Health Expectations

Article	Citations
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	178
Feasibility of a best–worst scaling exercise to set priorities for autism research	138
	100
Just a story? Leadership, lived experience and integrated care	98
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	93
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	87
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	71
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	67
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	66
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	54
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	50
Identification and Applications of Key Elements in the Development of Pictorial Support for People With Aphasia After Stroke: A Co‐Design Approach	42
Continuity Is Essential: The Experiences of Co‐Design Participants During the Implementation of a New Health Service	40
Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey	39
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	38
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers	38
Children's Communication Choices About Musculoskeletal Pain and Injury: Insights From a Public Involvement Event	35
Youth engagement in mental health research: A systematic review	35
Participatory research with carers: A systematic review and narrative synthesis	34
Identifying Common Patient‐Oriented Priorities for Child and Adolescent Health Research and Care: A Systematic Review of Priority Setting Partnerships	34
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	34
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs	33
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice	32
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	32
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	31

Indicators for adequate diabetes care for the indigenous communities of Ecuador	30
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	29
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	29
Inside Front Cover: Volume 25 Issue 1	28
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	28
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	28
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
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	27
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	26
Patient preferences for heart valve disease intervention	26
Ripple Effects Mapping: Evaluating Multilevel Perspectives and Impacts of a Statewide Community–Academic Partnership Network on Covid‐19 Health Disparities	26
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	26
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	25
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	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
HIV Care Seeking Pathways and Barriers to the Continuum of Care Faced by Persons Living With HIV in Rural Nepal: A Qualitative Study	24
‘Lifts your spirits, lifts your mind’: A co‐produced mixed‐methods exploration of the benefits of green and blue spaces for mental wellbeing	23
The Challenging Process of Developing an Antenatal Social Intervention for Parents From Culturally Diverse Backgrounds to Reduce Postnatal Distress: A Participatory Action Research Study	23
Knowledge Families Hold: Co‐Production and Co‐Research With Mental Health Family Carers in Understanding Experiences During the COVID‐19 Pandemic	23
‘They need to ask me first’. Community engagement with low‐income citizens. A realist qualitative case‐study	22
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
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	19
The interactive dimensions of encounters in HIV care: From trauma to relational traumatic growth	19
Assessing the environment for engagement in health services: The Audit for Consumer Engagement (ACE) tool	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
Patient and Staff Insights on Digital Care Pathways for Patients With Low Back Pain in the Emergency Department: A Qualitative Study	19
‘But … Would I Be Able to Toast With Friends?’ When Service Users Ask for New Care Pathways	19
Content validity testing of the INTERMED Self‐Assessment in a sample of adults with rheumatoid arthritis and rheumatology healthcare providers	19
Partnering With Patients to Conduct High‐Quality Research – Where Have We Been and Where Are We Going?	18
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
The experiences of psychiatric patients, their caregivers and companions in upholding patient dignity during hospitalization: A qualitative study	18
Announcements of Death During the COVID‐19 Pandemic: A Qualitative Study of Family Experiences	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
Person‐centred caregiver singing for people living with dementia in South Africa: A mixed methods evaluation of acceptability, feasibility, and professional caregivers' experiences	18
Perceptions and Significance of Long Covid Diagnoses From the Perspectives of Children and Young People With Long Covid, Their Parents and Professionals	17
‘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	17
