Health Expectations

Article	Citations
Priorities and preferences for care of people with multiple chronic conditions	299
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	165
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	95
Co‐ideation and co‐design in co‐creation research: Reflections from the ‘Co‐Creating Safe Spaces’ project	66
The elephant in the room: Exploring the influence and participation of patients in infection‐related care across surgical pathways in South Africa and India	61
Pilot trial of iBDecide: Evaluating an online tool to facilitate shared decision making for adolescents and young adults with ulcerative colitis	57
The lived experience of weight loss maintenance in young people	57
Item development for a patient‐reported measure of compassionate healthcare in action	57
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	55
‘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	46
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	46
The Time Moving exhibit: Exploring perceptions of time in end‐of‐life experiences	45
‘You have to do what is best’: The lived reality of having a child who is repeatedly hospitalized because of acute lower respiratory infection	41
The Wellness Quest: A health literacy and self‐advocacy tool developed by youth for youth mental health	39
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	36
Public values to guide childhood vaccination mandates: A report on four Australian community juries	33
Creating safer cancer care with ethnic minority patients: A qualitative analysis of the experiences of cancer service staff	33
Indicators for adequate diabetes care for the indigenous communities of Ecuador	32
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The acceptability of, and informational needs related to, self‐collection cervical screening among women of Indian descent living in Victoria, Australia: A qualitative study	32
A public and patient consultation process as an aid to design a person‐centred randomized clinical trial	31
Inside Front Cover: Volume 25 Issue 1	31
Why do people choose not to take part in screening? Qualitative interview study of atrial fibrillation screening nonparticipation	31
Barriers to preventive care utilization among Hong Kong community‐dwelling older people and their views on using financial incentives to improve preventive care utilization	31
Issue Information	29

Issue Information	29
Exploring COVID‐19 experiences for persons with multiple sclerosis and carers: An Australian qualitative study	25
Identifying locally actionable strategies to increase participant acceptability and feasibility to participate in Phase I cancer clinical trials	25
A patient‐led, peer‐to‐peer qualitative study on the psychosocial relationship between young adults with inflammatory bowel disease and food	25
Pathways to recovery model of youth substance misuse in Assam, India	24
Patient research priority setting partnership in human T‐cell lymphotropic virus type I	22
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	21
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	21
Awareness of diagnosis, treatment and risk of late effects in Chinese survivors of childhood cancer in Hong Kong	21
Reimagining consumer involvement: Resilient system indicators in the COVID‐19 pandemic response in New South Wales, Australia	21
A qualitative exploration of the barriers and facilitators affecting ethnic minority patient groups when accessing medicine review services: Perspectives of healthcare professionals	20
Issue Information	20
Barriers and facilitators to mobile health and active surveillance use among older adults with skin disease	20
Experiences and perceptions of continuous deep sedation: An interview study among Dutch patients and relatives	20
The impact of expert by experience involvement in teaching in a DClinPsych programme; for trainees and experts by experience	20
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	20
Involving people with type 2 diabetes in facilitating participation in a cardiovascular screening programme	20
Exploring the barriers and facilitators to volunteering as an intervention for those with long‐term neurological conditions: How make therapeutic volunteering possible?	19
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	19
Exploring the experiences and preferences of South Asian patients' of primary care in England since COVID‐19	18
Patient preferences for heart valve disease intervention	18
‘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	18
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	18
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	18
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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	17
Barriers to accessing and receiving mental health care for paid and unpaid carers of older adults	17
Shaping research for people living with co‐existing mental and physical health conditions: A research priority setting initiative from the United Kingdom	17
Experiences of people with Long Covid with a digital physiotherapy intervention: A qualitative study	17
Management of COVID‐19 and vaccination in Nepal: A qualitative study	16
A co‐created multimethod evaluation of recovery education in Ireland	16
