| Literature DB >> 32517043 |
Renata Markiewicz1, Beata Dobrowolska2.
Abstract
The aim of this pilot study was to analyse the influence of Galvanic Skin Response (GSR) Biofeedback training in a group of 18 men with schizophrenia at the remission stage. The results were verified according to: Positive and Negative Syndrome Scale (PANSS), Acceptance of Illness Scale (AIS), Self-efficacy Scale (GSES), Beck Cognitive Insight Scale (BCIS) scales, Colour Trial Test (CTT-1, CTT-2), d2 psychological tests, Quantitative Electroencephalogram (QEEG) Biofeedback, auditory event-related potentials (ERPs), and serum levels of brain-derived neurotrophic factor (BDNF). The results were compared in the same patients after 3 months. Statistically significant changes were noted in results for the variables on the PANSS scale. For the BDNF variable, a statistically significant increase occurred, indicating that GSR Biofeedback training may influence serum levels of the neurotrophic factor. Statistically significant changes were noted in results for the variables on the BCIS, AIS, and GSES indicating an improvement in the cognitive and social functioning. Changes were noted for results for theta/beta and theta/Sensory Motor Rhythm (SMR) ratios, which indicate an improvement in concentration and attention. Changes were noted for the N1 wave amplitude in the frontal brain region (F-z), and for the P2 wave latency in the central brain region (C-z), which indicates an improvement in the initial perceptual analysis. The use of GSR Biofeedback in a group of patients with schizophrenia gives interesting results, but requires further in-depth research.Entities:
Keywords: QEEG Biofeedback; event-related potentials (ERP); schizophrenia; serum neurotrophic factor (BDNF)
Year: 2020 PMID: 32517043 PMCID: PMC7312635 DOI: 10.3390/ijerph17114034
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Comparative analysis of results obtained before therapy (Examination 1) and after therapy (Examination 2); latency (latency time in ms), and amplitude (mv, peak-to-peak).
| Variable | Examination 1 | Examination 2 | Difference | Significance of Differences | Confidence Level | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| M | SD | CV% | M | SD | CV% | T |
| −95% | +95% | ||
| PANSS-POS | 9.06 | 2.04 | 22.52 | 7.50 | 2.23 | 29.73 | −1.56 | 10.719 | <0.001 | −1.86 | −1.25 |
| PANSS-NEG | 13.94 | 3.92 | 28.12 | 11.83 | 4.48 | 37.87 | −2.11 | 8.304 | <0001 | −2.65 | −1.57 |
| PANSS-GEN | 24.83 | 3.35 | 13.49 | 22.61 | 3.71 | 16.41 | −2.22 | 10.736 | <0001 | −2.66 | −1.79 |
| PANSS-TOT | 47.83 | 8.49 | 17.75 | 41.94 | 9.64 | 22.99 | −5.89 | 11.834 | <0001 | −6.94 | −4.84 |
| BDNF | 44.78 | 10.69 | 23.87 | 55.50 | 10.76 | 19.39 | 10.72 | −6.185 | <0001 | 7.06 | 14.38 |
| BCISS | 22.72 | 4.80 | 21.13 | 25.72 | 3.14 | 12.21 | 3.00 | −3.170 | 0.006 | −5.00 | −1.00 |
| AIS | 22.67 | 8.95 | 39.48 | 26.44 | 6.46 | 24.43 | 3.78 | −2.547 | 0.021 | 0.65 | 6.91 |
| GSES | 23.78 | 5.43 | 22.83 | 27.61 | 5.09 | 18.44 | 3.83 | −3.239 | 0.005 | 1.34 | 6.33 |
| QEEG C-z theta/beta | 1.92 | 0.57 | 29.69 | 2.29 | 0.88 | 38.43 | 0.37 | −2.632 | 0.018 | 0.07 | 0.67 |
| QEEG C-z theta/SMR | 2.07 | 0.64 | 30.92 | 2.37 | 0.80 | 33.76 | 0.30 | −2.358 | 0.031 | 0.03 | 0.57 |
| F-z N1 (amplitude) | −3.95 | 2.53 | 64.05 | −5.36 | 1.93 | 36.01 | −1.41 | 2.588 | 0.020 | −2.57 | −0.26 |
| C-z P2 (latency) | 208.8 | 14.81 | 7.09 | 196.1 | 18.27 | 9.32 | −12.77 | 2.643 | 0.018 | −23.01 | −2.52 |
M—mean value; SD—standard deviation; CV%—coefficient of variation; T—Student’s t-test; p—level of significance PANSS-POS—Positive and Negative Syndrome Scale—POSITIVE; PANSS-NEG—Positive and Negative Syndrome Scale—NEGATIVE; PANSS-GEN—Positive and Negative Syndrome Scale—GENERAL; PANSS-TOT—Positive and Negative Syndrome Scale—TOTAL; BDNF—brain derived neurotrophic factor; BCISS—Beck Cognitive Insight Scale; AIS—Acceptance of Illness Scale; GSES—Self-efficacy Scale; QEEG C-z theta/beta—attention factor of the central area; QEEG C-z theta/SMR—concentration factor of the central area; F-z N1 (amplitude)—amplitude of the first negative component of the central area; C-z P2 (latency—delay of the second positive component of the central area.