Health Expectations

Article	Citations
Developing a Quality Improvement Framework to Enhance the Health System User Experience for Individuals Living With Type 1 Diabetes: The Reshape T1D Study	361
A Socioecological Approach to Support the Transition to Adult Care for Youth With Medical Complexity: Family Perspectives and Recommendations	176
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	126
Community‐Driven Health Promotion: Evaluation of a Rural Microgrant Program	92
Healthcare Professionals' Responses to Complaints: A Qualitative Interview Study With Patients, Carers and Healthcare Professionals Using the Theoretical Domains Framework and COM‐B Model	83
Lived Experience and Family Engagement in Mental Health and Substance use Health Research: Case Profiles of Five Studies	72
Engaging with Culturally and Linguistically Diverse Communities to Promote Palliative Care That Exceeds Expectation	70
Delivery of Supported Self‐Management in Primary Care Asthma Reviews: Insights From the IMP2ART Programme	65
Engagement With Professional Stakeholders in Healthcare Research—The Case of the Dementia PersonAlised Care Team (D‐PACT) Project in the United Kingdom	54
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	53
Item development for a patient‐reported measure of compassionate healthcare in action	51
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	51
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	48
Perspectives of women living with type 1 diabetes regarding preconception and antenatal care: A qualitative evidence synthesis	47
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Barriers to preventive care utilization among Hong Kong community‐dwelling older people and their views on using financial incentives to improve preventive care utilization	42
The Time Moving exhibit: Exploring perceptions of time in end‐of‐life experiences	41
Public values to guide childhood vaccination mandates: A report on four Australian community juries	37
Development and validation of educational multimedia to promote public health literacy about healthy cognitive aging	37
Coproduction of a resource sharing public views of health inequalities: An example of inclusive public and patient involvement and engagement	36
A public and patient consultation process as an aid to design a person‐centred randomized clinical trial	35
Issue Information	31
Issue Information	31
Pathways to recovery model of youth substance misuse in Assam, India	30
Patient research priority setting partnership in human T‐cell lymphotropic virus type I	29

Awareness of diagnosis, treatment and risk of late effects in Chinese survivors of childhood cancer in Hong Kong	29
A qualitative exploration of the barriers and facilitators affecting ethnic minority patient groups when accessing medicine review services: Perspectives of healthcare professionals	28
The impact of expert by experience involvement in teaching in a DClinPsych programme; for trainees and experts by experience	26
Barriers and facilitators to mobile health and active surveillance use among older adults with skin disease	26
Exploring the barriers and facilitators to volunteering as an intervention for those with long‐term neurological conditions: How make therapeutic volunteering possible?	24
Issue Information	24
Experiences and perceptions of continuous deep sedation: An interview study among Dutch patients and relatives	24
Patient preferences for heart valve disease intervention	23
‘I am proud of how I handled it’. Exploring the impact of the COVID‐19 pandemic and related restrictions on well‐being of adults with severe mental illness using qualitative methods	23
Public and patient involvement in the development of an internet‐based guide for persistent somatic symptoms (GUIDE.PSS): A qualitative study on the needs of those affected	23
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Perceptions of recovery and rehabilitation in people with brain injury in Spain. A qualitative study	22
Issue Information	22
The Dilemmas and Opportunities of Co‐Creating Health Interventions to Fit Local Contexts: An Ethnographic Study on the Adaptation of Clinical Guidelines in Tanzania	22
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‘So Let's Go On Like This?’—Shared Decision‐Making and the Use of Outcome Information in Routine Care Management for People With Multiple Sclerosis	22
Operationalizing a patient engagement plan for health research: Sharing a codesigned planning template from a national clinical trial	21
Sociocultural influences on asthma self‐management in a multicultural society: A qualitative study amongst Malaysian adults	21
