging with Culturally and Linguistically Diverse Communities to Promote Palliative Care That Exceeds Expectation	9
(Re)constructing identity following acquired brain injury: The complex journey of recovery after stroke	9
Co‐Designing an Engagement Strategy to Include the Voices of a Minority Group in Assessing the Quality of Maternity and Neonatal Care	9
Family caregiver roles and challenges in assisting patients with cancer treatment decision‐making: Analysis of data from a national survey	9
Engagement With Professional Stakeholders in Healthcare Research—The Case of the Dementia PersonAlised Care Team (D‐PACT) Project in the United Kingdom	9
What Do We Know About Sharing Power in Co‐Production in Mental Health Research? A Systematic Review and Thematic Synthesis	9
‘A Forever Imprint on Me…I Couldn't Be There When He Needed Me the Most’: Care Partner Experiences of Patient Safety During Covid‐19 Restrictions	9
Recommendations for a Communication Strategy to Support Informed Decision‐Making About Self or Clinician Sampling for Cervical Screening in the UK: Qualitative Study	9
The Bidirectional Engagement and Equity (BEE) Research Framework to Guide Community–Academic Partnerships: Developed From a Narrative Review and Diverse Stakeholder Perspectives	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
Lived Experiences of Returning to Participation After Mild Stroke: A Phenomenological Study in Spain	9
Co‐building a training programme to facilitate patient, family and community partnership on research grants: A patient‐oriented research project	9
Living With the Fear of Recurrence in Benign Paroxysmal Positional Vertigo	9
Exploring the barriers and facilitators to volunteering as an intervention for those with long‐term neurological conditions: How make therapeutic volunteering possible?	9
Co‐ideation and co‐design in co‐creation research: Reflections from the ‘Co‐Creating Safe Spaces’ 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
The psychological consequences of living with coronary heart disease: Are patients' psychological needs served? A mixed‐method study in Germany	9
A Pre–Post Study of the Feasibility, Acceptability and Benefits of a Co‐Design Approach for the Development of a Digital Suicide Prevention App for International Students	9
Co‐Design of a Framework for Person‐Centred Care at Emergency Department Triage and Waiting Room	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
Defining Health Movements and Health Needs Across the Life Course: A Qualitative Study	9
Optimizing the design and implementation of question prompt lists to support person‐centred care: A scoping review	9
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	9
Correction to “Creating Safer Cancer Care With Ethnic Minority Patients: A Qualitative Analysis of the Experiences of Cancer Service Staff”	9
Adolescent Involvement in Co‐Authoring Peer Reviewed Publications: A Reflection of Challenges and Best Practice Recommendations	9
How Do Australians Manage Diagnostic Testing Risks? Focus Groups Linked to a Model of Behaviour Change	9
How Do We Get the Public Into Public Health Research? Learnings and Key Recommendations From Initiating a Community Involvement Project Scheme	9
Engagement of People With Lived Experience in Spinal Cord Injury to Address Innovation Priorities	9
Understanding the Role of Patients and Carers in a Virtual Hospital Through Journey Mapping: Multi‐Method Triangulation Analysis	9
Perceptions of the Impact of Comorbidity on the Bowel Cancer Screening Programme: Qualitative Study With Bowel Screening Participants and Staff	9
Women's experiences along the ovarian cancer diagnostic pathway in Catalonia: A qualitative study	9
Item development for a patient‐reported measure of compassionate healthcare in action	9