Health Expectations

Article	Citations
	156
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	135
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	133
Patient preferences for heart valve disease intervention	91
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	84
Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey	82
Look on the Bright Side: The Interactional Construction of a Survivor Identity in the Breast Cancer Clinic	71
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	55
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	51
What Supports and Constrains the Implementation of Robust and Rapid Evaluation Within Local Government Public Health Systems?	51
From Co‐Design to Quality Improvement: Using the Double Diamond Framework to Develop Primary Care Redesign Priorities for Hypertension Care	50
Co‐Design of a Community of Practice for People With Personal and Professional Expertise or Interest in Dementia in Australia	49
Co‐Developing User‐Centred Nutrition Educational Resources to Integrate Nutrition Into Multiple Sclerosis Care: A Collaborative Approach With Healthcare Professionals and Healthcare Consumers	46
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	45
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice	43
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	41
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	41
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	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
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	38
Ripple Effects Mapping: Evaluating Multilevel Perspectives and Impacts of a Statewide Community–Academic Partnership Network on Covid‐19 Health Disparities	36
Identification and Applications of Key Elements in the Development of Pictorial Support for People With Aphasia After Stroke: A Co‐Design Approach	34
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	34
Powerless or Powerful? Healthcare Professionals' Construction of Agency in Patient and Family Engagement Accounts	32
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	30

Continuity Is Essential: The Experiences of Co‐Design Participants During the Implementation of a New Health Service	30
Indicators for adequate diabetes care for the indigenous communities of Ecuador	29
Participatory research with carers: A systematic review and narrative synthesis	29
Psychosocial Impact of Breast Density Notification Through Breast Cancer Screening: A Qualitative Interview Study	29
Authors' Response to the Letter by Sun et al.	27
Children's Communication Choices About Musculoskeletal Pain and Injury: Insights From a Public Involvement Event	27
Youth engagement in mental health research: A systematic review	27
Exploring Medication Safety in Transitions From Prison to Community: A Qualitative Study	27
Identifying Common Patient‐Oriented Priorities for Child and Adolescent Health Research and Care: A Systematic Review of Priority Setting Partnerships	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	26
A Co‐Produced Health Literacy Programme for Pregnant Women Whose First Language Is Not English: A Qualitative Study of Women's Experiences	26
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	26
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	25
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	25
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	25
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	25
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs	24
Co‐Designing a Culturally Tailored Nutrition Resource With African Migrant Women and Healthcare Professionals in Australia	24
Just a story? Leadership, lived experience and integrated care	24
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	23
Mobilising Knowledge for General Practice Decarbonisation: Maximising Impact Through a Multi‐Stakeholder Workshop	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
HIV Care Seeking Pathways and Barriers to the Continuum of Care Faced by Persons Living With HIV in Rural Nepal: A Qualitative Study	22
A Qualitative Evaluation Exploring Co‐Production of Falls Management in Care Homes	22
Partnering With Patients to Conduct High‐Quality Research – Where Have We Been and Where Are We Going?	22
Agenda Setting in Outpatient Consultation of Older Adults With Long‐COVID	22
People With Non‐Communicable Diseases Using Ayurveda: A UK‐Based Qualitative Study	22
‘But … Would I Be Able to Toast With Friends?’ When Service Users Ask for New Care Pathways	22
Knowledge Families Hold: Co‐Production and Co‐Research With Mental Health Family Carers in Understanding Experiences During the COVID‐19 Pandemic	21
The interactive dimensions of encounters in HIV care: From trauma to relational traumatic growth	21
Patient and Staff Insights on Digital Care Pathways for Patients With Low Back Pain in the Emergency Department: A Qualitative Study	21
Reflections on the opportunities and challenges of applying experience‐based co‐design (EBCD) to phase 1 clinical trials in oncology	21
‘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	21
Perceptions and Significance of Long Covid Diagnoses From the Perspectives of Children and Young People With Long Covid, Their Parents and Professionals	20
