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. Author manuscript; available in PMC: 2012 Mar 1.
Published in final edited form as: J Pediatr Gastroenterol Nutr. 2011 Mar;52(3):295–299. doi: 10.1097/MPG.0b013e3181f5714e

Table 1.

Participant Characteristics

N 62
Adolescent age (years) 15.4 ± 1.4
Gender (% female) 43.5%
Ethnicity (% White, not Hispanic origin) 88.7%
Caregiver status
 Biological Mother (%) 85.5%
 Biological Father (%) 9.7%
 Adoptive Mother (%) 3.2%
 Other (%) 1.6%
Caregiver marital status (% married) 88.7%
Caregiver education level (% with at least a
college degree)
50.0%
Caregiver employment status
(% employed)
86.3%
IBD Diagnosis (%) 6.6 ± 4.0
 Crohn’s Disease 79.0%
 Ulcerative Colitis 21.0%
Disease Severity 9.83 ± 9.75
 PCDAI 11.68 ± 10.0
 LCAI 2.85 ± 3.9
PIP Difficulty 77.8 ± 24.7
CDI (adolescent) 5.85 ± 6.4
IMPACT-III Total Score 144.55 ± 19.9
IMPACT-III General Well-Being 58.03 ± 8.7
IMPACT-III Emotional Functioning 46.15 ± 7.1
IMPACT-III Social Functioning 21.87 ± 2.8
IMPACT-III Body Image 11.32 ± 2.4

Note. Scores are shown as means ± SD. PIP- Pediatric Inventory for Parents; CDI- Childhood Depression Inventory; PCDAI-Pediatric Crohn’s Disease Activity Index; LCAI-Lichtiger Colitis Activity Index.