TREAMENT OF EARLY AGE MANIA (TEAM)

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 本研究的总体目的是对6.0-15岁（N=540）患有DSM-IV（躁狂或混合期）或躁狂的患者进行协作性、多中心精神药理学有效性研究。 本方案的具体目的是：（1）研究锂、丙戊酸盐和利培酮作为单药治疗和作为添加药物治疗儿童BP-1（躁狂或混合相）障碍的有效性（2）试验一种复杂的、多层次的适应性策略设计（3）探索心理社会因素对停药、依从性和结局的影响。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The overall aim of this study is to perform a collaborative, multisite psychopharmacology effectiveness study of 6.0-15 years old (N=540) who have DSM-IV (mania or mixed phase) or mania. The specific aims of this protocol are: (1) To investigate the effectivness of lithium, valproate and resperidone as monotherapy and as add-on agents for childhood BP-1 (manic or mixed phase) disorder (2) To pilot a complex, multistrata, adaptive strategy design (3) to explore the effects of psychosocial factors on discontinuation, compliance and outcome.