Content validity testing of the INTERMED Self‐Assessment in a sample of adults with rheumatoid arthritis and rheumatology healthcare providers	20
Announcements of Death During the COVID‐19 Pandemic: A Qualitative Study of Family Experiences	20
How we define recurrent miscarriage matters: A qualitative exploration of the views of people with professional or lived experience	20
Uncovering the Dynamic System Driving Older Adults' Vitality: A Causal Loop Diagram Co‐Created With Dutch Older Adults	19
Assessing the environment for engagement in health services: The Audit for Consumer Engagement (ACE) tool	19
‘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	19
Illness Expectations and Asthma Symptoms: A 6‐Month Longitudinal Study	19
Community Health Workers' and Pharmacists' Perspectives of a CHW‐Pharmacist Collaboration Model to Support Medication Adherence	19
Developing an Inclusive Dance Guide for Children With Cerebral Palsy: A Co‐Design Process and Initial Feasibility Study	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
A Youth‐Led Evaluation of Adolescent Involvement in a Project on Development of Guidelines for Adolescent Involvement in Health Research	19
‘Lifts your spirits, lifts your mind’: A co‐produced mixed‐methods exploration of the benefits of green and blue spaces for mental wellbeing	19
Hospital Food Service Experiences Between Older Patients From English‐ and Non‐English Speaking Backgrounds in a Large Public Hospital in Australia: A Qualitative Analysis	18
‘Physical well‐being is our top priority’: Healthcare professionals' challenges in supporting psychosocial well‐being in stroke services	18
Experiences and expectations of receiving volunteer services among home‐based elderly in Chinese urban areas: 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
Contextualisation of the safeTALK™ Suicide Prevention Program: A Descriptive Qualitative Study	18
Behaviour, barriers and facilitators of shared decision making in breast cancer surgical treatment: A qualitative systematic review using a ‘Best Fit’ framework approach	18
Exploring the lived experience of receiving mental health crisis care at emergency departments, crisis phone lines and crisis care alternatives	17
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	17
‘I Would Feel Failed By the Medical Community Entirely’: Transgender Americans' Calls for Advocacy From Health Professionals in a Care‐Restricted World	17
How Lived Experience Advisory Groups Contribute to the Design and Conduct of Mental Health Research	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
The experiences of psychiatric patients, their caregivers and companions in upholding patient dignity during hospitalization: A qualitative study	17
‘I Battle With This Gambling Addiction Every Day’. Learning From Lived Experiences of Recovery to Guide Gambling Harm Prevention Strategies	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
Counting the Cost: The Hidden Financial Realities of Neuromuscular Disease Through Patient and Family Perspectives	17
The IMPROV Project: Protocol for Using a Modified Nominal Group Technique to Prioritise Oral Health Promotion Strategies With the Karen Refugee Community in Victoria	17
Provision of and trust in COVID‐19 vaccines information: Perspectives of people who have had COVID‐19	16
Patient perspectives on primary care for multimorbidity: An integrative review	16
Integrating Clinical Perspectives in the Prevention of Teenage Pregnancy	16
Consumer Experience of an Australian Multidisciplinary Long COVID Clinic That Incorporates Personalised Exercise Prescription: A Qualitative Analysis	16
Prevalence of Hearing, Vision and Cognitive Impairment and Impact in Older Adults in Home Care: A Study Protocol	16
Experiences and Perceptions of Self‐Harm in Rural‐Dwelling Adults: A Rapid Review of Qualitative Evidence	16
Involving People With Lived Experience in Electronic Health Record Database Studies Reflections and Learning From the CHOOSE Study	16
Women's experiences of care after stillbirth and obstetric fistula: A phenomenological study in Kenya	16
Perceptions of HIV‐Related Stigma Among Youth Exposed to the PPSAC Programme in Yaoundé, Cameroon	16
Reply to: Amplifying Women's Voices in Menopause Research: The Importance of Inclusive Perspectives [Letter]	16
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	16
Understanding the cultural environment of the outpatient care setting for patients with dementia receiving cancer treatment: A qualitative study	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
Development of person‐centred quality indicators for aged care assessment services in Australia: A mixed methods study	16
Gender bias in shared decision‐making among cancer care guidelines: A systematic review	16
Engaging Culturally and Linguistically Diverse Communities to Prepare for Lung Cancer Screening Implementation in Australia: A Qualitative Focus Group Study	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
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
