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NZCCS Cohort<br />
Nonrespondents<br />
Respondents<br />
(n=396) (n=226) (n=170)<br />
Age range 0 - 16 0 - 15<br />
Time since diagnosis<br />
Median 9.4 9.0 10.0 0.02<br />
Surgery<br />
No 188 47 100 44 88 52 0.14<br />
Yes 208 53 126 54 82 48<br />
Chemotherapy<br />
No 45 11 24 11 21 12 0.59<br />
Yes 351 89 202 89 149 88<br />
Radiation<br />
HSCT<br />
No 295 74 165 73 130 76 0.43<br />
Yes 101 26 61 27 40 24<br />
No 357 90 206 91 151 89 0.44<br />
Yes 39 10 20 9 19 11<br />
p values test for differences between respondents and non-respondents. Chi-square was used for categorical<br />
variables and Mann Whitney U for continuous variables (non normally distributed).<br />
4.2 Research Question 1. Describe the Psychosocial Wellbeing of Childhood<br />
Cancer Survivors<br />
4.2.1 Wellbeing of Childhood Cancer Survivors (WHO-5)<br />
One hundred and sixty nine childhood cancer survivors (CCS) answered the five<br />
items that comprise the WHO-5 wellbeing scale (Cronbach’s α = 0.87). The WHO-5<br />
score ranged from a minimum of 2 to a maximum of 25 (possible range 0 to 25). As<br />
figure 2 shows, the distribution was not normally distributed, with a negative skew<br />
(Skew = -1.0, Kurtosis = 1.17, Kolmogorov-Smirnov = 0.10, p = .05). The mean score<br />
was 18.25 and the median was 19. The majority (89%) of respondents reported good to<br />
excellent wellbeing. Eighteen respondents (11%) scored below the threshold of 13,<br />
indicating poor wellbeing.<br />
P<br />
40