BackgroundAdolescent depression prevention research has focused on mean intervention outcomes, but has not considered heterogeneity in symptom course. Here, we empirically identify subgroups with distinct trajectories of depressive symptom change among adolescents enrolled in two indicated depression prevention trials and examine how cognitive-behavioral (CB) interventions and baseline predictors relate to trajectory membership. MethodsSix hundred thirty-one participants were assigned to one of three conditions: CB group intervention, CB bibliotherapy, and brochure control. We used group-based trajectory modeling to identify trajectories of depressive symptoms from pretest to 2-year follow-up. We examined associations between class membership and conditions using chi-square tests and baseline predictors using multinomial regressions. ResultsWe identified four trajectories in the full sample. Qualitatively similar trajectories were found in each condition separately. Two trajectories of positive symptom course (low-declining, high-declining) had declining symptoms and were distinguished by baseline symptom severity. Two trajectories of negative course (high-persistent, resurging), respectively, showed no decline in symptoms or decline followed by symptom reappearance. Participants in the brochure control condition were significantly more likely to populate the high-persistent trajectory relative to either CB condition and were significantly less likely to populate the low-declining trajectory relative to CB group. Several baseline factors predicted trajectory classes, but gender was the most informative prognostic factor, with males having increased odds of membership in a high-persistent trajectory relative to other trajectories. ConclusionsFindings suggest that CB preventive interventions do not alter the nature of trajectories, but reduce the risk that adolescents follow a trajectory of chronically elevated symptoms.
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Univ Newcastle, Inst Neurosci, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
Univ Paris Est, Fac Med, UMR S 955, F-94010 Creteil, France
Fdn Fondamental, F-94010 Creteil, FranceUniv Bordeaux, EA4139, F-33000 Bordeaux, France
Scott, Jan
Henry, Chantal
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INSERM, Unite U955, F-94010 Creteil, France
Univ Paris Est, Fac Med, UMR S 955, F-94010 Creteil, France
AP HP, Grp Henri Mondor Albert Chenevier, F-94010 Creteil, France
Fdn Fondamental, F-94010 Creteil, FranceUniv Bordeaux, EA4139, F-33000 Bordeaux, France
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Carnegie Mellon Univ, H John Heinz III Sch Publ Policy & Management, Pittsburgh, PA 15213 USACarnegie Mellon Univ, H John Heinz III Sch Publ Policy & Management, Pittsburgh, PA 15213 USA
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Tsinghua Univ, Dept Sociol, Xiongzhixing Bldg 206, Beijing 100084, Peoples R ChinaTsinghua Univ, Dept Sociol, Xiongzhixing Bldg 206, Beijing 100084, Peoples R China
Wang, Yuhang
Li, Buqun
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Tsinghua Univ, Dept Sociol, Xiongzhixing Bldg 206, Beijing 100084, Peoples R ChinaTsinghua Univ, Dept Sociol, Xiongzhixing Bldg 206, Beijing 100084, Peoples R China
Li, Buqun
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Zhang, Chenggang
Buxton, Orfeu M.
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Penn State Univ, Dept Biobehav Hlth, State Coll, PA USATsinghua Univ, Dept Sociol, Xiongzhixing Bldg 206, Beijing 100084, Peoples R China
Buxton, Orfeu M.
Redline, Susan
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Brigham & Womens Hosp, Dept Med, Div Sleep & Circadian Disorders, Boston, MA USA
Harvard Med Sch, Boston, MA USATsinghua Univ, Dept Sociol, Xiongzhixing Bldg 206, Beijing 100084, Peoples R China