Parent Psychoeducation and Cognitive Behavior Therapy for Latino Adolescents With Depression

Sponsor
National Institute of Mental Health (NIMH) (NIH)
Overall Status
Unknown status
CT.gov ID
NCT00118469
Collaborator
(none)
144
1
53
2.7

Study Details

Study Description

Brief Summary

This study will determine the effectiveness of adding a parent-involved intervention to cognitive behavior therapy in reducing depressive symptoms among Latino adolescents with depression.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Psychoeducation
  • Behavioral: Cognitive behavior therapy
Phase 2

Detailed Description

Adolescent depression can have a devastating impact on social, emotional, and family functioning. Cognitive behavior therapy (CBT) is the most common treatment for depression; however, not all patients respond adequately to CBT. In addition, data on the effects of CBT among ethnic minorities are limited. Because Latinos are the largest minority group in the United States, the development of treatments specifically designed for depressed Latino youth are needed. This study will determine whether adding a psychoeducation intervention with parent involvement will be more effective in reducing depressive symptoms among Latino adolescents than treatment with CBT alone.

The treatment phase of this study will last 12 weeks. Participants will be randomly assigned to receive 12 weeks of either CBT alone or CBT with psychoeducation. The psychoeducation will consist of 8 sessions over the 12-week treatment period. During the sessions, participants and their parents will be given detailed information about depression and ways the condition can be treated. They will also be taught coping skills and ways to recognize a relapse. CBT sessions will take place weekly during the study. During the sessions, a therapist will work with participants to modify the behavior and thinking patterns that cause and are associated with their depressive symptoms. Both participants and their parents will undergo interviews at study start, study completion, and 3, 9, and 15 months after study completion. During the interviews, participants' depressive symptoms, school attendance, and overall functional status will be assessed. Parents' stress levels and work attendance will also be assessed. At Months 6 and 12 after study completion, participants and their parents will complete questionnaires to assess any relapses in depressive symptoms.

Study hypothesis: Active treatment with psychoeducation will be superior to no psychoeducation in reducing depression post-treatment. Because the psychoeducation intervention is designed to involve parents and thus impact other aspects of the family system, the treatment is expected to produce better outcomes in several functional domains.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
144 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
None (Open Label)
Official Title:
Parent Psychoeducation Intervention in CBT for Depressed Latino Youth
Study Start Date :
Jul 1, 2004
Anticipated Study Completion Date :
Dec 1, 2008

Outcome Measures

Primary Outcome Measures

  1. General functioning status []

  2. family functioning []

  3. school attendance []

  4. attrition rates []

Eligibility Criteria

Criteria

Ages Eligible for Study:
13 Years to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Diagnosis of depression

  • Parent or guardian willing to provide informed consent

Exclusion Criteria:
  • Psychiatric conditions other than depression

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Center for Psychological Services and Research, University of Puerto Rico San Juan Puerto Rico 00926

Sponsors and Collaborators

  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Guillermo Bernal, PhD, University Center for Psychological Services and Research, University of Puerto Rico

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00118469
Other Study ID Numbers:
  • R01MH067893
  • DSIR 84-CTS
First Posted:
Jul 11, 2005
Last Update Posted:
Apr 3, 2008
Last Verified:
Feb 1, 2008
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 3, 2008