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Feasibility of a best–worst scaling exercise to set priorities for autism research	16
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	15
How Do Australians Manage Diagnostic Testing Risks? Focus Groups Linked to a Model of Behaviour Change	15
Evaluating Experiences in a Digital Nutrition Education Program for People With Multiple Sclerosis: A Qualitative Study	15
Exploring General Practitioners' Management of Self‐Harm in Young People: A Qualitative Study	15
Transitions: Living With Young‐Onset Alzheimer's Disease: A Qualitative Interview Study	15
Letter to the Editor: Best Practices on Public and Patient Involvement in Interprofessional Healthcare Education	15
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	15
Impact of Interventions on Medication Adherence in Patients With Coexisting Diabetes and Hypertension	15
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	15
Building Relationships, Forming Collaborations: Lessons Learned From an Unconference Seeking to Cultivate Solutions in Healthcare	15
‘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	14
(Dis)trust in doctors and public and private healthcare institutions in the Western Balkans	14
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	14
The Dilemmas and Opportunities of Co‐Creating Health Interventions to Fit Local Contexts: An Ethnographic Study on the Adaptation of Clinical Guidelines in Tanzania	14
What are the views of three key stakeholder groups on extending the breast screening interval for low‐risk women? A secondary qualitative analysis	14
Issue Information	14
Exploring Healthcare Paradoxes in Hospital Haemodialysis—A Qualitative Study	14

Evaluating the benefit of early patient and public involvement for product development and testing with small companies	14
Sexual Interventions in the Metaverse: Attitudes Towards Novel Therapeutic Approaches, a Qualitative Study	14
Perceptions of recovery and rehabilitation in people with brain injury in Spain. A qualitative study	13
The development of PAT‐HD: A co‐designed tool to promote physical activity in people with Huntington’s disease	13
My Wellbeing Journal: Development of a communication and goal‐setting tool to improve care for older adults with chronic conditions and multimorbidity	13
Children's perspectives and experiences of the COVID‐19 pandemic and UK public health measures	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
Self‐management interventions for children and young people with sickle cell disease: A systematic review	13
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	13
Using financial incentives to support service engagement of adults experiencing homelessness and mental illness: A qualitative analysis of key stakeholder perspectives	13
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	13
‘It reshaped how I will do research’: A qualitative exploration of team members’ experiences with youth and family engagement in a randomized controlled trial	13
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	13
Adapting patient and public involvement in patient‐oriented methods research: Reflections in a Canadian setting during COVID‐19	13
Patients' experiences of behaviour change interventions delivered by general practitioners during routine consultations: A nationally representative survey	13
Development and psychometric testing of the patient participation in bedside handover survey	12
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	12
Sociocultural influences on asthma self‐management in a multicultural society: A qualitative study amongst Malaysian adults	12
The psychological consequences of living with coronary heart disease: Are patients' psychological needs served? A mixed‐method study in Germany	12
Exploring first‐time mothers' experiences and knowledge about behavioural risk factors for stillbirth	12
‘A good decision is the one that feels right for me’: Codesign with patients to inform theoretical underpinning of a decision aid website	12
Experiences of human papillomavirus self‐sampling by women >60 years old: A qualitative study	12
Operationalizing a patient engagement plan for health research: Sharing a codesigned planning template from a national clinical trial	12
Optimizing the implementation of lung cancer screening in Scotland: Focus group participant perspectives in the LUNGSCOT study	11
A qualitative evaluation of a co‐design process involving young people at risk of suicide	11
Reflections from the COVID‐19 pandemic on inequalities and patient and public involvement and engagement (PPIE) in social care, health and public health research	11
Developing a Consensus Statement to Target Oral Health Inequalities in People With Severe Mental Illness	11
Lived experience engagement in mental health research: Recommendations for a terminology shift	11
A challenge in qualitative research: Family members sitting in on interviews about sensitive subjects	11
Participatory Design in Suicide Prevention: A Qualitative Study of International Students' Experiences of Adapting the LivingWorks safeTALK Programme	11
Conceptualizing patient participation in psychiatry: A survey describing the voice of patients in outpatient care	11
