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| ID | Type | Description | Link |
|---|---|---|---|
| K23MH071320 | U.S. NIH Grant/Contract | View source | |
| DSIR 8K-RTCT |
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| Name | Class |
|---|---|
| National Institute of Mental Health (NIMH) | NIH |
| Rutgers University | OTHER |
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | Interpersonal Psychotherapy-Adolescent Skills Training (IPT-AST) |
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| 2 | Experimental | Enhanced IPT-AST |
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| 3 | Active Comparator | Typical school counseling |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| IPT-AST | Behavioral | IPT-AST is a school based group treatment program that focuses on prevention, psychoeducation, and interpersonal skill building. |
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| Measure | Description | Time Frame |
|---|---|---|
| Score on the Center for Epidemiologic Studies Depression Scale | Measured immediately post-treatment and at Months 6, 12, and 18 follow-ups | |
| Rating on Children's Global Assessment Scale | Measured 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 instrument | Measured immediately post-treatment and at Months 6, 12, and 18 follow-ups |
| Measure | Description | Time Frame |
|---|---|---|
| Score on the Conflict Behavior Questionnaire | Measured immediately post-treatment and at Months 6, 12, and 18 follow-ups | |
| Score on the Social Adjustment Scale | Measured immediately post-treatment and at Months 6, 12, and 18 follow-ups |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jami F. Young, PhD | Rutgers University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Rutgers University | Piscataway | New Jersey | 08554 | United States | ||
| New York State Psychiatric Institute |
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| ID | Term |
|---|---|
| D003863 | Depression |
| ID | Term |
|---|---|
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
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| Enhanced IPT-AST | Other | Enhanced IPT-AST entails IPT-AST plus three parent-adolescent sessions. |
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| School counseling | Other | Usual care consists of standard treatments, including individual counseling with guidance counselor. |
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| Score on the Perceived Social Support scale | Measured immediately post-treatment and at Months 6, 12, and 18 follow-ups |
| New York |
| New York |
| 10032 |
| United States |