Pooled patient-level meta-analysis of children and adults completing a computer-based anxiety intervention targeting attentional bias.
Pooled patient-level meta-analysis of children and adults completing a computer-based anxiety intervention targeting attentional bias.
复制标题
对完成针对注意力偏差的基于计算机的焦虑干预的儿童和成人进行汇总患者水平荟萃分析。
DOI:
10.1016/j.cpr.2016.09.009
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发表时间:
2016-12
影响因子:
12.8
通讯作者:
Bar-Haim, Yair
中科院分区:
文献类型:
--
作者:
Price, Rebecca B.;Wallace, Meredith;Kuckertz, Jennie M.;Amir, Nader;Graur, Simona;Cummings, Logan;Popa, Paul;Carlbring, Per;Bar-Haim, Yair
关键词:
Computer-based approaches, such as Attention Bias Modification (ABM), could help improve access to care for anxiety. Study-level meta-analyses of ABM have produced conflicting findings and leave critical questions unresolved regarding ABM’s mechanisms of action and clinical potential. We pooled patient-level datasets from randomized controlled trials of children and adults with high-anxiety. Attentional bias (AB) towards threat, the target mechanism of ABM, was tested as an outcome and a mechanistic mediator and moderator of anxiety reduction. Diagnostic remission and Liebowitz Social Anxiety Scale (LSAS) were clinical outcomes available in enough studies to enable pooling. Per-patient data were obtained on at least one outcome from 13/16 eligible studies [86% of eligible participants; n=778]. Significant main effects of ABM on diagnostic remission (ABM—22.6%, control—10.8%; OR=2.57; p=.006) and AB (β*(95%CI)=−.63(−.83, −.42); p<.00005) were observed. There was no main effect of ABM on LSAS. However, moderator analyses suggested ABM was effective for patients who were younger (≤37y), trained in the lab, and/or assessed by clinicians. Under the same conditions where ABM was effective, mechanistic links between AB and anxiety reduction were supported. Under these specific circumstances, ABM reduces anxiety and acts through its target mechanism, supporting ABM’s theoretical basis while simultaneously suggesting clinical indications and refinements to improve its currently limited clinical potential.
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影响因子:
6.9
作者:
Fresco, DM;Coles, ME;Goetz, D
通讯作者:
Goetz, D
影响因子:
10.6
作者:
Hakamata, Yuko;Lissek, Shmuel;Bar-Haim, Yair;Britton, Jennifer C.;Fox, Nathan A.;Leibenluft, Ellen;Ernst, Monique;Pine, Daniel S.
通讯作者:
Pine, Daniel S.
影响因子:
3.7
作者:
Boettcher J;Leek L;Matson L;Holmes EA;Browning M;MacLeod C;Andersson G;Carlbring P
通讯作者:
Carlbring P
影响因子:
3.7
作者:
Beard C;Sawyer AT;Hofmann SG
通讯作者:
Hofmann SG
影响因子:
5.3
作者:
Greenberg, PE;Sisitsky, T;Fyer, AJ
通讯作者:
Fyer, AJ