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Clinical Trial Summary

This is a multi-center, prospective, randomized, open-label, controlled trial with two parallel arms and blinded endpoint assessment. It aims yo compare the 6-month efficacy of a group CBT program versus body-mediated intervention (meditation) children (7-13 years) with ADHD-associated FASD and emotional dysregulation via a measurement of the Aggressive Behaviors subscale score of the Dysregulation Profile subset of the CBCL scale.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05273918
Study type Interventional
Source Centre Hospitalier Universitaire de la Réunion
Contact
Status Withdrawn
Phase N/A
Start date January 2023
Completion date October 2028

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