Evaluation of aspiration risk by relatives of inpatients in the neurology service: A metaphor analysis	17
Illness Expectations and Asthma Symptoms: A 6‐Month Longitudinal Study	17
Reflections on the opportunities and challenges of applying experience‐based co‐design (EBCD) to phase 1 clinical trials in oncology	17
How we define recurrent miscarriage matters: A qualitative exploration of the views of people with professional or lived experience	17
Developing an Inclusive Dance Guide for Children With Cerebral Palsy: A Co‐Design Process and Initial Feasibility Study	17
Uncovering the Dynamic System Driving Older Adults' Vitality: A Causal Loop Diagram Co‐Created With Dutch Older Adults	17
Exploring the lived experience of receiving mental health crisis care at emergency departments, crisis phone lines and crisis care alternatives	17
‘Physical well‐being is our top priority’: Healthcare professionals' challenges in supporting psychosocial well‐being in stroke services	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
Problem‐based shared decision making: The role of canonical SDM steps	16

Needs assessment for health service design for people with back pain in a hospital setting: A qualitative study	16
Provision of and trust in COVID‐19 vaccines information: Perspectives of people who have had COVID‐19	16
Experiences and expectations of receiving volunteer services among home‐based elderly in Chinese urban areas: A qualitative study	16
Family Interviews Improve Health Service Recommendations in Mortality Review Process: A Mixed‐Methods Assessment	16
Children's behavioural and emotional reactions towards living with congenital heart disease in Saudi Arabia: A grounded theory study	16
Co‐Creation in Research: Further Reflections From the ‘Co‐Creating Safe Spaces’ Project	16
Gender bias in shared decision‐making among cancer care guidelines: A systematic review	15
The influence of social relationships and activities on the health of adults with obesity: A qualitative study	15
Women's experiences of care after stillbirth and obstetric fistula: A phenomenological study in Kenya	15
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	15
Understanding the cultural environment of the outpatient care setting for patients with dementia receiving cancer treatment: A qualitative study	15
Reply to: Amplifying Women's Voices in Menopause Research: The Importance of Inclusive Perspectives [Letter]	15
Developing a Women's Thought Collective methodology for health research: The roles and responsibilities of researchers in the reflexive co‐production of knowledge	14
Issue Information	14
Development of person‐centred quality indicators for aged care assessment services in Australia: A mixed methods study	14
Involving People With Lived Experience in Electronic Health Record Database Studies Reflections and Learning From the CHOOSE Study	14
Participatory approaches for developing a practical handbook integrating health information for supporting individuals with mild cognitive impairment and their families	14
Patient perspectives on primary care for multimorbidity: An integrative review	14
Codesigning a patient support portal with health professionals and men with prostate cancer: An action research study	14
The HUSH Project: Using codesign to reduce sleep disruptions for patients in hospital	14
Consumer Experience of an Australian Multidisciplinary Long COVID Clinic That Incorporates Personalised Exercise Prescription: A Qualitative Analysis	14
Experiences and Perceptions of Self‐Harm in Rural‐Dwelling Adults: A Rapid Review of Qualitative Evidence	14
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	14
How to make mental health services more youth‐friendly? A Delphi study involving young adults, parents and professionals	13
Implementing and Delivering Culturally Centred Pharmacy Services Tailored to Ethnically Minoritised Populations: A Qualitative Systematic Review and Meta‐Ethnography	13
Challenges and Facilitators to Patient and Public Involvement In Stroke Research: Protocol for a Qualitative Study	13
Long COVID and Health Inequalities: What's Next for Research and Policy Advocacy?	13
Comparative analysis of centrally mediated and inflammatory pain experiences amongst patients diagnosed with rheumatoid arthritis: A multimethods study	13
The ultimate question? Evaluating the use of Net Promoter Score in healthcare: A systematic review	13
Erratum to “Recruitment and Retention of Adolescents for an Ecological Momentary Assessment Measurement Burst Mental Health Study: The MHIM Engagement Strategy”	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
How Has ‘What Matters to You’ Been Used for Patient Care? A Scoping Review	13
Co‐Design of an Ecosystem of Services to Support Veteran Well‐Being and Reduce Excessive Alcohol Consumption	13
A systematic review of theories, models and frameworks used for youth engagement in health research	13
Centredness in health care: A systematic overview of reviews	13
Alignment of patient‐centredness definitions with real‐life patient and clinician experiences: A qualitative study	13
