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1. Rethinking 'need' for clinical support in transgender and gender non‐conforming children without clinical classification: Learning from 'the paper I almost wrote'.

3. Exploring Whether and How People Experiencing High Deprivation Access Diagnostic Services: A Qualitative Systematic Review.

4. Rabies control in Ghana: Stakeholders interventions, challenges and opportunities.

5. Consultations With Muslims From Minoritised Ethnic Communities Living in Deprived Areas: Identifying Inequities in Mental Health Care and Support.

6. Editorial: The American College of Rheumatology White Paper on Biosimilars: It Isn't All White—There Is Some Gray and Black.

7. Being a patient among other patients: Refugees' political inclusion through the Austrian solidarity‐based healthcare system.

8. Parenting through place‐of‐care disruptions: A qualitative study of parents' experiences of neonatal care.

9. Youth Perspectives on 'Highly Personalised and Measurement‐Based Care': Qualitative Co‐Design of Education Materials.

10. "Will you need this health at all? Will you be alive?": using the bioecological model of mass trauma to understand HIV care experiences during the war in Ukraine.

11. The psychosocial impact of a chronic disease in Ireland: Burdens and helpful practices for a life with epidermolysis bullosa.

12. Conceptualising community engagement as an infinite game implemented through finite games of 'research', 'community organising' and 'knowledge mobilisation'.

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

15. Nursing privilege: A concept analysis.

16. A qualitative study assessing allied health provider perceptions of telepractice functionality in therapy delivery for people with disability.

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

18. Amplifying the voices of Black racial minorities in mental health research through public involvement and engagement: The importance of advisory roles.

19. Co‐designing a theory‐informed, multicomponent intervention to increase vaccine uptake with Congolese migrants: A qualitative, community‐based participatory research study (LISOLO MALAMU).

20. Antenatal care and skilled delivery service utilisation in Somali pastoral communities of Eastern Ethiopia

21. Stories for Change: The impact of Public Narrative on the co‐production process.

22. Social determinants of health for children with cerebral palsy and their families.

23. Advancing nursing practice with artificial intelligence: Enhancing preparedness for the future.

24. The role of payment and financing in achieving health equity.

25. Implementing patient–public engagement for improved health: Lessons from three Ghanaian community‐based programmes.

26. Religious accommodation, agonism, agnosticism in healthcare: A commentary on Joshua Hordern, 'Accommodating religion and belief in healthcare: Political threats, agonistic democracy and established religion'.

27. "Autonomy and solidarity: Bridging the tensions": Celebrating the 15th World Congress of Bioethics.

28. Network‐building by community actors to develop capacities for coproduction of health services following reforms: A case study.

29. Addressing social inequity through improving relational care: A social–ecological model based on the experiences of migrant women and midwives in South Wales.

30. Measure of accessibility to postal services in France: A potential spatial accessibility approach applied in an urban region.

31. Equality‐enhancing potential of novel forms of assisted gestation: Perspectives of reproductive rights advocates.

32. Iwinac 2017: Assistive intelligence for the elderly.

33. 'Mad', bad or Muslim? The UK's Vulnerability Support Hubs and the nexus of mental health, counterterrorism and racism.

34. Rethinking the issue of reparations for Black Americans.

35. Pathways to well‐being in Tarumajaya, West Java: Post‐COVID 19 supporting better access to the commons through engagement and a critical systemic reflection on stories.

36. The location of urban healthcare services: Evidence from Phoenix Yelp reviews.

37. Patient public involvement (PPI) in health literacy research: Engagement of adults with literacy needs in the co‐creation of a hospital‐based health literacy plan.

38. Nutrition in Nepal: Three decades of commitment to children and women.

39. Monitoring and modifying recruitment and retention strategies for an ongoing randomised clinical trial with venous leg ulcer patients: Overcoming barriers to participation.

40. Access to effective but expensive treatments: An analysis of the solidarity argument in discussions on funding of medical treatments.

41. Inside, outside and in‐between: The process and impact of co‐producing knowledge about autism in a UK Somali community.

42. Perceptions and experiences of diabetic foot ulceration and foot care in people with diabetes: A qualitative meta‐synthesis.

43. International Collaboration to Ensure Equitable Access to Vaccines for COVID‐19: The ACT‐Accelerator and the COVAX Facility.

44. When women win, we all win—Call for a gendered global NCD agenda.

45. Barriers of and strategies for shared decision‐making implementation in the care of metastatic breast cancer: A qualitative study among patients and healthcare professionals in an Asian country.

46. Post‐Roe emergency medicine: Policy, clinical, training, and individual implications for emergency clinicians.

47. Withdrawal of intensive care during times of severe scarcity: Triage during a pandemic only upon arrival or with the inclusion of patients who are already under treatment?

48. Programmatic adaptations to acute malnutrition screening and treatment during the COVID‐19 pandemic.

49. Similar values, different expectations: How do patients and providers view 'health' and perceive the healthcare experience?

50. Parents’ views on how health professionals should work with them now to get the best for their child in the future