The Mediating Role of Students' Health Information Literacy Skills: Exploring the Relationship Between Web Resource Utilization and Health Information Evaluation Proficiency	11
Sharing administrative health data with private industry: A report on two citizens' juries	11
‘None of Them Know Me’: A Qualitative Study of the Implications of Locum Doctor Working for Patient Experience	11
Perceptions of the Impact of Comorbidity on the Bowel Cancer Screening Programme: Qualitative Study With Bowel Screening Participants and Staff	10
‘It's Just Not Working’, a Qualitative Exploration of the Weight‐Related Healthcare Experiences of Individuals of Arab Heritage With Higher Weight in Australia	10
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	10
Perspectives of women living with type 1 diabetes regarding preconception and antenatal care: A qualitative evidence synthesis	10
A Qualitative Exploration of Stroke Survivors' Experiences of Using a Stroke Helpline	10
Partnered Recruitment: Engaging Individuals With Lived Experience in the Recruitment of Co‐Design Participants	10
Developing the Resident Measure of Safety in Care Homes (RMOS): A Delphi and Think Aloud Study	10
A Socioecological Approach to Support the Transition to Adult Care for Youth With Medical Complexity: Family Perspectives and Recommendations	10
Patients', carers' and healthcare providers' views of patient‐held health records in Kerala, India: A qualitative exploratory study	10
‘The Norm Is to Not Openly Collaborate’: Using the Lens of Co‐Production to Evaluate the Development of a COVID‐19 ICU Triage Policy	10
Public Perceptions of the Australian Health System During COVID‐19: Findings From a 2021 Survey Compared to Four Previous Surveys	10
Information, deliberation, and decisional control preferences for participation in medical decision‐making and its influencing factors among Chinese cancer patients	10
Co‐building a training programme to facilitate patient, family and community partnership on research grants: A patient‐oriented research project	10
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Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	9
The psychosocial impact of a chronic disease in Ireland: Burdens and helpful practices for a life with epidermolysis bullosa	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
A Decision Aid for Patients Considering Surgery for Sciatica: Codesign and User‐Testing With Patients and Clinicians	9
Development and validation of educational multimedia to promote public health literacy about healthy cognitive aging	9
Evaluating the effectiveness of the Family Connections program for caregivers of youth with mental health challenges, part I: A quantitative analysis	9
From Polarity to Plurality: Perceptions of COVID‐19 and Policy Measures in England and Scotland	9
Different views on collaboration between older persons, informal caregivers and care professionals	9
Conceptual and practical challenges associated with understanding patient safety within community‐based mental health services	9
Towards understanding and improving medication safety for patients with mental illness in primary care: A multimethod study	9
Rationalizing the Influence of Co‐Design on Distress, Clinical Decision‐Making and Disease Self‐Management of Cancer Patients‐as‐Partners: A Quasi‐Experimental Study	9
Just a story? Leadership, lived experience and integrated care	9
Recovery in Mind: A Recovery College's journey through the Covid‐19 pandemic	9
Understanding and Defining Young People's Involvement and Under‐Representation in Mental Health Research: A Delphi Study	9
Value in care: The contribution of supportive care to value‐based lung cancer services—A qualitative semistructured interview study	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
Barriers and facilitators of shared decision making in acutely ill inpatients with schizophrenia—Qualitative findings from the intervention group of a randomised‐controlled trial	9
Embedding Public Involvement in a PhD Research Project With People Affected by Advanced Liver Disease	9
What aspects of health and wellbeing are most important to parent carers of children with disabilities?	9
Conceptualisations of positive mental health and wellbeing among children and adolescents in low‐ and middle‐income countries: A systematic review and narrative synthesis	9
Exploring the sources of cervical cancer screening self‐efficacy among rural females: A qualitative study	9
How is patient‐centred care conceptualized in obstetrical health? comparison of themes from concept analyses in obstetrical health‐ and patient‐centred care	8
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	8
Meaningful engagement through critical reflexivity: Engaging people with lived experience in continuing mental health professional development	8
Engaging with Culturally and Linguistically Diverse Communities to Promote Palliative Care That Exceeds Expectation	8
Delivery of Supported Self‐Management in Primary Care Asthma Reviews: Insights From the IMP2ART Programme	8
Cancer survival stories: Perception, creation, and potential use case	8
Coproduction of a resource sharing public views of health inequalities: An example of inclusive public and patient involvement and engagement	8
