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. Author manuscript; available in PMC: 2019 Aug 1.
Published in final edited form as: Psychooncology. 2018 Jun 29;27(8):2031–2038. doi: 10.1002/pon.4769

Table 1:

Characteristics of children and parents and outcomes of interest (N=213)

Demographics Mean (SD)/Range Median (IQR)
Child age at diagnosis (years) 6.6 (4.5)/1-18 5.0 (5.5)
Child age at evaluation (years) 14.3 (4.8)/8-23 13.2 (7.1)
Maternal education (years) 13.7 (2.6)/4-20 13.0 (4.0)
Child’s sex N (percentage)
  Male 109 (51.2%)
  Female 104 (48.8%)
Parent’s sex
  Male 40 (18.8%)
  Female 173 (81.2%)
Child’s race/ethnicity N (percentage)
  White, non-Hispanic 157 (73.7%)
  Black, non-Hispanic 27 (12.7%)
  Hispanic 17 (8.0%)
  Other 12 (5.6%)
Treatment Factors Mean (SD) Median (IQR)
Time since diagnosis (years) 7.7 (1.7) 7.5 (2.7)
Treatment intensity N (percentage)
  Standard/High risk 91 (42.7%)
  Low risk 122 (57.3%)
Survey Outcomes Mean (SD) Median (IQR)
Family cohesiona 2.4 (1.5) 2.0 (2.0)
Parental distressa, b 42.6 (9.6) 39.0 (11.0)
Parental protective behaviora, b 23.9 (7.9) 24.0 (9.5)
Child overall symptom burden c 84.5 (14.8) 83.5 (21.0)
Child HRQOLc 80.6 (15.9) 84.5 (21.0)
Family straina 44.6 (13.8) 43.0 (22.0)

IQR: Interquartile range

a

Higher scores indicate worse outcomes

b

Based on clinically meaningful cut-points, 16% of parents of childhood cancer survivors had global distress, and 22% of parents engaged in overprotective behaviors

c

Higher scores indicate better outcomes (Table 1 only); also see notes for the scoring direction in Tables 23 and Supplement Tables)