The psychological consequences of living with coronary heart disease: Are patients' psychological needs served? A mixed‐method study in Germany	21
Sexual Interventions in the Metaverse: Attitudes Towards Novel Therapeutic Approaches, a Qualitative Study	21
Reflections from the COVID‐19 pandemic on inequalities and patient and public involvement and engagement (PPIE) in social care, health and public health research	20
Recovery in Mind: A Recovery College's journey through the Covid‐19 pandemic	20
A challenge in qualitative research: Family members sitting in on interviews about sensitive subjects	20
Osteoarthritis management: Does the pharmacist play a role in bridging the gap between what patients actually know and what they ought to know? Insights from a national online survey	20
‘None of Them Know Me’: A Qualitative Study of the Implications of Locum Doctor Working for Patient Experience	20
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Barriers and facilitators of shared decision making in acutely ill inpatients with schizophrenia—Qualitative findings from the intervention group of a randomised‐controlled trial	19
Children's perspectives and experiences of the COVID‐19 pandemic and UK public health measures	19
Information, deliberation, and decisional control preferences for participation in medical decision‐making and its influencing factors among Chinese cancer patients	19
Preference‐based patient participation for most, if not all: A cross‐sectional study of patient participation amongst persons with end‐stage kidney disease	19
Adapting patient and public involvement in patient‐oriented methods research: Reflections in a Canadian setting during COVID‐19	19
Swallowing the pill of adverse effects: A qualitative study of patients' and pharmacists' experiences and decision‐making regarding the adverse effects of chronic pain medications	18
Engaging veteran stakeholders to identify patient‐centred research priorities for optimizing implementation of lung cancer screening	18
Perceptions of the Impact of Comorbidity on the Bowel Cancer Screening Programme: Qualitative Study With Bowel Screening Participants and Staff	18
‘You have to do what is best’: The lived reality of having a child who is repeatedly hospitalized because of acute lower respiratory infection	18
Inside Front Cover: Volume 25 Issue 1	18
‘It's Just Not Working’, a Qualitative Exploration of the Weight‐Related Healthcare Experiences of Individuals of Arab Heritage With Higher Weight in Australia	18
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	18
‘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	18
Building Relationships, Forming Collaborations: Lessons Learned From an Unconference Seeking to Cultivate Solutions in Healthcare	17
‘The Norm Is to Not Openly Collaborate’: Using the Lens of Co‐Production to Evaluate the Development of a COVID‐19 ICU Triage Policy	17
The Mediating Role of Students' Health Information Literacy Skills: Exploring the Relationship Between Web Resource Utilization and Health Information Evaluation Proficiency	17
Transitions: Living With Young‐Onset Alzheimer's Disease: A Qualitative Interview Study	17
A Qualitative Exploration of Stroke Survivors' Experiences of Using a Stroke Helpline	17
Participatory Design in Suicide Prevention: A Qualitative Study of International Students' Experiences of Adapting the LivingWorks safeTALK Programme	16
Public Perceptions of the Australian Health System During COVID‐19: Findings From a 2021 Survey Compared to Four Previous Surveys	16
Using financial incentives to support service engagement of adults experiencing homelessness and mental illness: A qualitative analysis of key stakeholder perspectives	16
Impact of Interventions on Medication Adherence in Patients With Coexisting Diabetes and Hypertension	15
Evaluating Experiences in a Digital Nutrition Education Program for People With Multiple Sclerosis: A Qualitative Study	15
How Do Australians Manage Diagnostic Testing Risks? Focus Groups Linked to a Model of Behaviour Change	15

Letter to the Editor: Best Practices on Public and Patient Involvement in Interprofessional Healthcare Education	15
Exploring Healthcare Paradoxes in Hospital Haemodialysis—A Qualitative Study	15
Exploring General Practitioners' Management of Self‐Harm in Young People: A Qualitative Study	15
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	15
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	15
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	15
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	15
Management of COVID‐19 and vaccination in Nepal: A qualitative study	14
Evaluating the benefit of early patient and public involvement for product development and testing with small companies	14
