Academic Unit of Psychology, Developmental Brain-Behaviour Laboratory, University of Southampton, Southampton, UK; New York University Child Study Center, New York, and Solent NHS Trust, UK.
Academic Unit of Psychology, Developmental Brain-Behaviour Laboratory, University of Southampton, Southampton, UK; Huntercombe Hospital Maidenhead, Maidenhead, UK.
J Am Acad Child Adolesc Psychiatry. 2016 Jun;55(6):444-55. doi: 10.1016/j.jaac.2016.03.007. Epub 2016 Apr 1.
We performed meta-analyses of randomized controlled trials to examine the effects of neurofeedback on attention-deficit/hyperactivity disorder (ADHD) symptoms and neuropsychological deficits in children and adolescents with ADHD.
We searched PubMed, Ovid, Web of Science, ERIC, and CINAHAL through August 30, 2015. Random-effects models were employed. Studies were evaluated with the Cochrane Risk of Bias tool.
We included 13 trials (520 participants with ADHD). Significant effects were found on ADHD symptoms rated by assessors most proximal to the treatment setting, that is, the least blinded outcome measure (standardized mean difference [SMD]: ADHD total symptoms = 0.35, 95% CI = 0.11-0.59; inattention = 0.36, 95% CI = 0.09-0.63; hyperactivity/impulsivity = 0.26, 95% CI = 0.08-0.43). Effects were not significant when probably blinded ratings were the outcome or in trials with active/sham controls. Results were similar when only frequency band training trials, the most common neurofeedback approach, were analyzed separately. Effects on laboratory measures of inhibition (SMD = 0.30, 95% CI = -0.10 to 0.70) and attention (SMD = 0.13, 95% CI = -0.09 to 0.36) were not significant. Only 4 studies directly assessed whether learning occurred after neurofeedback training. The risk of bias was unclear for many Cochrane Risk of Bias domains in most studies.
Evidence from well-controlled trials with probably blinded outcomes currently fails to support neurofeedback as an effective treatment for ADHD. Future efforts should focus on implementing standard neurofeedback protocols, ensuring learning, and optimizing clinically relevant transfer.
我们对随机对照试验进行了荟萃分析,以检验神经反馈对注意缺陷多动障碍(ADHD)儿童和青少年的 ADHD 症状和神经心理学缺陷的影响。
我们检索了PubMed、Ovid、Web of Science、ERIC 和 CINAHAL,检索时间截至 2015 年 8 月 30 日。采用随机效应模型。使用 Cochrane 偏倚风险工具评估研究。
我们纳入了 13 项试验(520 名 ADHD 患者)。在距离治疗环境最近的评估者评估的 ADHD 症状方面,即最不盲法的结局测量指标上,发现了显著的效果(标准化均数差[SMD]:ADHD 总症状=0.35,95%置信区间[CI]:0.11-0.59;注意力不集中=0.36,95%CI:0.09-0.63;多动/冲动=0.26,95%CI:0.08-0.43)。当采用可能盲法评估或在采用活性/假对照的试验中,结果不显著。当单独分析最常见的神经反馈方法即仅分析频带训练试验时,结果相似。对抑制(SMD=0.30,95%CI:-0.10 至 0.70)和注意力(SMD=0.13,95%CI:-0.09 至 0.36)的实验室测量指标的效果不显著。仅有 4 项研究直接评估了神经反馈训练后是否发生了学习。大多数研究的 Cochrane 偏倚风险多数领域的偏倚风险不明确。
目前,来自采用可能盲法结局的精心对照试验的证据不支持神经反馈是 ADHD 的有效治疗方法。未来的研究应侧重于实施标准的神经反馈方案,确保学习和优化具有临床相关性的转移。