Children's behavioural and emotional reactions towards living with congenital heart disease in Saudi Arabia: A grounded theory study	16
Investigating the Applicability of the SAFER‐YCL Care Bundle for Transitions From CAMHS Crisis and Liaison Services: The Barriers and Enablers	15
The HUSH Project: Using codesign to reduce sleep disruptions for patients in hospital	15
Problem‐based shared decision making: The role of canonical SDM steps	15
Public and Patient Involvement in Artificial Intelligence and Big Data Healthcare Research: An Exploration of Issues and Challenges Within the AI‐Multiply Project	15
Family Interviews Improve Health Service Recommendations in Mortality Review Process: A Mixed‐Methods Assessment	15
Participatory approaches for developing a practical handbook integrating health information for supporting individuals with mild cognitive impairment and their families	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
What Drives Public Preference for Rare Drugs Coverage in China? Insights From a Multi‐Center Discrete Choice Experiment	15
Cultural Adaptations of Healthcare Interventions: A Step‐by‐Step Guide	15
Co‐Creation in Research: Further Reflections From the ‘Co‐Creating Safe Spaces’ Project	15
Developing a Women's Thought Collective methodology for health research: The roles and responsibilities of researchers in the reflexive co‐production of knowledge	15
Telemedicine and Cultural Competency in Dementia Care: Mapping Stakeholder Roles in Digital Toolkit Development in SSA: A Systematic Review	14
Long COVID and Health Inequalities: What's Next for Research and Policy Advocacy?	14
Exiting Surveillance From Abdominal Aortic Aneurysm Screening: The Views of Clinicians, and Men in Surveillance and Their Family Members	14
Co‐Producing Personalised Discharge Planning: Developing a Toolkit to Improve Caregiver Involvement in Hospital Transitions	14
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	14
Co‐Design of an Ecosystem of Services to Support Veteran Well‐Being and Reduce Excessive Alcohol Consumption	14
Issue Information	14
Barriers and facilitators to engaging with a digital self‐management programme for painful distal upper limb musculoskeletal disorders: A qualitative exploratory study	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	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
Feasibility and Acceptability of an Incentive‐Based Intervention for Health Behaviour Change Among Rural Residents in China: A Mixed‐Methods Evaluation	14
The value of using patient‐reported outcomes for health screening during long‐term follow‐up after paediatric stem cell transplantation for nonmalignant diseases	14
Challenges and Facilitators to Patient and Public Involvement In Stroke Research: Protocol for 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”	14
Co‐Designing Lived Experience Guide Support for First Responder Mental Health: Defining the Role and Considerations for Implementation	14
Epidermolysis Bullosa in Spain: A Qualitative Analysis of Its Social Impact on Families With Diagnosed Minors	14
Living With Diabetes in Alberta: Patient and Caregiver Priorities for Diabetes Care, Management, and Treatment	14
Leveraging Community‐Based System Dynamics to Understand Long Covid Disparities in African American Communities: A Model for Health Equity Research	14
Participant and caregiver perspectives on health feedback from a healthy lifestyle check	14
A Proposal for Addressing Bioethical Concerns Along the 10‐Step Framework for Community Engagement	14
Implementing and Delivering Culturally Centred Pharmacy Services Tailored to Ethnically Minoritised Populations: A Qualitative Systematic Review and Meta‐Ethnography	13
Recognising Consumers' Contributions to Health Research: Co‐Designing a Remuneration Framework for the Australian Context	13
How Did Women From South Asian Backgrounds and People Seeking Asylum and Refugees Look After Their Health and the Health of Others During the COVID‐19 Pandemic? A Community Research Approach	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
Stakeholder Consultation to Establish Research Priorities for Specialist Dementia Nursing in the United Kingdom	13
Alignment of patient‐centredness definitions with real‐life patient and clinician experiences: A qualitative study	13
Progress Through Engagement: A Systematic Review and Thematic Synthesis of Qualitative Community‐Based Participatory Research in Vision Impairment	13
A systematic review of theories, models and frameworks used for youth engagement in health research	13
Stories From Black Women in Iowa About Reproductive Health Care Experiences, Self‐Advocacy, and Recommendations for Change	13
Building Trust in a Newly Established Physician–Patient Relationship: A Scoping Review	13
Person‐centred sexual and reproductive health: A call for standardized measurement	13
How Has ‘What Matters to You’ Been Used for Patient Care? A Scoping Review	13
Exploring Patient Understandings of Navigation Services Within Alberta's Healthcare System: A Qualitative Study	13
Family Carer Involvement in Dementia Care Research: A Scoping Review and Expert Consultation	13
