A life needs model of pediatric service delivery: Services to support community participation and quality of life for children and youth with disabilities

Physical and Occupational Therapy in Pediatrics

Volumn 22, Issue 2, 2002, Pages 53-77

  King, Gillian ^a   Tucker, Mary Ann ^a   Baldwin, Patricia ^a   Lowry, Karen ^a   LaPorta, John ^a   Martens, Louisa ^a  

^a THAMES VALLEY CHILDREN S CENTRE   (Canada)

Author keywords

Childhood disability; Model; Participation; Quality of life; Rehabilitation; Service delivery

Indexed keywords

ADOLESCENT; ADULT; CHILD; CHILD DEVELOPMENT; CHILD HEALTH CARE; COMMUNITY CARE; DISABILITY; FAMILY; HEALTH CARE DELIVERY; HEALTH CARE PLANNING; HUMAN; LIFE EVENT; MOTIVATION; PRACTICE GUIDELINE; QUALITY OF LIFE; REVIEW; SOCIAL CARE; STRENGTH;

ADOLESCENT; CANADA; CHILD; CHILD HEALTH SERVICES; COMMUNITY HEALTH SERVICES; DEVELOPMENTAL DISABILITIES; DISABLED CHILDREN; FEMALE; HUMANS; MALE; MODELS, ORGANIZATIONAL; NEEDS ASSESSMENT; OCCUPATIONAL THERAPY; PATIENT CARE TEAM; PEDIATRICS; PHYSICAL THERAPY MODALITIES; QUALITY OF LIFE; RESEARCH DESIGN; SOCIAL SUPPORT;

EID: 0036356926     PISSN: 01942638     EISSN: None     Source Type: Journal    
DOI: 10.1300/J006v22n02_04     Document Type: Review

References (73)

1. Rethinking family-centered practice
2. Assessing needs of families with handicapped infants
3. Quality of life for mentally retarded people in Germany: An overview of theory and practice
4. Models of disablement, universalism and the international classification of impairments, disabilities, and handicaps
5. Models of helping and coping
6. Opportunities for health promotion: Including the chronically ill and disabled
7. Children at risk: Fostering resilience and hope
8. Community action for health promotion: A strategy to empower individuals and communities
9. A quality of life model: New challenges arising from a six year study
10. Working with parents of exceptional children: The need for more careful thought and positive action
11. Lay concepts of health
12. Developments in family systems theory and research
13. Transition of young children into the elementary education mainstream
14. Quality of life as context for planning and evaluation of services for people with disabilities
15. Coping with disabilities: The perspective of young adults from different ethnic backgrounds in inner London
16. Enabling and empowering families of children with health impairments
17. Exploring current conceptions of quality of life: A model for people with and without disabilities
18. The national quality of life for persons with disabilities project: A quality of life agenda for the United States
19. Disability and the transition to adulthood: Issues for the disabled child, the family, and the pediatrician
20. Transition: A look at the foundations
21. The transition from early intervention to kindergarten: Parental satisfaction and involvement
22. Who does well - Why?
23. Parent involvement
24. Success in life for older adolescents with cerebral palsy
25. Interpersonal aspects of care-giving and client outcomes: A review of the literature
26. Parents' and service providers' perceptions of the family-centeredness of children's rehabilitation services
27. Social skills training for withdrawn unpopular children with physical disabilities: A preliminary evaluation
28. Parents' perceptions of caregiving: Development and validation of a measure of processes
29. Social outcome of handicapped children as adults
30. Family-centred functional therapy for children with cerebral palsy: An emerging practice model
31. Perspectives on understanding and changing the environments of children with disabilities
32. Infant and toddler models of service delivery: Are they detrimental for some children and families?
33. The family-centered consultation model: Practical applications for professionals
34. Youth, disability and quality of life
35. Predicting elementary school participation in children with disabilities
36. Quality of life as the criterion for need assessment and community psychology
37. Peer-mediated approaches to promoting children's social interaction: A review
38. Early intervention in children with Down's syndrome: From evaluation to methodology
39. Assessing the quality of life of persons with developmental disabilities: Description of a new model, measuring instruments, and initial findings
40. Studying the lives of persons with developmental disabilities: Methodological lessons from the quality of life project
41. The Centre for Health Promotion's conceptual approach to quality of life: Being, belonging, and becoming
42. Quality of life: Linking a conceptual approach to service provision
43. Quality of life and rehabilitation
44. Overcoming the social construction of inequality as a prerequisite to quality of life
45. Family-centred service: A conceptual framework and research review
46. Transactional regulation and early intervention
47. Quality of life: Its measurement and use
48. The idea of health: Doing foundational inquiry
49. Developing resiliency in children from disadvantaged populations
50. Community-based care: Back to the future!
51. Perceptions of health among adults with disabilities
52. In support of research on quality of life, but against QOL
53. Physically disabled people assess the quality of their lives
54. Patients in transition: Bridging the health care gap from youth to adulthood
55. Quality of life as a rehabilitation outcome: Are we missing the boat?
56. Being, belonging, becoming: An approach to the quality of life of persons with developmental disabilities
57. Constitution of the World Health Organization