Skip to main content
Clinical Trials/NCT02054312
NCT02054312
Completed
Not Applicable

Phase II Study of Family Based Interpersonal Psychotherapy (FB-IPT) for Depressed Preadolescents

University of Pittsburgh1 site in 1 country42 target enrollmentOctober 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depressive Disorders
Sponsor
University of Pittsburgh
Enrollment
42
Locations
1
Primary Endpoint
Childhood Depression Rating Scale -Revised
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The investigators proposed a preliminary randomized control trial of Family Based Interpersonal Psychotherapy (FB-IPT), a family-based adaptation of Interpersonal Psychotherapy for Depressed Adolescents (IPT-A; Mufson et al., 2000). Forty-five preadolescent children (ages 8-12) diagnosed with a depressive disorder will be randomized to receive a 14-week course of FB-IPT or Client Centered Therapy (CCT), a supportive nondirective psychotherapy that closely approximates treatment at usual in community mental health clinics. In addition to assessing the feasibility and acceptability of randomization and each of the treatment conditions, this project will evaluate the effects of FB-IPT and CCT across multiple domains, including symptomatology and psychosocial functioning. Preadolescents will be assessed prior to treatment, during treatment (Weeks 3, 7, 11), one week post-treatment, and at 3 and 6 months post-treatment to compare changes in depressive symptoms, global, social, and family functioning. Data on psychosocial risk factors associated with onset and recurrence of preadolescent depression will be collected prior to treatment and at specified intervals post-treatment in order to conduct exploratory analyses on correlates of positive and negative treatment outcomes for Family Based IPT. This data will be used to generate future hypotheses about potential mediators and moderators that will be incorporated into an R01 application for an efficacy study of Family Based IPT.

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
October 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Laura Dietz

Assistant Professor

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • current depressive disorder
  • one parent must be willing to participate in treatment

Exclusion Criteria

  • bipolar disorder
  • recent abuse
  • developmental delay
  • autism spectrum disorder

Outcomes

Primary Outcomes

Childhood Depression Rating Scale -Revised

Time Frame: 15 weeks

Study Sites (1)

Loading locations...

Similar Trials