Early intervention for youth at high risk for bipolar disorder: A multisite randomized trial of family-focused treatment.
Early intervention for youth at high risk for bipolar disorder: A multisite randomized trial of family-focused treatment.
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DOI:
10.1111/eip.12463
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发表时间:
2019-04
影响因子:
2
通讯作者:
Chang KD
中科院分区:
文献类型:
--
作者:
Miklowitz DJ;Schneck CD;Walshaw PD;Garrett AS;Singh MK;Sugar CA;Chang KD
Despite the considerable public health impact of bipolar disorder (BD), no psychosocial interventions have been systematically evaluated in its early stages. We describe the rationale, design, and analytic methods for a 3-site randomized trial of family-focused treatment for youth at high risk for BD (FFT-HR). Participants (ages 9 to 17 years) have a diagnosis of unspecified BD or major depressive disorder, current mood symptoms, and at least one first- or second-degree relative with a lifetime history of BD I or II. Participants are randomly assigned to FFT-HR (12 sessions in 4 months of family psychoeducation and skills training) or enhanced care (EC; 6 individual and family sessions over 4 months), with pharmacotherapy provided as needed. A subset of participants undergo pre- and post-treatment fMRI scans while performing face-rating and family problem-solving tasks designed to activate corticolimbic circuitry. Independent evaluators assess participants’ status every 4–6 months for up to 4 years. We hypothesize that FFT-HR will be more effective than EC in reducing the severity of mood symptoms (primary outcome) and the hazard of a first manic episode (secondary) over 4 years. Secondarily, we will explore whether FFT-HR is associated with greater decreases in amygdala activation and increases in dorsolateral, ventrolateral, or anterior medial prefrontal cortex activation from pre- to post-treatment. Clinical characteristics of 133 subjects enrolled at baseline are described. This study will test a novel intervention to reduce the early symptoms of BD, and identify neural and behavioral mechanisms that may help refine future treatments. NCT01483391, registered Nov. 26, 2011 at www.clinicaltrials.gov
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影响因子:
5.4
作者:
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通讯作者:
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DOI:
10.1111/j.1469-7610.2010.02210.x
发表时间:
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