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Comparison of Three Therapy-Based Interventions for Preventing Depression in Adolescents

Prevention of Depression in Adolescents

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00258752
Enrollment
57
Registered
2005-11-28
Start date
2005-11-30
Completion date
2009-06-30
Last updated
2020-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Keywords

Prevention, Adolescent

Brief summary

This study will compare Interpersonal Psychotherapy-Adolescent Skills Training (IPT-AST), IPT-AST plus parent involvement (Enhanced IPT-AST), and Usual Care for the prevention of adolescent depression.

Detailed description

Depression is a serious medical illness that is difficult to diagnose and treat, especially in children and adolescents. Signs of depression in children may include the following behaviors: pretending to be sick; refusing to go to school; clinging to a parent; or worrying that a parent may die. Older children may sulk, behave inappropriately at school, act in a negative or grouchy manner, or feel misunderstood. Because normal behaviors vary from one childhood stage to another, it can be difficult to determine whether a child is going through a temporary phase or is suffering from depression. This study will compare IPT-AST, Enhanced IPT-AST, and Usual Care for the prevention of adolescent depression. Participation in this single-blind study will last approximately 21 months. Participants will be randomly assigned to receive either IPT-AST, Enhanced IPT-AST, or Usual Care for 12 weeks. IPT-AST is a school-based group intervention program that focuses on prevention, psychoeducation, and interpersonal skill-building. Enhanced IPT-AST will entail IPT-AST plus three parent-adolescent sessions. Usual Care will consist of standard treatments and will not include IPT-AST. Study visits will occur before and during the intervention at baseline and Weeks 6 and 12. Follow-up visits will occur 6, 12, and 18 months post-intervention. Study visit assessments will include depression symptoms, anxiety symptoms, psychiatric diagnoses, overall functioning, social adjustment, parent-child conflict, perceived support from parents and peers, and service utilization.

Interventions

BEHAVIORALIPT-AST

IPT-AST is a school based group treatment program that focuses on prevention, psychoeducation, and interpersonal skill building.

OTHEREnhanced IPT-AST

Enhanced IPT-AST entails IPT-AST plus three parent-adolescent sessions.

OTHERSchool counseling

Usual care consists of standard treatments, including individual counseling with guidance counselor.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Rutgers University
CollaboratorOTHER
Children's Hospital of Philadelphia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
11 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Between grades 7 and 10 in school * Score of at least 16 on the Center for Epidemiologic Studies Short Depression Scale (CES-D) * Currently experiencing at least 2 symptoms on the K-SADS depression section, one of which is either depressed mood, irritability, or an inability to feel pleasure during normal activities * Score of at least 61 on the Children's Global Assessment Scale (CGAS), indicating mild to moderate impairment * English-speaking

Exclusion criteria

* Score of 15 or less on the CES-D scale * Currently experiencing fewer than 2 depression symptoms on the K-SADS or 2 or more symptoms on the K-SADS with no report of depressed mood, irritability, or anhedonia * Attempted suicide or self-mutilation in the year prior to study entry * Current active suicidal ideation and/or history of a clinically significant suicidal behavior (i.e., with intent to die and high medical lethality) or repeated patterns of self-injurious behavior * Current major depressive disorder or dysthymia as determined by K-SADS * Current DSM-IV diagnosis of psychosis, substance abuse or dependence, bipolar disorder, obsessive compulsive disorder, post-traumatic stress disorder, panic disorder, or conduct disorder as determined by K-SADS * Score of 60 or less on the CGAS, indicating substantial functional impairment

Design outcomes

Primary

MeasureTime frame
Score on the Center for Epidemiologic Studies Depression ScaleMeasured immediately post-treatment and at Months 6, 12, and 18 follow-ups
Rating on Children's Global Assessment ScaleMeasured immediately post-treatment and at Months 6, 12, and 18 follow-ups
Depression diagnoses on the Kiddie Schedule for Affective Disorders and Schizophrenia (K-SADS) diagnostic instrumentMeasured immediately post-treatment and at Months 6, 12, and 18 follow-ups

Secondary

MeasureTime frame
Score on the Conflict Behavior QuestionnaireMeasured immediately post-treatment and at Months 6, 12, and 18 follow-ups
Score on the Social Adjustment ScaleMeasured immediately post-treatment and at Months 6, 12, and 18 follow-ups
Score on the Perceived Social Support scaleMeasured immediately post-treatment and at Months 6, 12, and 18 follow-ups

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026