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1. A qualitative exploration of the barriers and facilitators to self‐managing multiple long‐term conditions amongst people experiencing socioeconomic deprivation.

2. Shaping research for people living with co‐existing mental and physical health conditions: A research priority setting initiative from the United Kingdom.

3. A co‐created multimethod evaluation of recovery education in Ireland.

4. Towards an Implementation‐STakeholder Engagement Model (I‐STEM) for improving health and social care services.

5. Experiences of health service access: A qualitative interview study of people living with Parkinson's disease in Ireland.

6. Who cares for the carer? Codesigning a carer health and wellbeing clinic for older care partners of older people in Australia.

7. Acceptability of a shared cancer follow‐up model of care between general practitioners and radiation oncologists: A qualitative evaluation.

8. 'To me, it's ones and zeros, but in reality that one is death': A qualitative study exploring researchers' experience of involving and engaging seldom‐heard communities in big data research.

9. Developing a Health Literacy Scale for adults in Hong Kong: A modified e‐Delphi study with healthcare consumers and providers.

10. The interactive dimensions of encounters in HIV care: From trauma to relational traumatic growth.

11. Exploring the obesity concerns of British Pakistani women living in deprived inner‐city areas: A qualitative study.

12. Attribute nonattendance in COVID‐19 vaccine choice: A discrete choice experiment based on Chinese public preference.

13. Intertwined like a double helix: A meta‐synthesis of the qualitative literature examining the experiences of living with someone with multiple sclerosis.

14. The lived experience of a novel disruptive therapy in a group of men and boys with haemophilia A with inhibitors: Emi & Me.

15. Living with epidermolysis bullosa: Daily challenges and health‐care needs.

16. Reluctant educators and self‐advocates: Older trans adults' experiences of health‐care services and practitioners in seeking gender‐affirming services.

17. Women's and peer supporters' experiences of an assets‐based peer support intervention for increasing breastfeeding initiation and continuation: A qualitative study.

18. Patients' perceptions of their doctors' notes and after‐visit summaries: A mixed methods study of patients at safety‐net clinics.

19. Decision making in NICE single technological appraisals: How does NICE incorporate patient perspectives?

20. PReSaFe: A model of barriers and facilitators to patients providing feedback on experiences of safety.