OOIR: Observatory of International Research

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 2020-10-01 to 2024-10-01.)

Article	Citations
Patient‐reported outcome measures (PROMs): A review of generic and condition‐specific measures and a discussion of trends and issues	258
Understanding COVID‐19 misinformation and vaccine hesitancy in context: Findings from a qualitative study involving citizens in Bradford, UK	165
Public preference for COVID‐19 vaccines in China: A discrete choice experiment	110
Mapping definitions of co‐production and co‐design in health and social care: A systematic scoping review providing lessons for the future	95
Public attitudes towards COVID‐19 contact tracing apps: A UK‐based focus group study	85
Patients as partners in health research: A scoping review	62
Pragmatism as a paradigm for patient‐oriented research	61
The psychological burden of waiting for procedures and patient‐centred strategies that could support the mental health of wait‐listed patients and caregivers during the COVID‐19 pandemic: A scoping re	57
Factors explaining the fear of being infected with COVID‐19	57
'Reluctant pioneer': A qualitative study of doctors' experiences as patients with long COVID	57
The ultimate question? Evaluating the use of Net Promoter Score in healthcare: A systematic review	46
Meaningful patient and public involvement in digital health innovation, implementation and evaluation: A systematic review	44
Mitigating unintended consequences of co‐design in health care	42
Mediated roles of generalized trust and perceived social support in the effects of problematic social media use on mental health: A cross‐sectional study	42
Youth engagement in mental health research: A systematic review	41
Exploring invisibility and epistemic injustice in Long Covid—A citizen science qualitative analysis of patient stories from an online Covid community	39
‘I don't know what to do or where to go’. Experiences of accessing healthcare support from the perspectives of people living with Long Covid and healthcare professionals: A qualitative study in Bradfo	36
How different health literacy dimensions influences health and well‐being among men and women: The mediating role of health behaviours	36
Trust, medical expertise and humaneness: A qualitative study on people with cancer’ satisfaction with medical care	33
Do patient engagement interventions work for all patients? A systematic review and realist synthesis of interventions to enhance patient safety	33
‘Imposter participants’ in online qualitative research, a new and increasing threat to data integrity?	32
Ensuring patient and public involvement in the transition to AI‐assisted mental health care: A systematic scoping review and agenda for design justice	32
Participatory health research with migrants: Opportunities, challenges, and way forwards	31
Shortening and validation of the Patient Engagement In Research Scale (PEIRS) for measuring meaningful patient and family caregiver engagement	31
The manifestation of participation within a co‐design process involving patients, significant others and health‐care professionals	29

Towards conceptual convergence: A systematic review of psychological resilience in family caregivers of persons living with chronic neurological conditions	29
A scoping review of practice recommendations for clinicians’ communication of uncertainty	29
Determinants of patient activation and its association with cardiovascular disease risk in chronic kidney disease: A cross‐sectional study	29