Participant and caregiver perspectives on health feedback from a healthy lifestyle check	13
Epidermolysis Bullosa in Spain: A Qualitative Analysis of Its Social Impact on Families With Diagnosed Minors	13
Barriers and facilitators to engaging with a digital self‐management programme for painful distal upper limb musculoskeletal disorders: A qualitative exploratory study	13
Exiting Surveillance From Abdominal Aortic Aneurysm Screening: The Views of Clinicians, and Men in Surveillance and Their Family Members	13
Stakeholder Consultation to Establish Research Priorities for Specialist Dementia Nursing in the United Kingdom	13
Codesigning person‐centred quality indicators with diverse communities: A qualitative patient engagement study	12
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	12
Sleep hygiene behaviours mediate the association between health/e‐health literacy and mental wellbeing	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
Recognising Consumers' Contributions to Health Research: Co‐Designing a Remuneration Framework for the Australian Context	12
Co‐Designing Lived Experience Guide Support for First Responder Mental Health: Defining the Role and Considerations for Implementation	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
Trends in the psychosocial and mental health of HIV‐positive women in China from 2015 to 2020: Results from two cross‐sectional surveys	12
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Exploring Patient Understandings of Navigation Services Within Alberta's Healthcare System: A Qualitative Study	12
Involvement of adolescent representatives and coresearchers in mental health research: Experiences from a research project	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
Issue Information	12
Structuring healthcare advance directives: Evidence from Chinese end‐of‐life cancer patients' treatment preferences	12
Person‐centred sexual and reproductive health: A call for standardized measurement	12
A Proposal for Addressing Bioethical Concerns Along the 10‐Step Framework for Community Engagement	12
Barriers to Care for Adults With Sickle Cell Disease: A Qualitative Descriptive Study	12
Ecologising Invited and Uninvited Patient Participation in Russia	11
Tackling Inequalities in Access to Medicines for People Experiencing Homelessness: A Meta‐Ethnography and Qualitative Systematic Review	11
Using focus groups to inform a peer health navigator service for people who are transgender and gender diverse in Saskatchewan, Canada	11
Coproducing an Ecological Momentary Assessment Measurement Burst Mental Health Study With Young People: The MHIM Coproduction Protocol	11
A Patient and Public Engagement Project to Inform Dementia Care in a UK Hospital Trust	11
Ethical issues experienced by persons with rheumatoid arthritis in a wearable‐enabled physical activity intervention study	11
Erratum to “What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability”	11
Evaluation of the Patient Innovation Partner Role: Perceived Benefits, Structures, Supports, and Recommendations for Lived Experience Engagement in Healthcare Innovation Teams	11
Translation and Validation of the Medication Understanding and Use Self‐Efficacy Scale Among Patients With Type 2 Diabetes in Taiwan	11
Epistemic justice in public involvement and engagement: Creating conditions for impact	11
How do consumers respond when presented with novel doctor performance information? A multivariate regression analysis	11
Patient preferences and choices as a reflection of trust—A cluster analysis comparing postsurgical perceptions in a private and a public hospital	11
Community health worker outreach to farmworkers in rural North Carolina: Learning from adaptations to the SARS‐CoV‐2 pandemic	11
The Safe Environment for Every Kid Model in the Swedish Child Health Services: Adoption and Introduction in a Healthcare Region	11
Involving Knowledge Users in Health Services Research: Collective Reflections and Learning From a National Evaluation of Recurrent Miscarriage Services	11
Design details for overdose education and take‐home naloxone kits: Codesign with family medicine, emergency department, addictions medicine and community	11
Effects of a shared decision‐making implementation programme on patient‐centred communication in oncology—Secondary analysis of a randomised controlled trial	11
An Interactive Vision‐Based 3D Augmented Reality System for In‐Home Physical Rehabilitation: A Qualitative Inquiry to Inform System Development	11
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	11
Corrigendum	10
Increasing Youth Peer Workers' Impact Through Integration: Peer Worker Perspectives on Best Practice in Youth Mental Health	10
Co‐Authoring and Reporting on Lived Experience Engagement in Mental Health and/or Substance Research: A Qualitative Study and Guidance Document	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
Co‐designing resources to support older people with intellectual disabilities and their families plan for parental death and transitions in care	10
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