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	8
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	8

Healthcare Professionals' Responses to Complaints: A Qualitative Interview Study With Patients, Carers and Healthcare Professionals Using the Theoretical Domains Framework and COM‐B Model	8
Validating care and treatment scenarios for measuring decisional conflict regarding future care preferences among older adults	8
What really is nontokenistic fully inclusive patient and public involvement/engagement in research?	8
What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability	8
Evaluation of patient engagement in medicine development: A multi‐stakeholder framework with metrics	8
Community‐Driven Health Promotion: Evaluation of a Rural Microgrant Program	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
Participatory research with carers: A systematic review and narrative synthesis	8
Towards an Implementation‐STakeholder Engagement Model (I‐STEM) for improving health and social care services	8
“I would not go to him”: Focus groups exploring community responses to a public health campaign aimed at reducing unnecessary diagnostic imaging of low back pain	8
Lived Experience and Family Engagement in Mental Health and Substance use Health Research: Case Profiles of Five Studies	8
Stakeholder perspectives on the implementation and impact of Indigenous health interventions: A systematic review of qualitative studies	8
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	8
Youth engagement in mental health research: A systematic review	8
“After Cutting It, Things Have Never Remained the Same”: A Qualitative Study of the Perspectives of Amputees and Their Caregivers	8
Engagement With Professional Stakeholders in Healthcare Research—The Case of the Dementia PersonAlised Care Team (D‐PACT) Project in the United Kingdom	8
‘Advocacy groups are the connectors’: Experiences and contributions of rare disease patient organization leaders in advanced neurotherapeutics	8
Supporting the involvement of older adults with complex needs in evaluation of outcomes in long‐term care at home programmes	8
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	8
Engaging veteran stakeholders to identify patient‐centred research priorities for optimizing implementation of lung cancer screening	8
Community Preferences for Allied Health Services in Residential Aged Care	8
Conceptualization of patient‐centered care in Latin America: A scoping review	7
‘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	7
How and why do doctors communicate diagnostic uncertainty: An experimental vignette study	7
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	7
Haemochromatosis patients' research priorities: Towards an improved quality of life	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
Mindfulness for people with chronic pain: Factors affecting engagement and suggestions for programme optimisation	7
Implementation of training to improve communication with disabled children on the ward: A feasibility study	7
Issue Information	7
Erratum to: “The Bidirectional Engagement and Equity (BEE) Research Framework to Guide Community‐Academic Partnerships: Developed From a Narrative Review and Diverse Stakeholder Perspectives”	7
The experience of shared decision‐making for people with asthma: A systematic review and metasynthesis of qualitative studies	7
Corrigendum	7
Knowledge sharing to support long‐term condition self‐management—Patient and health‐care professional perspectives	7
Prioritizing Chinese medicine clinical research questions in cancer palliative care from patient and caregiver perspectives	7
Family carers' experiences and perceived roles in interprofessional collaborative practice in primary care: A constructivist grounded theory study	7
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	7
‘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	7
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Telehealth in a paediatric developmental metropolitan assessment clinic: Perspectives and experiences of families and clinicians	7
Viewpoints among experts and the public in the Netherlands on including a lifestyle criterion in the healthcare priority setting	7
‘Physical well‐being is our top priority’: Healthcare professionals' challenges in supporting psychosocial well‐being in stroke services	7
Amplifying Women's Voices in Menopause Research: The Importance of Inclusive Perspectives	7
Exploring adolescents' experiences of continuing to wear face masks during COVID‐19: A qualitative descriptive study in Barcelona (Spain)	7
Applying self‐determination theory towards motivational factors of physical activity in people undergoing haemodialyses: A qualitative interview study	7
Citizens' views on prices of medicines reimbursed by the National Health Service: Findings from Italian online focus groups	7
Erratum	7
A mapping and synthesis of tools for stakeholder and community engagement in quality improvement initiatives for reproductive, maternal, newborn, child and adolescent health	7
Patient and general practitioner experiences of implementing a medication review intervention in older people with multimorbidity: Process evaluation of the SPPiRE trial	7
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs	7
