Health Expectations

Papers
(The H4-Index of Health Expectations is 28. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-11-01 to 2025-11-01.)
ArticleCitations
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study178
Feasibility of a best–worst scaling exercise to set priorities for autism research138
100
Just a story? Leadership, lived experience and integrated care98
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ93
Community views on the secondary use of general practice data: Findings from a mixed‐methods study87
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark71
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders67
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 programme66
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study54
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life50
Identification and Applications of Key Elements in the Development of Pictorial Support for People With Aphasia After Stroke: A Co‐Design Approach42
Continuity Is Essential: The Experiences of Co‐Design Participants During the Implementation of a New Health Service40
Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey39
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition38
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers38
Youth engagement in mental health research: A systematic review35
Children's Communication Choices About Musculoskeletal Pain and Injury: Insights From a Public Involvement Event35
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review34
Participatory research with carers: A systematic review and narrative synthesis34
Identifying Common Patient‐Oriented Priorities for Child and Adolescent Health Research and Care: A Systematic Review of Priority Setting Partnerships34
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs33
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions32
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice32
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff31
Indicators for adequate diabetes care for the indigenous communities of Ecuador30
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage29
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 3–1329
Developing a novel co‐produced methodology to understand ‘real‐world’ help‐seeking in online peer–peer communities by young people experiencing emotional abuse and neglect28
Inside Front Cover: Volume 25 Issue 128
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs28
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study28
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