The effects of alpha asymmetry and high-beta down-training neurofeedback for patients with the major depressive disorder and anxiety symptoms

lNeurofeedback is a technologically advanced, non-invasive and professional psychological intervention.lBoth ALAY and high-beta down-training neurofeedbacks improved the symptoms of depression and anxiety.lHigh-beta down-training neurofeedback significantly decreased high-beta power in the respectiv...

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Veröffentlicht in:Journal of affective disorders 2019-10, Vol.257, p.287-296
Hauptverfasser: Wang, San-Yu, Lin, I-Mei, Fan, Sheng-Yu, Tsai, Yu-Che, Yen, Cheng-Fang, Yeh, Yi-Chun, Huang, Mei-Feng, Lee, Yu, Chiu, Nien-Mu, Hung, Chi-Fa, Wang, Peng-Wei, Liu, Tai-Ling, Lin, Huang-Chi
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Sprache:eng
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Zusammenfassung:lNeurofeedback is a technologically advanced, non-invasive and professional psychological intervention.lBoth ALAY and high-beta down-training neurofeedbacks improved the symptoms of depression and anxiety.lHigh-beta down-training neurofeedback significantly decreased high-beta power in the respective participants’ electroencephalogram. Alpha-asymmetry neurofeedback (ALAY) was applied to patients with major depressive disorder (MDD) based on the theory of frontal alpha asymmetry. Neurophysiological studies have found a higher high-beta activity of electroencephalography (EEG) at the posterior cortex among patients with comorbid MDD and anxiety symptoms. The present study examined the effects of ALAY and high-beta down-training (Beta) neurofeedback in symptoms of depression and anxiety and EEG parameters. Eighty-seven patients with comorbid MDD and anxiety symptoms were allocated to the ALAY, Beta, or control groups. Both neurofeedback groups received ten-session neurofeedback. All participants completed the Beck Depression Inventory II (BDI-II), Beck Anxiety Inventory (BAI), and five minutes resting EEG recording at pre-test and post-test. EEG raw signals were transformed into an A1 score [log (F4 alpha) - log (F3 alpha)], P3 and P4 high-beta power. BDI-II and BAI scores decreased at post-test in both ALAY and Beta groups, but no significant difference between the two groups. No significant interaction effect in A1 score at pre-test and post-test between the ALAY, Beta, and control groups. The P3 high-beta was significantly decreased in the Beta group, an increase in the control group, and no change in the ALAY group at post-test compared to the pre-test. Both neurofeedback groups decreased symptoms of depression and anxiety. The Beta group was more effective in decreasing high-beta power at the parietal cortex compared to other groups. This non-invasive psychological intervention can be used in the future for patients with comorbid MDD and anxiety symptoms.
ISSN:0165-0327
1573-2517
DOI:10.1016/j.jad.2019.07.026