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1. Patient‐Led Research to Develop a Training Programme for Restoring Musical Joy in Cochlear Implant Recipients: A Reflexive Process Evaluation.

2. 'Talking the talk or walking the walk?' A bibliometric review of the literature on public involvement in health research published between 1995 and 2009.

3. Pathways for Strengthening Lived Experience Leadership for Transformative Systems Change: Reflections on Research and Collective Change Strategies.

4. Strengthening mental health research outcomes through genuine partnerships with young people with lived or living experience: A pilot evaluation study.

5. Public perspectives on inequality and mental health: A peer research study.

6. Guiding, sustaining and growing the public involvement of young people in an adolescent health research community of practice.

7. Community Engagement in a complex intervention to improve access to primary mental health care for hard-to-reach groups

8. User involvement in long-term care. Towards a relational care-ethics approach

9. Participatory codesign of patient involvement in a Learning Health System: How can data‐driven care be patient‐driven care?

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

11. Patient‐Led Research to Develop a Training Programme for Restoring Musical Joy in Cochlear Implant Recipients: A Reflexive Process Evaluation

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

13. Ethical issues in participatory arts methods for young people with adverse childhood experiences.

14. Using World Cafés to engage an Australian culturally and linguistically diverse community around human papillomavirus vaccination.

15. Research and recovery: Can patient participation in research promote recovery for people with complex post‐traumatic stress disorder, CPTSD?

16. Measuring the impact of participatory research in psychiatry: How the search for epistemic justifications obscures ethical considerations.

17. Translating new science into the community to promote opportunities for breast and cervical cancer prevention among African American women.

18. The Dilemmas and Opportunities of Co‐Creating Health Interventions to Fit Local Contexts: An Ethnographic Study on the Adaptation of Clinical Guidelines in Tanzania.

19. Professionals' Perceptions of the Colorectal Cancer Pathway: Results of a Co‐Constructed Qualitative Study.

20. Reflections on the opportunities and challenges of applying experience‐based co‐design (EBCD) to phase 1 clinical trials in oncology.

21. Experiences of Living With the Nonmotor Symptoms of Parkinson's Disease: A Photovoice Study.

22. Engaging women to set the research agenda for assisted vaginal birth.

23. Disrupting patterns of exclusion in participatory spaces: Involving people from vulnerable populations.

24. Patient and public involvement in the development of health services: Engagement of underserved populations in a quality improvement programme for inflammatory bowel disease using a community‐based participatory approach.

25. Community Engagement in a complex intervention to improve access to primary mental health care for hard-to-reach groups.

26. Implementing peer support work in mental health care in Germany: The methodological framework of the collaborative, participatory, mixed‐methods study (ImpPeer‐Psy5).

27. Development of an information source for patients and the public about general practice services: an action research study.

28. Environmental health perceptions of urban youth from low‐income communities: A qualitative photovoice study and framework.

29. Material practices for meaningful engagement: An analysis of participatory learning and action research techniques for data generation and analysis in a health research partnership.

30. Co‐ideation and co‐design in co‐creation research: Reflections from the 'Co‐Creating Safe Spaces' project.

31. Use of co‐design methodology in the development of cardiovascular disease secondary prevention interventions: A scoping review.

32. Adapting a codesign process with young people to prioritize outcomes for a systematic review of interventions to prevent self‐harm and suicide.

33. Codesigning a patient support portal with health professionals and men with prostate cancer: An action research study.

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

35. The manifestation of participation within a co‐design process involving patients, significant others and health‐care professionals.

36. Patient involvement in developing a patient‐targeted feedback intervention after depression screening in primary care within the randomized controlled trial GET.FEEDBACK.GP.

37. Evaluation of patient engagement in medicine development: A multi‐stakeholder framework with metrics.

38. Stakeholder engagement from problem analysis to implementation strategies for a patient‐reported experience measure in disability care: A qualitative study on the process and experiences.

39. Facilitating personal development for public involvement in health‐care education and research: A co‐produced pilot study in one UK higher education institute.

40. The potential for coproduction to add value to research.

41. Research and knowledge transfer priorities in developmental coordination disorder: Results from consultations with multiple stakeholders.

42. Mindfulness‐based practices with family carers of adults with learning disability and behaviour that challenges in the UK: Participatory health research.

43. Bringing together coproduction and community participatory research approaches: Using first person reflective narrative to explore coproduction and community involvement in mental health research.

44. A checklist for managed access programmes for reimbursement co‐designed by Canadian patients and caregivers.

45. Online community engagement in response to COVID‐19 pandemic.

46. Cultural animation in health research: An innovative methodology for patient and public involvement and engagement.

47. Preparing researchers for patient and public involvement in scientific research: Development of a hands‐on learning approach through action research.

48. Involving self-help groups in health-care institutions: the patients' contribution to and their view of 'self-help friendliness' as an approach to implement quality criteria of sustainable co-operation.

49. Patient participation in fundamental psychiatric genomics research: a Dutch case study.

50. Redesigning mental health services: lessons on user involvement from the Mental Health Collaborative.