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	7
Insights and recommendations for working collaboratively and improving care in Alzheimer's disease: Learnings from the Finding Alzheimer's Solutions Together (F.A.S.T.) Council	7
Emotion in public involvement: A conceptual review	7
Needs assessment for health service design for people with back pain in a hospital setting: A qualitative study	7
Patient and public involvement in mental health research: En route to maturity?	7
Expectations of a new opt‐out system of consent for deceased organ donation in England: A qualitative interview study	7
Preference‐based patient participation for most, if not all: A cross‐sectional study of patient participation amongst persons with end‐stage kidney disease	7
Exploring the lived experience of receiving mental health crisis care at emergency departments, crisis phone lines and crisis care alternatives	7
Correction to ‘Optimizing the design and implementation of question prompt lists to support person‐centred care: A scoping review’	7
Preferences of patients with chronic low back pain about nonsurgical treatments: Results of a discrete choice experiment	7
Rapid development of a COVID‐19 care planning decision‐aid for family carers of people living with dementia	7
Factors explaining the fear of being infected with COVID‐19	6
The dynamic nature of patient engagement within a Canadian patient‐oriented kidney health research network: Perspectives of researchers and patient partners	6
Evaluating the effectiveness of the Family Connections program for caregivers of youth with mental health challenges, part II: A qualitative analysis	6
The experiences of psychiatric patients, their caregivers and companions in upholding patient dignity during hospitalization: A qualitative study	6
Communication strategies to encourage child participation in an oral health promotion session: An exemplar video observational study	6
Unpacking the potential of developmental evaluation in codesign work	6
Experiences and expectations of receiving volunteer services among home‐based elderly in Chinese urban areas: A qualitative study	6
Transitional care decision‐making through the eyes of older people and informal caregivers: An in‐depth interview‐based study	6
Young adults' healthcare utilisation and healthcare needs: Perceptions and experiences of healthcare providers	6
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Self‐directed self‐management interventions to prevent or address distress in young people with long‐term physical conditions: A rapid review	6
Issue Information	6
‘Opportunity to bond and a sense of normality’: Parent and staff views of cuddling babies undergoing therapeutic hypothermia in neonatal intensive care: ‘CoolCuddle’	6
Emergency department patient‐centred care perspectives from deaf and hard‐of‐hearing patients	6
Acceptability of a standalone written leaflet for the National Health Service for England Targeted Lung Health Check Programme: A concurrent, think‐aloud study	6
Patient engagement in care: A scoping review of recently validated tools assessing patients' and healthcare professionals' preferences and experience	6
Popular science and education of cosmetic surgery in China: Quality and reliability evaluation of Douyin short videos	6
Exploring patients' perspectives of gestational diabetes mellitus screening and counselling in Ontario: A grounded theory study	6
Patient views on asthma diagnosis and how a clinical decision support system could help: A qualitative study	6
‘Keeping it real’: A qualitative exploration of preferences of people with lived experience for participation and active involvement in mental health research in Australia	6
Content validity testing of the INTERMED Self‐Assessment in a sample of adults with rheumatoid arthritis and rheumatology healthcare providers	6
Issue Information	6
‘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	6
Assessment of medication adherence, medication safety awareness and medication practice among patients with lung cancer: A multicentre cross‐sectional study	6
Patient and public involvement in the build‐up of COVID‐19 testing in Sweden	6
‘We have goals but [it is difficult]’. Barriers to antiretroviral therapy adherence among women using alcohol and other drugs living with HIV in South Africa	6
Access and communication for deaf individuals in Australian primary care	6
Do patient engagement interventions work for all patients? A systematic review and realist synthesis of interventions to enhance patient safety	6
Person‐centred caregiver singing for people living with dementia in South Africa: A mixed methods evaluation of acceptability, feasibility, and professional caregivers' experiences	6
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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	6
Physicians' perceptions of patient participation and the involvement of family caregivers in the palliative care pathway	6
“Whilst you are here…” Acceptability of providing advice about screening and early detection of other cancers as part of the breast cancer screening programme	6
My child is growing and now? Exploring the environmental needs of children with congenital Zika syndrome according to their caregivers' perceptions	6