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Clinical Trial Summary

The primary objective of the BLAME-LESS study is to examine the effectiveness of an online psychoeducation program in reducing trauma-related feelings of shame and guilt in adolescents who experienced sexual or physical abuse .


Clinical Trial Description

The study follows a two-arm RCT (n=34). The effects of a brief online psychoeducation program will be compared, with a waiting-list control group. The intervention aims to reduce feelings of trauma-related shame and guilt that adolescents experience regarding their own defense responses during and after (sexual) violence. Assessments take place after screening, at baseline, two weeks after allocation to the intervention or waiting-list, and, only for the waiting-list participants, seven weeks after allocation to the intervention. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05987735
Study type Interventional
Source Karakter Kinder- en Jeugdpsychiatrie
Contact Rik Knipschild, drs
Phone +31629607864
Email r.knipschild@karakter.com
Status Not yet recruiting
Phase N/A
Start date August 1, 2023
Completion date December 31, 2024

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