Item Development and Preliminary Validation of the Variability in Adverse Childhood Experiences Scale (VACE)
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Published on: April 23, 2014
Mary Jo Hedrick1, Jessica Templeton2, Andrei Sigunov2
1Center of Excellence in Early Childhood Learning and Development, East Tennessee State University, Johnson City, USA.
Abstract:
This study presents initial item development and psychometric evaluation of the Variability in Adverse Childhood Experiences Scale (VACE), a frequency-based modification of the Adverse Childhood Experiences Scale (The ACE Scale; Felitti et al., 1998) designed to address limitations of binary scoring by capturing the frequency of adversity exposure within established ACE domains. Undergraduate and community participants (N = 370) completed the VACE, the Childhood Trauma Questionnaire-Short Form (CTQ-SF), and measures of depressive symptoms, perceived stress, and substance use. Psychometric evaluation included internal consistency, test-retest reliability across a two-week interval, exploratory factor analysis, convergent validity, and incremental predictive validity using hierarchical regression analyses. Internal consistency was acceptable (α = 0.79) and test-retest reliability was good (ICC = 0.66, 95% CI [0.40, 0.84], p < .001). Exploratory factor analysis supported a two-factor structure reflecting Direct and Interpersonal Adversity and Community and Contextual Adversity (r = .56), consistent with the multidimensional nature of childhood adversity. The VACE was significantly correlated with the CTQ-SF (r = .76, p < .001), supporting convergent validity. Hierarchical regression analyses indicated that VACE frequency scores explained significant incremental variance in depressive symptoms (ΔR² = 0.042, p < .001), perceived stress (ΔR² = 0.056, p < .001), and substance use (ΔR² = 0.021, p = .004) beyond traditional binary ACE scoring. These findings provide preliminary psychometric support for frequency-based adversity measurement as a complement to existing ACE frameworks. The VACE retains compatibility with established ACE scoring while offering dimensional precision that may better capture dose-response relationships between adversity and health outcomes. Replication in more diverse samples and longitudinal validation are warranted.
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