Family caregiver roles and challenges in assisting patients with cancer treatment decision‐making: Analysis of data from a national survey	10
Multimodal Analysis of Stories Told by Mental Health Influencers on TikTok	10
Patient versus physician preferences for lipid‐lowering drug therapy: A discrete choice experiment	10
A Longitudinal Qualitative Study of Resourcefulness Training Needs During the Hospital‐to‐Home Transition After Stroke in Young and Middle‐Aged Adults	10
Co‐Creation Methodology for Developing a Racial Inclusivity Training Resource in Physiotherapy Education	10
The healthcare needs and general practice utilization of people with acquired neurological disability and complex needs: A scoping review	10
‘When a patient chooses to die at home, that's what they want… comfort, home’: Brilliance in community‐based palliative care nursing	10
Employing cofacilitation to balance power and priorities during health service codesign	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
More than a feeling? What does compassion in healthcare ‘look like’ to patients?	10
Implementing peer support work in mental health care in Germany: The methodological framework of the collaborative, participatory, mixed‐methods study (ImpPeer‐Psy5)	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
(Re)constructing identity following acquired brain injury: The complex journey of recovery after stroke	10
Adapting a codesign process with young people to prioritize outcomes for a systematic review of interventions to prevent self‐harm and suicide	10
Eliciting preferences for continuing medication among adult patients and parents of children with attention‐deficit hyperactivity disorder	10
Issue Information	10
A rapid review of interventions to improve medicine self‐management for older people living at home	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
Compound impact of cognitive and physical decline: A qualitative interview study of people with Parkinson's and cognitive impairment, caregivers and professionals	10
Adapting a conceptual framework to engage diverse stakeholders in genomic/precision medicine research	10
A Mixed Methods Evaluation of the Statutory Duty of Candour in Victorian Health Services: Study Protocol	10
Co‐Design of a Facilitated Self‐Management Toolkit for People With Parkinson's Disease	10
Issue Information	10
Stakeholder Perspectives on Built Environmental Factors to Support Stroke Rehabilitation and Return to Everyday Life	10
Patients' and Therapists' Views of Integrated Online CBT for Depression	10
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 Acceptability, Safety and Impact of a Play Co‐Developed With Public Contributors as a Format for Disseminating Research on a Sensitive Subject	9
Defining Health Movements and Health Needs Across the Life Course: A Qualitative Study	9
Causes, Solutions and Health Inequalities: Comparing Perspectives of Professional Stakeholders and Community Participants Experiencing Low Income and Poor Health in London	9
Recommendations for community pharmacy to improve access to medication advice for people from ethnic minority communities: A qualitative person‐centred codesign study	9
What Do We Know About Sharing Power in Co‐Production in Mental Health Research? A Systematic Review and Thematic Synthesis	9
Creating opportunities for patient participation in managing medications across transitions of care through formal and informal modes of communication	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
The importance of personal documentation for patients living with long‐term illness symptoms after pituitary surgery: A Constructivist Grounded Theory study	9
Ten Priorities for Research Addressing the Intersections of Brain Injury, Mental Health and Addictions: A Stakeholder‐Driven Priority‐Setting Study	9
Behind the Screen: An Exploratory Study of Factors Influencing Breast Screening Uptake in Lancashire (UK)	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
Recommendations for a Communication Strategy to Support Informed Decision‐Making About Self or Clinician Sampling for Cervical Screening in the UK: Qualitative Study	9
Optimizing the design and implementation of question prompt lists to support person‐centred care: A scoping review	9
Women's experiences along the ovarian cancer diagnostic pathway in Catalonia: A qualitative study	9
User Input in the Development of Digital Sexual Health Tools: A Scoping Review and Guidance for Tool Developers	9
Comparing an in‐person workshop and a postal Delphi survey for involving health service users in health care and health research prioritization	9
Pragmatism as a paradigm for patient‐oriented research	9
How Do We Get the Public Into Public Health Research? Learnings and Key Recommendations From Initiating a Community Involvement Project Scheme	9
Frameworks Used to Engage Postsecondary Students in Campus Mental Health Research: A Scoping Review	9
Factors affecting patients' journey with primary healthcare services during mental health‐related sick leave	9
