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RECRUITINGOBSERVATIONAL

Development of the PTSD-iMPACT to Measure PTSD-Related Functional Impairment in Children and Adolescents - A Validation Study in Switzerland and Germany

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Population-based and clinical studies indicate that a substantial proportion of children and adolescents are exposed to one or more potentially traumatic events (PTEs) Approximately 16 % of those affected by childhood trauma go on to develop post-traumatic stress disorder (PTSD), with an even higher proportion experiencing subclinical levels of post-traumatic stress symptoms (PTSS). In Switzerland, over half of adolescents report exposure to at least one PTE, with 4.2 % meeting diagnostic criteria for PTSD. PTSD frequently impacts young people's social and educational functioning, often impairing their ability to engage in everyday life activities that are important or meaningful to them. Although the psychological consequences of PTSD are well documented, there is limited empirical understanding of how PTSS specifically affects day-to-day functioning in young people. A key reason for this gap is the absence of a validated instrument specifically designed to assess PTSD-related functional impairment in children and adolescents. To address this need, the PTSD-iMPairment in Adolescent \& Children's Capacity for Thriving (PTSD-iMPACT) measure was developed. This tool aims to systematically assess the extent of PTSD-related functional impairment in children and adolescents across key life domains, such as family, friends, school, apprenticeship, hobbies or media use. The overall aim of this study is to evaluate the psychometric properties of the PTSD-iMPACT questionnaire in a clinical and in a non-clinical sample and to provide an internationally applicable standard instrument for the assessment of PTSD-related functional impairment in trauma-exposed children and adolescents. In the long term, the aim is to ensure that the care and support provided to children and adolescents who experience difficulties in their daily lives due to post-traumatic stress symptoms are sustainably monitored and improved.

Who May Be Eligible (Plain English)

Clinical population Who May Qualify: - Use of (mental) health services at a participating study center. - Children and adolescents between 7 and 18 years / caregivers of children and adolescents between 3 and 18 years - Sufficient knowledge of the German language - Signed consent form (7-18 years: patient and caregiver; 3-6 years: caregivers) Who Should NOT Join This Trial: - Children and adolescents under 7 or over 18 years / caregivers of children and adolescents under 3 or over 18 years - Not sufficient knowledge of the German language - No signed consent form (7-18 years: patient and/or caregiver; 3-6 years: caregivers) Non-clinical population Only recruited in Switzerland. Who May Qualify: - Students between 3rd grade and 18 years / caregivers of kindergarteners and students up until 18 years - Sufficient knowledge of the German language Who Should NOT Join This Trial: - Students 2nd grade or lower and over 18 years / caregivers of children not yet in Kindergarten and students over 18 years - No sufficient knowledge of the German language Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Clinical population Inclusion Criteria: * Use of (mental) health services at a participating study center. * Children and adolescents between 7 and 18 years / caregivers of children and adolescents between 3 and 18 years * Sufficient knowledge of the German language * Signed consent form (7-18 years: patient and caregiver; 3-6 years: caregivers) Exclusion Criteria: * Children and adolescents under 7 or over 18 years / caregivers of children and adolescents under 3 or over 18 years * Not sufficient knowledge of the German language * No signed consent form (7-18 years: patient and/or caregiver; 3-6 years: caregivers) Non-clinical population Only recruited in Switzerland. Inclusion Criteria: * Students between 3rd grade and 18 years / caregivers of kindergarteners and students up until 18 years * Sufficient knowledge of the German language Exclusion Criteria: * Students 2nd grade or lower and over 18 years / caregivers of children not yet in Kindergarten and students over 18 years * No sufficient knowledge of the German language

Locations (11)

Traumaambulanz, Universitätsklinikum Aachen
Aachen, Germany
Otto-Friedrich-Universität Bamberg
Bamberg, Germany
Lehrstuhl für Klinische Psychologie und Kinder- und Jugendlichenpsychotherapie, Katholische Universität Eichstätt-Ingolstadt
Eichstätt, Germany
Zentrum für Psychotherapie Bodensee (apb)
Konstanz, Germany
Kinder- und Jugendlichen-Psychotherapie-Ambulanz (KJ-PAM) Marburg
Marburg, Germany
Universitätsklinik für Kinder- und Jugendpsychiatrie, Psychosomatik und Psychotherapie Carl von Ossietzky Universität Oldenburg
Oldenburg, Germany
Child and Adolescent Psychiatry Ulm University
Ulm, Germany
Child and Adolescent Psychiatric Services Thurgau
Frauenfeld, Switzerland
• Parent-Child Consultation 0-5 of The Child and Adolescent Psychiatric Services St. Gallen
Sankt Gallen, Switzerland
Cantonal Hospital Winterthur
Winterthur, Switzerland
University Children's Hospital Zurich
Zurich, Switzerland