Experiences of human papillomavirus self‐sampling by women >60 years old: A qualitative study	14
Exploring COVID‐19 experiences for persons with multiple sclerosis and carers: An Australian qualitative study	14
Cancer survival stories: Perception, creation, and potential use case	14
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	14
Indicators for adequate diabetes care for the indigenous communities of Ecuador	14
Applying self‐determination theory towards motivational factors of physical activity in people undergoing haemodialyses: A qualitative interview study	14
Developing the Resident Measure of Safety in Care Homes (RMOS): A Delphi and Think Aloud Study	14
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	13
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	13
Conceptualization of patient‐centered care in Latin America: A scoping review	13
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	13
Identifying locally actionable strategies to increase participant acceptability and feasibility to participate in Phase I cancer clinical trials	13
Meaningful engagement through critical reflexivity: Engaging people with lived experience in continuing mental health professional development	13
The impact of adding cost information to a conversation aid to support shared decision making about low‐risk prostate cancer treatment: Results of a stepped‐wedge cluster randomised trial	13
‘A good decision is the one that feels right for me’: Codesign with patients to inform theoretical underpinning of a decision aid website	13
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	13
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	13
Trust and distrust in low‐income Michigan residents during the early COVID‐19 pandemic: A qualitative study	13
‘I wasn't made to feel like a nut case after all’: A qualitative story completion study exploring healthcare recipient and carer perceptions of good professional caregiving relationships	13
Exploring the sources of cervical cancer screening self‐efficacy among rural females: A qualitative study	13
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	12
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	12
Shaping research for people living with co‐existing mental and physical health conditions: A research priority setting initiative from the United Kingdom	12
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	12
Exploring the experiences and preferences of South Asian patients' of primary care in England since COVID‐19	12
Experiences of people with Long Covid with a digital physiotherapy intervention: A qualitative study	12
From Polarity to Plurality: Perceptions of COVID‐19 and Policy Measures in England and Scotland	12
‘We have no services for you… so you have to make the best out of it’: A qualitative study of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients’ dissatisfaction with healthcare services	12
Participatory research with carers: A systematic review and narrative synthesis	12
The acceptability of, and informational needs related to, self‐collection cervical screening among women of Indian descent living in Victoria, Australia: A qualitative study	12
Value in care: The contribution of supportive care to value‐based lung cancer services—A qualitative semistructured interview study	12
How and why do doctors communicate diagnostic uncertainty: An experimental vignette study	12
Creating safer cancer care with ethnic minority patients: A qualitative analysis of the experiences of cancer service staff	12
A co‐created multimethod evaluation of recovery education in Ireland	11
Partnered Recruitment: Engaging Individuals With Lived Experience in the Recruitment of Co‐Design Participants	11
Just a story? Leadership, lived experience and integrated care	11
What really is nontokenistic fully inclusive patient and public involvement/engagement in research?	11
Different views on collaboration between older persons, informal caregivers and care professionals	11
Rationalizing the Influence of Co‐Design on Distress, Clinical Decision‐Making and Disease Self‐Management of Cancer Patients‐as‐Partners: A Quasi‐Experimental Study	11
Embedding Public Involvement in a PhD Research Project With People Affected by Advanced Liver Disease	11
What aspects of health and wellbeing are most important to parent carers of children with disabilities?	11
Towards understanding and improving medication safety for patients with mental illness in primary care: A multimethod study	11
The psychosocial impact of a chronic disease in Ireland: Burdens and helpful practices for a life with epidermolysis bullosa	11
