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Evaluating the global psychotrauma screen total score using item response theory in an Italian community sample
Antony Bologna1, Rodolfo Rossi2, Tommaso Barlattani1
1Department of Biotechnological and Applied Clinical Sciences (DISCAB), University of L'Aquila, L'Aquila, Italy.
Abstract:
Background: The Global Psychotrauma Screen (GPS) is a brief transdiagnostic screener for trauma-related symptoms. Although the Italian version has previously been examined using factor-analytic methods, evidence on item-level functioning and on the interpretability of the symptom total remains limited.Objective: To determine whether the 17 GPS symptom items support the use of a single total score as an efficient indicator of global trauma-related burden.Method: Data from an age- and gender-balanced analytic sample of 6930 Italian adults recruited online during the COVID-19 outbreak were analysed. Essential unidimensionality was examined using parallel analysis and bifactor indices (ECVg and ωH). One- and two-parameter logistic IRT models were compared, and item fit, local dependence, test information, conditional reliability, and sensitivity to aberrant responding were evaluated.Results: Bifactor indices supported essential unidimensionality (ECVg = 0.73; ωH = 0.77). The 2PL model outperformed the 1PL model and showed acceptable global fit (RMSEA = 0.058, SRMSR = 0.04, TLI = 0.94, CFI = 0.94). Item discrimination ranged from 0.68 to 3.03, and item difficulty ranged from -0.95 to 2.71. The test information function peaked at θ = -0.24 and indicated useful precision across a broad range of moderate-to-high trauma burden. Item parameters remained stable after removing of respondents with aberrant response patterns.Conclusions: In this community sample, the Italian GPS symptom total can be interpreted as a psychometrically defensible indicator of global trauma-related burden. The scale was especially informative from slightly below-average to elevated levels of severity, supporting its use as a brief first-line screening measure while still requiring replication in independent and clinical samples.