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预防高危青少年抑郁症:一项随机对照试验。

Prevention of depression in at-risk adolescents: a randomized controlled trial.

作者信息

Garber Judy, Clarke Gregory N, Weersing V Robin, Beardslee William R, Brent David A, Gladstone Tracy R G, DeBar Lynn L, Lynch Frances L, D'Angelo Eugene, Hollon Steven D, Shamseddeen Wael, Iyengar Satish

机构信息

Department of Psychology and Human Development, Vanderbilt University, 552 Peabody, 230 Appleton Pl, Nashville, TN 37203-5721, USA.

出版信息

JAMA. 2009 Jun 3;301(21):2215-24. doi: 10.1001/jama.2009.788.

Abstract

CONTEXT

Adolescent offspring of depressed parents are at markedly increased risk of developing depressive disorders. Although some smaller targeted prevention trials have found that depression risk can be reduced, these results have yet to be replicated and extended to large-scale, at-risk populations in different settings.

OBJECTIVE

To determine the effects of a group cognitive behavioral (CB) prevention program compared with usual care in preventing the onset of depression.

DESIGN, SETTING, AND PARTICIPANTS: A multicenter randomized controlled trial conducted in 4 US cities in which 316 adolescent (aged 13-17 years) offspring of parents with current or prior depressive disorders were recruited from August 2003 through February 2006. Adolescents had a past history of depression, current elevated but subdiagnostic depressive symptoms, or both. Assessments were conducted at baseline, after the 8-week intervention, and after the 6-month continuation phase.

INTERVENTION

Adolescents were randomly assigned to the CB prevention program consisting of 8 weekly, 90-minute group sessions followed by 6 monthly continuation sessions or assigned to receive usual care alone.

MAIN OUTCOME MEASURE

Rate and hazard ratio (HR) of a probable or definite depressive episode (ie, depressive symptom rating score of > or = 4) for at least 2 weeks as diagnosed by clinical interviewers.

RESULTS

Through the postcontinuation session follow-up, the rate and HR of incident depressive episodes were lower for those in the CB prevention program than for those in usual care (21.4% vs 32.7%; HR, 0.63; 95% confidence interval [CI], 0.40-0.98). Adolescents in the CB prevention program also showed significantly greater improvement in self-reported depressive symptoms than those in usual care (coefficient, -1.1; z = -2.2; P = .03). Current parental depression at baseline moderated intervention effects (HR, 5.98; 95% CI, 2.29-15.58; P = .001). Among adolescents whose parents were not depressed at baseline, the CB prevention program was more effective in preventing onset of depression than usual care (11.7% vs 40.5%; HR, 0.24; 95% CI, 0.11-0.50), whereas for adolescents with a currently depressed parent, the CB prevention program was not more effective than usual care in preventing incident depression (31.2% vs 24.3%; HR, 1.43; 95% CI, 0.76-2.67).

CONCLUSION

The CB prevention program had a significant prevention effect through the 9-month follow-up period based on both clinical diagnoses and self-reported depressive symptoms, but this effect was not evident for adolescents with a currently depressed parent.

TRIAL REGISTRATION

clinicaltrials.gov Identifier: NCT00073671.

摘要

背景

父母患有抑郁症的青少年患抑郁症的风险显著增加。尽管一些规模较小的针对性预防试验发现抑郁症风险可以降低,但这些结果尚未得到重复验证,也未扩展到不同环境中的大规模高危人群。

目的

确定团体认知行为(CB)预防计划与常规护理相比在预防抑郁症发作方面的效果。

设计、地点和参与者:在美国4个城市进行的一项多中心随机对照试验,2003年8月至2006年2月招募了316名父母患有当前或既往抑郁症的青少年(13 - 17岁)。这些青少年有抑郁症病史、当前抑郁症状升高但未达到诊断标准,或两者皆有。在基线、8周干预后以及6个月延续期后进行评估。

干预措施

青少年被随机分配到CB预防计划,该计划包括8次每周90分钟的团体课程,随后是6次每月的延续课程,或仅接受常规护理。

主要结局指标

临床访谈者诊断的至少持续2周的可能或确定的抑郁发作(即抑郁症状评分≥4)的发生率和风险比(HR)。

结果

通过延续期后的随访,CB预防计划组的抑郁发作发生率和HR低于常规护理组(21.4%对32.7%;HR,0.63;95%置信区间[CI],0.40 - 0.98)。CB预防计划组青少年自我报告的抑郁症状改善也显著大于常规护理组(系数,-1.1;z = -2.2;P = 0.03)。基线时父母当前的抑郁症对干预效果有调节作用(HR,5.98;95%CI,2.29 - 15.58;P = 0.001)。在基线时父母未患抑郁症的青少年中,CB预防计划在预防抑郁症发作方面比常规护理更有效(11.7%对40.5%;HR,0.24;95%CI,0.11 - 0.50),而对于父母当前患有抑郁症的青少年,CB预防计划在预防新发抑郁症方面并不比常规护理更有效(31.2%对24.3%;HR,1.43;95%CI, 0.76 - 2.67)。

结论

基于临床诊断和自我报告的抑郁症状,CB预防计划在9个月的随访期内有显著的预防效果,但对于父母当前患有抑郁症的青少年,这种效果并不明显。

试验注册

clinicaltrials.gov标识符:NCT00073671。

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