Validating care and treatment scenarios for measuring decisional conflict regarding future care preferences among older adults	11
Feasibility of a best–worst scaling exercise to set priorities for autism research	11
(Dis)trust in doctors and public and private healthcare institutions in the Western Balkans	10
A codevelopment process to advance methods for the use of patient‐reported outcome measures and patient‐reported experience measures with people who are homeless and experience chronic illness	10
Mixed methods evaluation to explore participant experiences of a pilot randomized trial to facilitate self‐management of people living with stroke: Inspiring virtual enabled resources following vascul	10
Development and psychometric testing of the patient participation in bedside handover survey	10
Conceptual and practical challenges associated with understanding patient safety within community‐based mental health services	10
A patient‐led, peer‐to‐peer qualitative study on the psychosocial relationship between young adults with inflammatory bowel disease and food	10
Rapid development of a COVID‐19 care planning decision‐aid for family carers of people living with dementia	10
Pilot trial of iBDecide: Evaluating an online tool to facilitate shared decision making for adolescents and young adults with ulcerative colitis	10
Reimagining consumer involvement: Resilient system indicators in the COVID‐19 pandemic response in New South Wales, Australia	10
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	10
Supporting the involvement of older adults with complex needs in evaluation of outcomes in long‐term care at home programmes	10
‘it was that … specialist … that finally listened to us … that's probably a weird answer to what you were expecting’: Clinician and carer perspectives on brilliant feeding care	10
What are the views of three key stakeholder groups on extending the breast screening interval for low‐risk women? A secondary qualitative analysis	10
Optimizing the implementation of lung cancer screening in Scotland: Focus group participant perspectives in the LUNGSCOT study	9
Correction to ‘Optimizing the design and implementation of question prompt lists to support person‐centred care: A scoping review’	9
Medicinal Cannabis and Consumer Vulnerability in Australia: A Nexus of Policy and Market Factors	9
Corrigendum	9
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	9
Understanding and Defining Young People's Involvement and Under‐Representation in Mental Health Research: A Delphi Study	9
What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability	9
My Wellbeing Journal: Development of a communication and goal‐setting tool to improve care for older adults with chronic conditions and multimorbidity	9
The CORE study—An adapted mental health experience codesign intervention to improve psychosocial recovery for people with severe mental illness: A stepped wedge cluster randomized‐controlled trial	9
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs	9
Exploring Stakeholder Roles and Strategies for Preventing Teenage Pregnancy: A Comprehensive Analysis in Lepelle‐Nkumpi District: South Africa	9
Patients', carers' and healthcare providers' views of patient‐held health records in Kerala, India: A qualitative exploratory study	9
Best Practices Guidelines for the Engagement of People With Lived Experience and Family Members in Mental Health and Substance Use Health Research: A Modified Delphi Consensus Study	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
Exploring first‐time mothers' experiences and knowledge about behavioural risk factors for stillbirth	9
Sharing administrative health data with private industry: A report on two citizens' juries	9
Amplifying Women's Voices in Menopause Research: The Importance of Inclusive Perspectives	9
The elephant in the room: Exploring the influence and participation of patients in infection‐related care across surgical pathways in South Africa and India	9
Taking a Pause: Co‐Designing a Reflection Tool for Meaning Creation in Patients With Type 2 Diabetes	9
Qualitative Exploration of Speech Pathologists' Experiences and Priorities for Aphasia Service Design: Initial Stage of an Experience‐Based Co‐Design Project to Improve Aphasia Services	9
Co‐ideation and co‐design in co‐creation research: Reflections from the ‘Co‐Creating Safe Spaces’ project	9
Community Preferences for Allied Health Services in Residential Aged Care	9
How is patient‐centred care conceptualized in obstetrical health? comparison of themes from concept analyses in obstetrical health‐ and patient‐centred care	9
“After Cutting It, Things Have Never Remained the Same”: A Qualitative Study of the Perspectives of Amputees and Their Caregivers	9
