Interrater reliability of the Anxiety Disorders Interview Schedule for DSM-IV: child and parent version.
Heidi J Lyneham, Maree J Abbott, Ronald M Rapee
https://pubmed.ncbi.nlm.nih.gov/17513985/Actively Recruiting
Led by Ggz Oost Brabant · Updated on 2026-05-07
236
Participants Needed
1
Research Sites
N/A
Total Duration
Depression is a significant health concern among adolescents, with a notable number experiencing major depressive disorder or depressive symptoms. This research focuses on Dutch adolescents attending special schools, a group at higher risk for developing depression and suicidal thoughts. The study aims to screen these adolescents, offer a prevention program, and assess its impact on depressive symptoms, suicidality, anxiety, and somatic complaints through a randomized controlled trial. The study compares two groups one receiving the CBT-based preventive group training called Op Volle Kracht, adapted for special education settings, which includes eight weekly 45-minute sessions plus a follow-up meeting and a control group that is monitored and offered the training later if it proves effective. All participating schools teachers receive training to recognize and address depressive and suicidal symptoms. Clinical interviews and questionnaires are used at several points to measure outcomes. Participants will complete assessments at baseline, post-intervention, and at 6 and 12 months follow-up, including clinical interviews and self-report questionnaires about depressive symptoms and related concerns. Those showing suicidality will be referred to specialized care with parental involvement. The study includes ongoing guidance and mental health support as needed, aiming to evaluate the prevention programs effectiveness to better support adolescents in special education over a total period of up to 12 months post-intervention.
CONDITIONS
Depression and Suicide Prevention in Adolescents Attending Special Schools
W
Wendy CH Rongen, MSc
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Ggz Oost Brabant
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - 9 weeks
Participants in the intervention group attend the Op Volle Kracht preventive group training based on cognitive behavioural therapy for depression. This program consists of eight weekly 45-minute meetings and one short weekly follow-up meeting for repetition, held at school during school hours.
Weekly visits for 9 weeks
Duration - 12 months
Participants complete clinical interviews and self-report questionnaires to assess depressive symptoms and suicidality at several time points after the intervention.
Assessments at baseline, post-intervention (12 weeks), 6 months, and 12 months
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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Heidi J Lyneham, Maree J Abbott, Ronald M Rapee
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https://pubmed.ncbi.nlm.nih.gov/17905048/Ggz Oost Brabant
Lead Sponsor