How to make mental health services more youth‐friendly? A Delphi study involving young adults, parents and professionals	13
The ultimate question? Evaluating the use of Net Promoter Score in healthcare: A systematic review	13

Barriers to Care for Adults With Sickle Cell Disease: A Qualitative Descriptive Study	13
‘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	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
Community health worker outreach to farmworkers in rural North Carolina: Learning from adaptations to the SARS‐CoV‐2 pandemic	12
Erratum to “What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability”	12
Talking the Walk (Along): Lessons Learned From Engaging With Children With Cerebral Palsy and Their Parents for Investigating Lived Experiences of Falls	12
Ecologising Invited and Uninvited Patient Participation in Russia	12
A Longitudinal Qualitative Study of Resourcefulness Training Needs During the Hospital‐to‐Home Transition After Stroke in Young and Middle‐Aged Adults	12
Structuring healthcare advance directives: Evidence from Chinese end‐of‐life cancer patients' treatment preferences	12
Coproducing an Ecological Momentary Assessment Measurement Burst Mental Health Study With Young People: The MHIM Coproduction Protocol	12
Empowerment, Participation, and Person‐Centeredness as Prerequisites for Health‐Promoting Settings in Everyday Practice: A Swedish Case Study	12
An Interactive Vision‐Based 3D Augmented Reality System for In‐Home Physical Rehabilitation: A Qualitative Inquiry to Inform System Development	12
A Mixed Methods Evaluation of the Statutory Duty of Candour in Victorian Health Services: Study Protocol	12
Involving Knowledge Users in Health Services Research: Collective Reflections and Learning From a National Evaluation of Recurrent Miscarriage Services	12
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	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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Cognitive Communication, Voice and Swallowing Difficulties Experienced by Adults With Long‐COVID: A Scoping Review	12
The Safe Environment for Every Kid Model in the Swedish Child Health Services: Adoption and Introduction in a Healthcare Region	12
Increasing Youth Peer Workers' Impact Through Integration: Peer Worker Perspectives on Best Practice in Youth Mental Health	12
Tackling Inequalities in Access to Medicines for People Experiencing Homelessness: A Meta‐Ethnography and Qualitative Systematic Review	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
Compound impact of cognitive and physical decline: A qualitative interview study of people with Parkinson's and cognitive impairment, caregivers 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
A Patient and Public Engagement Project to Inform Dementia Care in a UK Hospital Trust	12
Translation and Validation of the Medication Understanding and Use Self‐Efficacy Scale Among Patients With Type 2 Diabetes in Taiwan	12
Effects of a shared decision‐making implementation programme on patient‐centred communication in oncology—Secondary analysis of a randomised controlled trial	12
Sleep hygiene behaviours mediate the association between health/e‐health literacy and mental wellbeing	12
Evaluation of the Patient Innovation Partner Role: Perceived Benefits, Structures, Supports, and Recommendations for Lived Experience Engagement in Healthcare Innovation Teams	12
User Input in the Development of Digital Sexual Health Tools: A Scoping Review and Guidance for Tool Developers	11
	11
What Matters Most: The Top 10 Child and Adolescent Cancer Research Priorities in Australia	11
Implementing peer support work in mental health care in Germany: The methodological framework of the collaborative, participatory, mixed‐methods study (ImpPeer‐Psy5)	11
Co‐Design of a Facilitated Self‐Management Toolkit for People With Parkinson's Disease	11
The healthcare needs and general practice utilization of people with acquired neurological disability and complex needs: A scoping review	11
Widening or narrowing inequalities? The equity implications of digital tools to support COVID‐19 contact tracing: A qualitative study	11
Assessing Unmet Social Needs in Multiple Sclerosis Care in Australia: A Qualitative Assessment of Feasibility, Barriers and Enablers	11
A rapid review of interventions to improve medicine self‐management for older people living at home	11
Co‐Authoring and Reporting on Lived Experience Engagement in Mental Health and/or Substance Research: A Qualitative Study and Guidance Document	11
Involving Societal Stakeholders in Dementia Risk Reduction: An Explorative Study	11
Patient and Public Involvement (PPI) in Secondary Data Analysis: Protocol for a Targeted Review	11
Stakeholder Perspectives on Built Environmental Factors to Support Stroke Rehabilitation and Return to Everyday Life	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
Co‐designing resources to support older people with intellectual disabilities and their families plan for parental death and transitions in care	11
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	10
Public Contribution in Qualitative Research With Parents of Children Treated for Cancer: Description of and Reflections on a Collaborative Data Analysis Approach	10