Erratum to: “The Bidirectional Engagement and Equity (BEE) Research Framework to Guide Community‐Academic Partnerships: Developed From a Narrative Review and Diverse Stakeholder Perspectives”	9
Prioritizing Chinese medicine clinical research questions in cancer palliative care from patient and caregiver perspectives	9
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Erratum	9
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	9
A Decision Aid for Patients Considering Surgery for Sciatica: Codesign and User‐Testing With Patients and Clinicians	9
The lived experience of weight loss maintenance in young people	9
Self‐management interventions for children and young people with sickle cell disease: A systematic review	9
My child is growing and now? Exploring the environmental needs of children with congenital Zika syndrome according to their caregivers' perceptions	8
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‘It Makes You Sit Back and Think Where You Wanna Go’: Veteran experiences in virtual whole health peer‐led groups	8
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	8
Lived experience engagement in mental health research: Recommendations for a terminology shift	8
Family carers' experiences and perceived roles in interprofessional collaborative practice in primary care: A constructivist grounded theory study	8
‘Advocacy groups are the connectors’: Experiences and contributions of rare disease patient organization leaders in advanced neurotherapeutics	8
Co‐building a training programme to facilitate patient, family and community partnership on research grants: A patient‐oriented research project	8
Youth engagement in mental health research: A systematic review	8
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	8
Refinement and Validation of a New Patient‐Reported Experience Measure for Hearing Loss (My Hearing PREM)	8
Preferences of patients with chronic low back pain about nonsurgical treatments: Results of a discrete choice experiment	8
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	8
Citizens' views on prices of medicines reimbursed by the National Health Service: Findings from Italian online focus groups	8
Priorities and preferences for care of people with multiple chronic conditions	8
Towards an Implementation‐STakeholder Engagement Model (I‐STEM) for improving health and social care services	8
Measuring Goal Progress Using the Goal‐Based Outcome Measure in Youth Wellness Hubs Ontario—An Integrated Youth Services Network	8
Developing a Consensus Statement to Target Oral Health Inequalities in People With Severe Mental Illness	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
Why do people choose not to take part in screening? Qualitative interview study of atrial fibrillation screening nonparticipation	8
Patient perceptions of in‐hospital laboratory blood testing: A patient‐oriented and patient co‐designed qualitative study	8
Issue Information	8
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Public perspectives on health improvement within a remote‐rural island community	8
Implementation of training to improve communication with disabled children on the ward: A feasibility study	8
Older Adults' Experiences and Expectations of Doctor–Patient Interactions During Early Hospital Care	8
A qualitative evaluation of a co‐design process involving young people at risk of suicide	8
Conceptualisations of positive mental health and wellbeing among children and adolescents in low‐ and middle‐income countries: A systematic review and narrative synthesis	8
Development of ACT+: A Novel, Person‐Centred Psychological Intervention Based on Acceptance and Commitment Therapy (ACT) to Improve Quality of Life in Patients Living With and Beyond Cancer	8
Conceptualizing patient participation in psychiatry: A survey describing the voice of patients in outpatient care	8
Barriers to accessing and receiving mental health care for paid and unpaid carers of older adults	8
Experiences of Home‐Based Pulmonary Rehabilitation With mHealth and Centre‐Based Pulmonary Rehabilitation in People With Chronic Obstructive Pulmonary Disease: A Qualitative Study	8
Patterns of Health Services and Medicine Utilisation by First‐Generation Pakistani Immigrants in New Zealand	7
Issue Information	7
The Challenging Process of Developing an Antenatal Social Intervention for Parents From Culturally Diverse Backgrounds to Reduce Postnatal Distress: A Participatory Action Research Study	7
Patient and public involvement in mental health research: En route to maturity?	7
‘“Health” Is Just One Piece in the Puzzle of Wellbeing’: Shifting From Preventing Health Deterioration to Improving Wellbeing in a Participatory Action Research Project With Care‐Experienced Older Peo	7
