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. 2021 Nov 1;12:733978. doi: 10.3389/fneur.2021.733978

Table 3.

Distribution and variation of QoL of individuals with CP from childhood to young adulthood: SPARCLE cohort—France, Germany, Italy, and Sweden.

All participants (n = 164) Participants in all waves (n = 130)
Psychological well-being Social relationships Psychological well-being Social relationships
Childhood
n 142 140 123 119
Mean (SD) 73.9 (18.1) 50.2 (26.7) 74.2 (18.6) 51.3 (26.2)
[Min–max] [20.0–100.0] [0.0–100.0] [20.0–100.0] [0.0–100.0]
Adolescence
n 144 143 123 119
Mean (SD) 71.1 (20.7) 53.5 (27.5) 73.5 (19.2) 56.7 (26.7)
[Min–max] [0.0–100.0] [0.0–100.0] [16.7–100.0] [0.0–100.0]
Young adulthood
n 155 160 123 119
Mean (SD) 61.7 (13.2) 66.7 (20.8) 63.1 (12.5) 68.3 (19.5)
[Min–max] [25.0–87.5] [0.0–100.0] [25.0–87.5] [8.3–100.0]
Change in QoL scores*
β −0.78 1.24 −0.81 1.12
[95% CI] [−0.99 to −0.56] [0.92 to 1.55] [−1.04 to −0.58] [0.79 to 1.46]

QoL, quality of life; CP, cerebral palsy.

*

β coefficients and 95% CI estimated by generalized linear mixed-effect model with random intercept adjusted for region, sex, and parental education level. β coefficients show the average difference in quality of life by 1 year of age.

95% CI excluding zero.