Health Expectations: Vol 24, No 4

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Health Expectations: Volume 24, Issue 4

ISSUE INFORMATION

Issue Information

REVIEW ARTICLES

Patient-reported outcome measures (PROMs): A review of generic and condition-specific measures and a discussion of trends and issues

A scoping review of practice recommendations for clinicians’ communication of uncertainty

Adolescent and young adult patients as co-researchers: A scoping review

Correction(s) for this article

Corrigendum

Patient partners’ perspectives of meaningful engagement in synthesis reviews: A patient-oriented rapid review

Ensuring patient and public involvement in the transition to AI-assisted mental health care: A systematic scoping review and agenda for design justice

ORIGINAL ARTICLES

Developing and user testing new pharmacy label formats—A study to inform labelling standards

Talk to us! Communication is a key factor in improving the comfort of MRI research participants

A nationwide participatory programme to measure person-centred hospital care in Italy: Results and implications for continuous improvement

Understanding COVID-19 misinformation and vaccine hesitancy in context: Findings from a qualitative study involving citizens in Bradford, UK

Patient perspectives on quality of care for depression and anxiety in primary health care teams: A qualitative study

Processes for evidence summarization for patient decision aids: A Delphi consensus study

Dissonance in the discourse of the duration of diabetes: A mixed methods study of patient perceptions and clinical practice

Patient representatives: Crucial members of health-care working groups facing an uncertain role and conflicting expectations. A qualitative study

Digital reminiscence app co-created by people living with dementia and carers: Usability and eye gaze analysis

Participatory design and qualitative evaluation of a decision guide for workplace human immunodeficiency virus self-disclosure: The importance of a socio-ecological perspective

Assessing and promoting partnership between patients and health-care professionals: Co-construction of the CADICEE tool for patients and their relatives

Barriers to preventive care utilization among Hong Kong community-dwelling older people and their views on using financial incentives to improve preventive care utilization

Patients as qualitative data analysts: Developing a method for a process evaluation of the ‘Improving the Safety and Continuity of Medicines management at care Transitions’ (ISCOMAT) cluster randomised control trial

Long-term consumer involvement in cancer research: Working towards partnership

‘Birthing a Better Future’: A mixed-methods evaluation of an exhibition on the early years of life

Public perspectives on health improvement within a remote-rural island community

Priorities and preferences for care of people with multiple chronic conditions

Advance care directive prevalence among older Australians and associations with person-level predictors and quality indicators

Acceptability of risk-stratified population screening across cancer types: Qualitative interviews with the Australian public

Sharing administrative health data with private industry: A report on two citizens' juries

Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation

A qualitative study of nurse-patient communication and information provision during surgical pre-admission clinics

Health-care professionals’ assessment of a person-centred intervention to empower self-management and health across chronic illness: Qualitative findings from a process evaluation study

Patients as partners in health research: A scoping review

Patient perspectives on the need for implanted device information: Implications for a post-procedural communication framework

Delivering the unexpected—Information needs for PSA screening from Men's perspective: A qualitative study

More than cost-effectiveness? Applying a second-stage filter to improve policy decision making

User involvement in the making: Positions and types of knowledge enacted in the interaction between service users and researchers in user panel meetings

Implementation of training to improve communication with disabled children on the ward: A feasibility study

Conceptualizing patient participation in psychiatry: A survey describing the voice of patients in outpatient care

A Community Jury on initiating weight management conversations in primary care

Experiences of cervical screening participation and non-participation in women from minority ethnic populations in Scotland

Awareness of diagnosis, treatment and risk of late effects in Chinese survivors of childhood cancer in Hong Kong

Prioritizing Chinese medicine clinical research questions in cancer palliative care from patient and caregiver perspectives

An intervention of sustainable weight change: Influence of self-help group and expectations

‘I hated being ghosted’ – The relevance of social participation for living well with post-stroke aphasia: Qualitative interviews with working aged adults

Improving the depth of data quality or increasing confusion? Reflections on a data analysis involving members of a self-help group for relatives of people living with dementia

Assessing people with dementia participating in cognitive stimulation activities—A qualitative pilot video analysis exploring the importance of facilitating the participation

Understanding young adults’ reasons for seeking ‘clinically unnecessary’ urgent and emergency care: A qualitative interview study

LETTER TO THE EDITOR

A challenge in qualitative research: Family members sitting in on interviews about sensitive subjects

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