What Four Decades of Meta-Analysis Have Taught Us About Youth Psychotherapy and the Science of Research Synthesis.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2023-05-09 DOI:10.1146/annurev-clinpsy-080921-082920
John R Weisz, Katherine E Venturo-Conerly, Olivia M Fitzpatrick, Jennifer A Frederick, Mei Yi Ng
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引用次数: 1

Abstract

Intervention scientists have published more than 600 randomized controlled trials (RCTs) of youth psychotherapies. Four decades of meta-analyses have been used to synthesize the RCT findings and identify scientifically and clinically significant patterns. These meta-analyses have limitations, noted herein, but they have advanced our understanding of youth psychotherapy, revealing (a) mental health problems for which our interventions are more and less successful (e.g., anxiety and depression, respectively); (b) the beneficial effects of single-session interventions, interventions delivered remotely, and interventions tested in low- and middle-income countries; (c) the association of societal sexism and racism with reduced treatment benefit in majority-girl and majority-Black groups; and, importantly, (d) the finding that average youth treatment benefit has not increased across five decades of research, suggesting that new strategies may be needed. Opportunities for the future include boosting relevance to policy and practice and using meta-analysis to identify mechanisms of change and guide personalizing of treatment.

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四十年的元分析告诉我们关于青少年心理治疗和研究综合科学。
干预科学家已经发表了600多个青少年心理治疗的随机对照试验(rct)。四十年的荟萃分析被用于综合RCT结果,并确定科学和临床意义的模式。本文指出,这些荟萃分析有局限性,但它们促进了我们对青少年心理治疗的理解,揭示了(a)我们的干预措施或多或少成功的心理健康问题(例如,分别是焦虑和抑郁);(b)单次干预措施、远程提供的干预措施以及在低收入和中等收入国家测试的干预措施的有益效果;(c)社会性别歧视和种族主义与多数女孩和多数黑人群体的治疗福利减少有关;而且,重要的是,(d)在50年的研究中发现,青少年治疗的平均收益并没有增加,这表明可能需要新的策略。未来的机会包括提高与政策和实践的相关性,并使用元分析来确定变化机制并指导个性化治疗。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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