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Family Psychoeducation for Children with Mood Disorders - Article


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Nose Disorders

Nasal Disorders


Clinical Trial: Family Psychoeducation for Children with Mood Disorders

This study is no longer recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

The purpose of this study is to evaluate the effectiveness of a Multifamily Psychoeducation Group (MFPG) for the families of children with mood disorders.

Condition Treatment or Intervention Phase
Mood Disorders
 Procedure: Multifamily Psychoeducation Group
Phase I

MedlinePlus related topics:  Mental Health

Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study

Official Title: Family Psychoeducation: Efficacy in Child Mood Disorders

Further Study Details: 

Expected Total Enrollment:  165

Study start: July 2001;  Study completion: June 2006

Mood disorders among youth are a major health concern. Existing mood disorder studies focus on adults, and studies that focus on effective intervention strategies for youth with mood disorders are needed. This 8-session study is an adjunct to ongoing medication management and individual and family psychotherapy for children with mood disorders.

In this study, parents learn about mood disorders, their treatments, and how to work effectively with mental health and school systems. Parents also practice problem-solving and communication skills for symptom management. Children learn about mood disorders and their treatments, including basic cognitive-behavioral principles. Children also learn and practice anger management, problem-solving, and communication skills.

Patients and their families are randomly assigned to 1 of 2 groups. The first group receives 8 sessions of psychoeducation plus treatment as usual (TAU). The second group is a wait-list control in which participants receive only TAU. Patients and caregivers undergo a variety of interviews, tests, and behavioral observations throughout the study. Anxiety, depression, psychosocial stressors, manic symptoms, and children's experiences with psychotropic medications and with treatment or service providers are assessed. Caregivers, teachers, and family friends undergo interviews and make observations of the patient's level of support, general appearance and behavior, and overall functional capacity. The extent to which caregivers agree on the need for treatment and the extent of caregivers' knowledge of mood disorders is also assessed. Assessments occur at 3, 6, 12, 15, and 18 months after study enrollment. A comprehensive assessment is conducted at study entry and 1 year later.

Eligibility

Ages Eligible for Study:  8 Years   -   11 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion criteria:

  • Major depressive disorder, dysthymic disorder, or bipolar disorder (Type I or II)
  • IQ > 70
  • At least 1 parent/caregiver willing to participate in the study
  • Able to attend 6 or more of the 8 treatment sessions with at least 1 parent

Location Information


Ohio
      Ohio State University, Columbus,  Ohio,  43210,  United States

More Information

Study ID Numbers:  61512-01A1
Record last reviewed:  November 2004
Last Updated:  November 12, 2004
Record first received:  December 13, 2002
ClinicalTrials.gov Identifier:  NCT00050557
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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October 11, 2008



Page Updated: September 6, 2005
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