Methods: The design of the study was a controlled trial. In total, at T1 screening data of 3636 children were collected, of which 333 participated in the program. The no-intervention control group consisted of 157 children. Pre- and post-intervention (T1 and T2) data on severity of anxiety and depression symptoms as reported by the child, the teacher, and all classmates (peer report) were analyzed. In the intervention group also data on program integrity using classroom based observations and prevention professionals’ reports tapping adherence to protocol, quality of delivery, participant responsiveness, and exposure were collected.
Results: Preliminary analyses using multilevel linear regression adjusting for baseline (T1) scores, age, gender and ethnicity, showed that children in the intervention group experienced significantly fewer symptoms of anxiety and depression on 5 scales of the Revised Child Anxiety and Depression Scale (RCADS) at T2. Differences were for the total internalizing scale: -6.15 95%CI[-10.38,-1.92]; total anxiety scale: -4.40 95%CI[-7.89,-0.92]; social phobia: -1.70 95%CI[-2.73,-0.67]; obsessive compulsive disorder: -0.79 95%CI[-1.48,-0.10]; and major depressive disorder: -1.67 95%CI[-2.67,-0.66].
Conclusions: Preliminary results show that FRIENDS for Life significantly reduces symptoms of anxiety and depression. In further analyses we will examine possible moderators, and the relation between participants’ evaluation, program integrity and outcomes. Results will be used to guide implementation and dissemination activities in the Netherlands.