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Effectiveness of Family-Focused Treatment Plus Pharmacotherapy for Bipolar Disorder in Adolescents
This study is currently recruiting participants.
Study NCT00332098   Information provided by National Institute of Mental Health (NIMH)
First Received: May 30, 2006   Last Updated: March 10, 2009   History of Changes

May 30, 2006
March 10, 2009
August 2006
April 2011   (final data collection date for primary outcome measure)
  • Time to recovery [ Time Frame: Measured at Month 24 ] [ Designated as safety issue: No ]
  • Time to recurrence [ Time Frame: Measured at Month 24 ] [ Designated as safety issue: No ]
  • Severity of manic and depressive symptoms [ Time Frame: Measured at Month 24 ] [ Designated as safety issue: No ]
  • Measured at Month 24: Time to recovery
  • Time to recurrence
  • Severity of manic and depressive symptoms
Complete list of historical versions of study NCT00332098 on ClinicalTrials.gov Archive Site
  • Functioning [ Time Frame: Measured at Month 24 ] [ Designated as safety issue: No ]
  • Quality of life [ Time Frame: Measured at Month 24 ] [ Designated as safety issue: No ]
  • Service utilization [ Time Frame: Measured at Month 24 ] [ Designated as safety issue: No ]
  • Measured at Month 24: Functioning
  • Quality of Life
  • Service Utilization
 
Effectiveness of Family-Focused Treatment Plus Pharmacotherapy for Bipolar Disorder in Adolescents
Family-Focused Treatment for Bipolar Adolescents

This study will evaluate the effectiveness of family-focused treatment (FFT) plus pharmacotherapy in treating adolescents with bipolar disorder.

Bipolar disorder (BPD) is a serious mental illness that causes drastic shifts in a person's mood, energy, and ability to function. BPD can strike at any age, but it most commonly develops in late adolescence or early adulthood. The disorder is characterized by alternating episodes of mania and depression, often with periods of normal mood in between. Some symptoms of a manic episode include the following behaviors: increased energy, activity, and restlessness; excessively "high," overly good, euphoric mood; and extreme irritability. In contrast, a depressive episode is characterized by a lasting sad, anxious, or empty mood; feelings of hopelessness or pessimism; and decreased energy. Adolescents with BPD have high rates of disease recurrence, suicide attempts, functional impairment, and mental health service utilization, even with aggressive treatment with mood stabilizers and antipsychotic drugs. Research has suggested that FFT, a behavioral intervention consisting of psychoeducation, communication training, and problem solving training, may lead to improvements in BPD symptoms in adolescents. This study will evaluate the effectiveness of FFT plus pharmacotherapy in treating adolescents with BPD.

Participants in this 2-year, single-blind study will be randomly assigned to receive a combination of either FFT and pharmacotherapy or enhanced care (EC) and pharmacotherapy. Medications used for the pharmacotherapy portion of the study will include mood stabilizers, such as lithium or divalproex sodium, and atypical antipsychotics, such as quetiapine. Participants will also receive anti-anxiety medications, psychostimulants, or antidepressants as needed. All participants will receive pharmacotherapy for the full 2 years. Participants assigned to EC will take part in weekly brief psychoeducation sessions for 3 weeks. Participants assigned to FFT will take part in weekly treatment sessions with their families for 12 weeks, biweekly for 12 weeks, monthly for 3 months, and then trimonthly until Month 24. Both FFT and EC treatment sessions will include psychoeducation focusing on appropriate ways to manage BPD and its cycling nature. Crisis intervention sessions will also be offered to all participants on an as-needed basis for the duration of the study. Outcomes, including BPD symptoms, functioning, and service utilization, will be measured at study visits at Months 3, 6, 9, 12, 18, and 24.

Phase III
Interventional
Treatment, Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment, Efficacy Study
Bipolar Disorder
  • Behavioral: Family-Focused Treatment Plus Pharmacotherapy
  • Behavioral: Enhanced Care Plus Pharmacotherapy
  • Experimental: Family-Focused Treatment Plus Pharmacotherapy
  • Active Comparator: Enhanced Care Plus Pharmacotherapy

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
150
April 2011
April 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Between the ages of 13 years, 0 months and 17 years, 11 months
  • Meets DSM-IV-TR criteria for either of the following conditions: bipolar I or bipolar II disorder with a manic, mixed, or hypomanic episode within 3 months of study entry; or a depressed episode within 3 months of study entry with a prior history of a manic, hypomanic, or mixed episode (if the participant only meets criteria for a current hypomanic episode, there must also be a history of at least one prior depressive, manic, or mixed episode)
  • Has experienced severe depression, hypomania, or mania symptoms for a period of at least 1 week within the 3 months prior to study entry
  • Lives with at least one biological or step-parent who is available and willing to participate in treatment (parents not currently living with the adolescent participant may also participate)

Exclusion Criteria:

  • Currently in full recovery (experienced minimal symptoms for at least 8 continuous weeks)
  • Meets DSM-IV criteria for substance abuse disorder or substance dependence disorder within 3 months of study entry (based on the Kiddie Schedule for Affective Disorders and Schizophrenia - Present and Lifetime Version [KSADS-PL])
  • Meets current criteria for bipolar, not otherwise specified, or substance-induced mood disorder
  • Diagnosis of mental retardation (as defined by an IQ less than 70), autism, or organic central nervous system disorder
  • Severe, unremitting psychosis that is unresponsive to neuroleptic medications, and has lasted more than 3 months
  • Requires extended inpatient treatment (although participant can be hospitalized at the time of intake into the study)
  • Current life-threatening eating disorder, neurological condition, or other medical problem that requires immediate treatment
  • Exhibits or expresses serious homicidal tendencies
  • Victim of current sexual or physical abuse by parents or is in an environment marked by domestic violence among the parents or step-parents
Both
13 Years to 17 Years
No
Contact: David J. Miklowitz, PhD 303-492-8575 miklow@psych.colorado.edu
Contact: Elizabeth L. George, PhD 303-207-1161 egeorge@colorado.edu
United States
 
NCT00332098
David J. Miklowitz, PhD, University of Colorado, Dept. of Psychology
R01 MH073871, R01 MH73817, R01 MH74033, DSIR 84-CTS
National Institute of Mental Health (NIMH)
 
Principal Investigator: David J. Miklowitz, PhD University of Colorado at Boulder
Principal Investigator: Robert A. Kowatch, MD University of Cincinnati
Principal Investigator: David A. Axelson, MD University of Pittsburgh
National Institute of Mental Health (NIMH)
March 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP