Table 2 Health-related quality of life as assessed by caregivers (n = 16) and self-reported by the participants (n = 12), according to the Cerebral Palsy Quality of Life questionnaire (CP QOL).
Domain | Baseline | Post-training | P-value | |
|---|---|---|---|---|
Caregivers | Access to services | 63 ± 5 | 67 ± 5 | 0.14 |
Communication & physical health | 69 ± 2 | 68 ± 2 | 0.40 | |
Family health | 59 ± 2 | 60 ± 2 | 0.67 | |
Feelings about functioning | 60 ± 4 | 60 ± 4 | 0.99 | |
General well-being and participation | 66 ± 2 | 71 ± 2 | 0.002 | |
Pain and impact of disability | 60 ± 6 | 76 ± 6 | <0.0001 | |
School well-being | 65 ± 3 | 70 ± 3 | 0.014 | |
Social well-being | 83 ± 3 | 84 ± 3 | 0.58 | |
Global quality of life | 66 ± 2 | 70 ± 2 | 0.037 | |
Participant | Communication & physical health | 78 ± 7 | 78 ± 7 | 0.87 |
Feelings about functioning | 55 ± 5 | 63 ± 5 | 0.06 | |
General well-being and participation | 76 ± 8 | 77 ± 8 | 0.67 | |
Pain and impact of disability | 94 ± 14 | 87 ± 14 | 0.10 | |
School well-being | 77 ± 9 | 78 ± 9 | 0.65 | |
Social well-being | 90 ± 4 | 85 ± 4 | 0.16 | |
Global quality of life | 78 ± 7 | 78 ± 7 | 0.88 |