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Family Cognitive Behavioral Therapy for Preventing Depression in Children

Vanderbilt University logo

Vanderbilt University

Status

Completed

Conditions

Depression

Treatments

Behavioral: Written Information
Behavioral: Family Group Cognitive Behavioral

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00183482
R01MH100258 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This study will determine the effectiveness of cognitive behavioral therapy (CBT) versus educational treatment in preventing depression in the children of parents with a history of depression.

Full description

Depression is a serious condition that can affect a person's work, relationships, and quality of life. Studies have shown that children of depressed parents are at a higher risk for developing depression than those whose parents have not experienced depression. Safe and effective treatments that can help prevent children of depressed parents from becoming depressed are needed. This study will compare CBT to depression education to determine which is more effective in preventing depression in the children of depressed parents.

Families will be randomly assigned to receive weekly sessions of either CBT or depression education for 12 weeks. Parents in the CBT group will be taught skills to more effectively raise their children and to better manage their depressive symptoms; their children will be taught skills to cope with the stress of their parents' depression. Families in the education group will be informed about the ways that depression can affect individuals with depression and their families.

Study visits will occur at study entry and at Week 12. Several follow-up visits will occur for up to 2 years after the interventional part of the study. At each visit, a clinician will make direct observations of the depressed parent's interaction with his or her children. In addition, families will be interviewed and will complete questionnaires about the parent's depressive symptoms and family interaction.

Enrollment

304 patients

Sex

All

Ages

9+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Participating Families:

  • Families with at least one parent with a history of depression during the life of his or her child
  • Families with at least one child between the age of 10 and 15
  • Parent or guardian willing to provide informed consent for participating children

Exclusion Criteria for All Participants:

  • Parent with bipolar disorder or schizophrenia
  • Child with conduct disorder or pervasive developmental disorder

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

304 participants in 2 patient groups

Family Group Cognitive Behavioral
Experimental group
Description:
The intervention is a family group cognitive behavioral program for families of parents with a history of depression to teach parenting skills to parents and coping skills to children.
Treatment:
Behavioral: Family Group Cognitive Behavioral
Written Information
Active Comparator group
Description:
The comparison arm involves providing written information about depression and stress to parents with a history of depression and their children.
Treatment:
Behavioral: Written Information

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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