Behind the Screen: An Exploratory Study of Factors Influencing Breast Screening Uptake in Lancashire (UK)	10
The Bidirectional Engagement and Equity (BEE) Research Framework to Guide Community–Academic Partnerships: Developed From a Narrative Review and Diverse Stakeholder Perspectives	10
Patient versus physician preferences for lipid‐lowering drug therapy: A discrete choice experiment	10
Frameworks Used to Engage Postsecondary Students in Campus Mental Health Research: A Scoping Review	10
Overarching Priorities for Health and Care Research in the United Kingdom: A Coproduced Synthesis of James Lind Alliance ‘Top 10s’	10
Causes, Solutions and Health Inequalities: Comparing Perspectives of Professional Stakeholders and Community Participants Experiencing Low Income and Poor Health in London	10
Listening to Women's Voices: A Patient and Public Involvement Exercise Exploring Vulval Reconstructive Surgery for UK Women With Female Genital Mutilation (FGM)	10
Comparing an in‐person workshop and a postal Delphi survey for involving health service users in health care and health research prioritization	10
Factors Influencing Kidney Transplantation Experiences for Patients From Culturally and Linguistically Diverse Backgrounds: A Qualitative Study	10
(Re)constructing identity following acquired brain injury: The complex journey of recovery after stroke	10
How Do We Get the Public Into Public Health Research? Learnings and Key Recommendations From Initiating a Community Involvement Project Scheme	10
Managing Asthma Well and Sustainably – Patient Perspectives Explored	10
Defining Health Movements and Health Needs Across the Life Course: A Qualitative Study	10
The importance of personal documentation for patients living with long‐term illness symptoms after pituitary surgery: A Constructivist Grounded Theory study	10
‘When a patient chooses to die at home, that's what they want… comfort, home’: Brilliance in community‐based palliative care nursing	10
Adolescent Involvement in Co‐Authoring Peer Reviewed Publications: A Reflection of Challenges and Best Practice Recommendations	10
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	10
Factors affecting patients' journey with primary healthcare services during mental health‐related sick leave	10
Understanding the Role of Patients and Carers in a Virtual Hospital Through Journey Mapping: Multi‐Method Triangulation Analysis	10
Issue Information	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
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
Women's experiences along the ovarian cancer diagnostic pathway in Catalonia: A qualitative study	10
What Do We Know About Sharing Power in Co‐Production in Mental Health Research? A Systematic Review and Thematic Synthesis	10
Recommendations for community pharmacy to improve access to medication advice for people from ethnic minority communities: A qualitative person‐centred codesign study	10
Ten Priorities for Research Addressing the Intersections of Brain Injury, Mental Health and Addictions: A Stakeholder‐Driven Priority‐Setting Study	10
Lived Experiences of Returning to Participation After Mild Stroke: A Phenomenological Study in Spain	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
Co‐Creation Methodology for Developing a Racial Inclusivity Training Resource in Physiotherapy Education	10
Item development for a patient‐reported measure of compassionate healthcare in action	9
Engaging with Culturally and Linguistically Diverse Communities to Promote Palliative Care That Exceeds Expectation	9
Living With the Fear of Recurrence in Benign Paroxysmal Positional Vertigo	9
Issue Information	9
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	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
Towards understanding and improving medication safety for patients with mental illness in primary care: A multimethod study	9
‘Beyond the Prescription’: An Arts‐Based Study of Older Adults Living With HIV and Their Primary Care Experiences in Ontario	9
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	9
Co‐Designing an Engagement Strategy to Include the Voices of a Minority Group in Assessing the Quality of Maternity and Neonatal Care	9
The psychological consequences of living with coronary heart disease: Are patients' psychological needs served? A mixed‐method study in Germany	9
Development and validation of educational multimedia to promote public health literacy about healthy cognitive aging	9
Engagement of People With Lived Experience in Spinal Cord Injury to Address Innovation Priorities	9
A qualitative evaluation of a co‐design process involving young people at risk of suicide	9
Perceptions of the Impact of Comorbidity on the Bowel Cancer Screening Programme: Qualitative Study With Bowel Screening Participants and Staff	9
What really is nontokenistic fully inclusive patient and public involvement/engagement in research?	9
Co‐Design of a Framework for Person‐Centred Care at Emergency Department Triage and Waiting Room	9
Conceptual and practical challenges associated with understanding patient safety within community‐based mental health services	9