Co-researching consumer experiences of child and adolescent mental health services: Reflections and implications

Families, Systems and Health

Volumn 20, Issue 1, 2002, Pages 75-89

  Byas, Anna ^a   Hills, Deby ^a   Meech, Carole ^a   Read, Lorraine ^a   Stacey, Kathleen ^a   Thompson, Elaine ^a   Wood, Andrew ^a  

^a FLINDERS MEDICAL CENTRE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUSTRALIA; CHILD PSYCHIATRY; CONSUMER; COOPERATION; HEALTH CARE PLANNING; HUMAN; MEDICAL DECISION MAKING; MEDICAL LITERATURE; MEDICAL RESEARCH; MENTAL HEALTH SERVICE; OUTCOMES RESEARCH; PATIENT SATISFACTION; PRACTICE GUIDELINE; REIMBURSEMENT;

EID: 0036186245     PISSN: 10917527     EISSN: None     Source Type: Journal    
DOI: 10.1037/h0089484     Document Type: Article

References (56)

1. Standards, multiple relationships, and the job of therapy and discipline
2. The therapeutic relationship
3. Driving the research agenda
4. Involving service users in mental health services: Social Services Departments and the National Health Service and Community Care Act 1990
5. Consumer and community participation in health research
6. Breathing life into collaborative research: Designing research from the ground up
7. Beyond "bad manners": The power relations of "consumer participation" in Ontario's community mental health system
8. Collaboration for mental health
9. Lay perspectives: Advantages for health research
10. Frogs without legs are deaf: How traditional research can often lead to faulty conclusions
11. Family therapy research: Science into practice, practice into science
12. Social work and empowerment-based research: Possibilities, process and questions
13. Involving patients in clinical research improves the quality of research
14. The rights of patients in research
15. Collaboration: A social work practice method
16. Working with women of color: An empowerment perspective
17. Research collaboration: A politico-ethical approach to effective partnerships
18. Consumer health research
19. Consumer participation in research and health care
20. The importance of considering clients' perspectives in psychotherapy research
21. Participatory research maximises community and lay involvement
22. How can health service users contribute to the NHS research and development programme?
23. Users of health services: Following their agenda
24. Collaboration for mental health: A consumer perspective
25. Qualitative data and the subjectivity of 'objective' facts
26. Understanding alliances. How can research inform user-friendly practice?
27. A consumer-constructed scale to measure empowerment among users of mental health services
28. Consumer empowerment in mental health organizations: Concept, benefits and impediments
29. The rat speaks back: A consumer perspective of the research process
30. Duality: Salient issue or red herring?
31. The relationship between change and satisfaction: Parents' experiences in a child and adolescent mental health service
32. More than protest: Further explorations of alternative metaphors in narrative work
33. From patients' rights to consumers' rights: Historical reflections on the evolution of a concept
34. The ethics of dual relationships
35. Commentary on "Duality: Salient issue or red herring?"
36. What is consumer research?