International development and psychometric properties of the Child and Adolescent Trauma Screen (CATS).
Cedric Sachser, Lucy Berliner, Tonje Holt...
https://pubmed.ncbi.nlm.nih.gov/28049104/Actively Recruiting
Led by University Children's Hospital, Zurich · Updated on 2026-01-26
1200
Participants Needed
11
Research Sites
N/A
Total Duration
Researchers are studying the PTSD-iMPACT questionnaire, a new tool designed to measure how post-traumatic stress symptoms affect daily functioning in children and adolescents aged 3 to 18 years. The study aims to validate this tool in both clinical and non-clinical populations in Switzerland and Germany. It addresses a need for a reliable, detailed measure of PTSD-related impairments across areas like family, school, friendships, hobbies, and media use. The study involves collecting data from trauma-exposed children, adolescents, and their caregivers through self-report and caregiver-report versions of the PTSD-iMPACT. Participants complete questionnaires at baseline and again two weeks later for test-retest reliability. Data collection occurs in clinical settings and schools, with some assessments completed online or via phonevideo calls. The study is conducted over 13 months and includes both German-speaking clinical populations and a non-clinical sample in Switzerland. Participants provide information on trauma exposure, PTSD symptoms, depression, anxiety, quality of life, and emotional regulation, among other measures. The study uses statistical analyses to assess the reliability and validity of the PTSD-iMPACT tool. Participants in clinical groups complete two assessments, while non-clinical participants complete one. Study involvement includes completing questionnaires online or in person with support provided as needed, ensuring confidentiality and voluntary participation throughout the study.
CONDITIONS
Development of the PTSD-iMPACT to Measure PTSD-Related Functional Impairment in Children and Adolescents - A Validation Study in Switzerland and Germany
L
Lasse Bartels, Dr.
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University Children's Hospital, Zurich
Lead Sponsor
University Clinic for Child and Adolescent Psychiatry, Psychosomatics, and Psychotherapy, Carl von Ossietzky University of Oldenburg, Oldenburg, Germany
Collaborating Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or virtual) for eligibility confirmation and consent
Duration - Single assessment session
Participants complete the initial PTSD-iMPACT questionnaire and other related assessments to evaluate PTSD-related functional impairment and associated psychological measures.
1 visit (in-person, virtual call, or online survey) for questionnaire completion; approximately 40 minutes
Duration - 2 weeks after baseline
Participants complete a follow-up questionnaire battery two weeks after the baseline to assess test-retest reliability of PTSD-iMPACT and related measures.
1 visit (virtual call or online survey) approximately 15 minutes; only for clinical populations
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Lead Sponsor
University Clinic for Child and Adolescent Psychiatry, Psychosomatics, and Psychotherapy, Carl von Ossietzky University of Oldenburg, Oldenburg, Germany
Collaborating Sponsor