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| Descriptive Information Fields | |||||||||||||
| Brief Title † | Effectiveness of Family-Focused Treatment Plus Pharmacotherapy for Bipolar Disorder in Adolescents | ||||||||||||
| Official Title † | Family-Focused Treatment for Bipolar Adolescents | ||||||||||||
| Brief Summary | This study will evaluate the effectiveness of family-focused treatment (FFT) plus pharmacotherapy in treating adolescents with bipolar disorder. |
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| Detailed Description | 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. |
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| Study Phase | Phase III | ||||||||||||
| Study Type † | Interventional | ||||||||||||
| Study Design † | Treatment, Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment, Efficacy Study | ||||||||||||
| Primary Outcome Measure † | Time to recovery [ Time Frame: Measured at Month 24 ] Time to recurrence [ Time Frame: Measured at Month 24 ] Severity of manic and depressive symptoms [ Time Frame: Measured at Month 24 ] |
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| Secondary Outcome Measure † | Functioning [ Time Frame: Measured at Month 24 ] Quality of life [ Time Frame: Measured at Month 24 ] Service utilization [ Time Frame: Measured at Month 24 ] |
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| Condition † | Bipolar Disorder | ||||||||||||
| Intervention † | Behavioral: Family-Focused Treatment Plus Pharmacotherapy Behavioral: Enhanced Care Plus Pharmacotherapy |
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| MEDLINE PMIDs | 15571785 | ||||||||||||
| Links | Robert Sutherland Center for the Evaluation and Treatment of Bipolar Disorder, University of Colorado, Boulder ![]() |
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| Recruitment Information Fields | |||||||||||||
| Recruitment Status † | Recruiting | ||||||||||||
| Enrollment † | 150 | ||||||||||||
| Start Date † | August 2006 | ||||||||||||
| Completion Date | April 2011 | ||||||||||||
| Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||||||||||
| Ages | 13 Years to 17 Years | ||||||||||||
| Accepts Healthy Volunteers | No | ||||||||||||
| Contacts †† |
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| Location Countries † | United States | ||||||||||||
| Administrative Information Fields | |||||||||||||
| NCT ID † | NCT00332098 | ||||||||||||
| Organization ID | R01 MH73871 | ||||||||||||
| Secondary IDs †† | R01 MH73817, R01 MH74033, DSIR 84-CTS | ||||||||||||
| Study Sponsor † | National Institute of Mental Health (NIMH) | ||||||||||||
| Collaborators †† | |||||||||||||
| Investigators † |
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| Information Provided By | National Institute of Mental Health (NIMH) | ||||||||||||
| Verification Date | November 2007 | ||||||||||||
| First Received Date † | May 30, 2006 | ||||||||||||
| Last Updated Date | November 21, 2007 | ||||||||||||