The elephant in the room: Family engagement in mental health and substance use research	7
Knowledge Families Hold: Co‐Production and Co‐Research With Mental Health Family Carers in Understanding Experiences During the COVID‐19 Pandemic	7
‘The Letter Says I May or May Not Be Eligible… It Is a Big Doubt and Frustrating:’ A Qualitative Study on Barriers and Facilitators to Children's Oral Healthcare From the Perspective of Karen Refugee	7
Identifying Key Moments in Type 2 Diabetes Management: A Qualitative Study of the Experiences of People With Type 2 Diabetes and Diabetes Health Coaches	7
Healthcare Professionals' Views on the Use of Passive Sensing and Machine Learning Approaches in Secondary Mental Healthcare: A Qualitative Study	7
Delivering the unexpected—Information needs for PSA screening from Men's perspective: A qualitative study	7
The development of a culturally sensitive educational video: How to facilitate informed decisions on cervical cancer screening among Turkish‐ and Moroccan‐Dutch women	7
Outcomes of importance to children and young adults with cerebral palsy, their parents and health professionals following lower limb orthopaedic surgery: A qualitative study to inform a Core Outcome S	7
How do Twitter users feel about telehealth? A mixed‐methods analysis of experiences, perceptions and expectations	7
Development of a User‐Centred Chronic Care Model for Patients With Heart Failure in a Limited‐Resource Setting: A Codesign Study	7
Issue Information	7
The World Café as a Tool for Evaluating the Level of Acceptance of SARS‐CoV‐2 Screening in School Settings, Puglia Region, Italy, 2023	7
Issue Information	7
Public Involvement to Enhance Care Home Research; Collaboration on a Minimum Data Set for Care Homes	7
The Baby Box scheme in Scotland: A study of public attitudes and social value	7
Supported Decision‐Making Interventions in Mental Healthcare: A Systematic Review of Evidence on the Outcomes for People With Mental Ill Health	7
Issue Information	7
Exploring Different Sampling Strategies: A Description of Our Success in Reaching Hard‐to‐Reach Turkish and Moroccan Immigrant Women in The Netherlands	7
Navigating HOPE (Hypermobile Online Pain managemEnt): Perspectives and Experiences From People With Hypermobile Ehlers–Danlos Syndrome or Hypermobility Spectrum Disorder on a Condition‐Specific Online	7
Acceptability of a standalone written leaflet for the National Health Service for England Targeted Lung Health Check Programme: A concurrent, think‐aloud study	7
Exploring patients' perspectives of gestational diabetes mellitus screening and counselling in Ontario: A grounded theory study	7
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Response to Comments on “Designing a Positive Health Dialogue Tool for Adolescents and Young Adults: A Mixed Methods Study”	7
Developing a community facilitator‐led participatory learning and action women's group intervention to improve infant feeding, care and dental hygiene practices in South Asian infants: NEON programme	7
Amplifying Women's Voices in Menopause Research: The Importance of Inclusive Perspectives	7
Ethical, legal, organizational and social issues related to the use of scalp cooling for the prevention of chemotherapy‐induced alopecia: A systematic review	7
Investigating the Factors Behind Patients' Desire and Decision to be Accompanied: A Cross‐Sectional Analysis	7
Patient and public involvement in the build‐up of COVID‐19 testing in Sweden	7
Exploring Adolescents' Understanding, Experiences and Beliefs About Pain: A Qualitative Study	7
Patient and public involvement and engagement with underserved communities in dementia research: Reporting on a partnership to co‐design a website for postdiagnostic dementia support	7
Agenda Setting in Outpatient Consultation of Older Adults With Long‐COVID	7
A Qualitative Exploration of the Role of Culturally Relevant Social Prescribing in Supporting Pakistani Carers Living in the UK	7
Issue Information	7
HIV Care Seeking Pathways and Barriers to the Continuum of Care Faced by Persons Living With HIV in Rural Nepal: A Qualitative Study	7
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Using World Cafés to engage an Australian culturally and linguistically diverse community around human papillomavirus vaccination	7
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Commissioning and co‐production in health and care services in the United Kingdom and Ireland: An exploratory literature review	6
‘No matter what time of day’: The value of joining Facebook groups supporting women's self‐management of gestational diabetes mellitus	6