Group-Based Symptom Trajectories in Indicated Prevention of Adolescent Depression
Article [Author's Original]
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Depression and anxiety ; vol. 33, no. 5, pp. 444-451.Abstract(s)
Background: Adolescent 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 preven-
tion trials and examine how cognitive-behavioral (CB) interventions and baseline
predictors relate to trajectory membership.
Methods: Six 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.
Results: We
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 dis-
tinguished by baseline symptom severity. Two trajectories of negative course
(high-persistent, resurging), respectively, showed no decline in symptoms or de-
cline 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 rel-
ative to other trajectories.
Conclusions: Findings 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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