Widening or narrowing inequalities? The equity implications of digital tools to support COVID‐19 contact tracing: A qualitative study	9
Overarching Priorities for Health and Care Research in the United Kingdom: A Coproduced Synthesis of James Lind Alliance ‘Top 10s’	9
Factors Influencing Kidney Transplantation Experiences for Patients From Culturally and Linguistically Diverse Backgrounds: A Qualitative Study	9
Challenges of Inclusion: A Population‐Based Interview Study of Long Covid	9
The Bidirectional Engagement and Equity (BEE) Research Framework to Guide Community–Academic Partnerships: Developed From a Narrative Review and Diverse Stakeholder Perspectives	9
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
Item development for a patient‐reported measure of compassionate healthcare in action	8
Using financial incentives to support service engagement of adults experiencing homelessness and mental illness: A qualitative analysis of key stakeholder perspectives	8
The psychological consequences of living with coronary heart disease: Are patients' psychological needs served? A mixed‐method study in Germany	8
Correction to “Creating Safer Cancer Care With Ethnic Minority Patients: A Qualitative Analysis of the Experiences of Cancer Service Staff”	8
A qualitative exploration of the barriers and facilitators affecting ethnic minority patient groups when accessing medicine review services: Perspectives of healthcare professionals	8
Engaging with Culturally and Linguistically Diverse Communities to Promote Palliative Care That Exceeds Expectation	8
Co‐Design of a Framework for Person‐Centred Care at Emergency Department Triage and Waiting Room	8
Co‐Designing an Engagement Strategy to Include the Voices of a Minority Group in Assessing the Quality of Maternity and Neonatal Care	8
Nothing about us without us: A co‐production strategy for communities, researchers and stakeholders to identify ways of improving health and reducing inequalities	8
Older Adults' Experiences and Expectations of Doctor–Patient Interactions During Early Hospital Care	8
Exploring the barriers and facilitators to volunteering as an intervention for those with long‐term neurological conditions: How make therapeutic volunteering possible?	8
Developing the Resident Measure of Safety in Care Homes (RMOS): A Delphi and Think Aloud Study	8
A qualitative evaluation of a co‐design process involving young people at risk of suicide	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
Reimagining consumer involvement: Resilient system indicators in the COVID‐19 pandemic response in New South Wales, Australia	8
Conceptual and practical challenges associated with understanding patient safety within community‐based mental health services	8
‘I just thought that it was such an impossible thing’: A qualitative study of barriers and facilitators to discontinuing long‐term use of benzodiazepine receptor agonists using the Theoretical Domains	8
Engagement of People With Lived Experience in Spinal Cord Injury to Address Innovation Priorities	8
What really is nontokenistic fully inclusive patient and public involvement/engagement in research?	8
Engagement With Professional Stakeholders in Healthcare Research—The Case of the Dementia PersonAlised Care Team (D‐PACT) Project in the United Kingdom	8
Perceptions of the Impact of Comorbidity on the Bowel Cancer Screening Programme: Qualitative Study With Bowel Screening Participants and Staff	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
Experiences, perceptions and expectations of health services amongst marginalized populations in urban Australia: A meta‐ethnographic review of the literature	8
Erratum	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
Towards understanding and improving medication safety for patients with mental illness in primary care: A multimethod study	8
Exploring the experiences and preferences of South Asian patients' of primary care in England since COVID‐19	8
Development and validation of educational multimedia to promote public health literacy about healthy cognitive aging	8
Co‐building a training programme to facilitate patient, family and community partnership on research grants: A patient‐oriented research project	8
A qualitative study assessing allied health provider perceptions of telepractice functionality in therapy delivery for people with disability	7
Developing a Set of Key Principles for Care Planning Within Older Adult Care Homes: A Modified Delphi Survey	7
Assessment of medication adherence, medication safety awareness and medication practice among patients with lung cancer: A multicentre cross‐sectional study	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
From polarity to plurality: Perceptions of COVID‐19 and policy measures in England and Scotland	7
Representation in participatory healthcare decision‐making	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
Transitional care decision‐making through the eyes of older people and informal caregivers: An in‐depth interview‐based study	7
Using World Cafés to engage an Australian culturally and linguistically diverse community around human papillomavirus vaccination	7