Abstract
Background
Brain relaxation is attained using several techniques while sleep remains nature’s ultimate remedy. Currently, various machine learning (ML) tools are applied to identify and understand the neural correlates of relaxation from the electroencephalography (EEG) signals. Majority of earlier studies focused on comparing power in the EEG bands during eyes-open and eyes-closed resting state paradigm to train the datasets. However, several Yogic practices are performed using sitting and supine positions.
Purpose
This study was aimed to elucidate the relaxation correlates in EEG between supine and sitting position during eyes-closed condition using ML classifiers.
Methods
EEG signals were recorded on five different days from O1, OZ, O2, C3, CZ, C4, F3, FZ and F4 brain region using nine unipolar electrodes for 25 minutes during eyes-closed supine and eyes-closed sitting postures each on, along with electrocardiogram (ECG) for heart rate variability (HRV) analysis in a healthy participant. Relaxation was assessed by extracting the relative power of the alpha and theta waves from the EEG data and corroborated with the alpha and theta lateralisation index (LI) and HRV parameters. These EEG metrics were analysed by leveraging ML classifiers (K-nearest neighbours (KNN), support vector machine(SVM), random forest (RF) and XGBoost) for relaxation states under sitting and supine states.
Results
Out of all the used classifiers, performance indices of SVM excelled in classifying relaxation states from the EEG alpha and theta band data that was verified with the HRV data and correlated with LI.
Conclusion
This study demonstrates that ML especially the SVM was effective in classifying the relaxation states during different postures from the EEG. LI and HRV metrics effectively decoded the underlying message in the EEG and ECG respectively.
Keywords: Electroencephalogram, relaxation, alpha waves, theta waves, heart rate variability, machine learning, support vector machine
Introduction
Hans Berger’s cardinal recording of human electroencephalography (EEG) for the first time in 1924 unlocked the avenues for gaining insight into functionality of brain.1, 2 Observation of alpha waves (Berger’s wave) in the resting state was historical for evoking interest in decoding the underlying message in EEG activity but the pace of research remained slow during initial four to five decades probably due to the limited availability of EEG machines at that time. However, technological advancement in the twenty-first century with digitisation, compact miniaturised machines, increased computational power and application of artificial intelligence (AI) and machine learning (ML) and EEG is becoming an important noninvasive and extensively used technique for recording electrical activities from various cortical areas of brain in clinical and research domains including consciousness, sleep diagnosis, neurological disorders, understanding various cognitive processes and overall well-being.3–12
EEG is a complex signal consisting of different frequency bands with distinct functional connotations, for example, delta (0.1–3Hz) for deep sleep, basic homeostatic and motivational processes; theta (4–7 Hz) for drowsiness and meditation; alpha (8–13 Hz) for relaxed wakefulness; beta (14–30 Hz) for active thinking and concentration and gamma (30–60 Hz) for high-level cognitive functions as shown in Table 1. One of the growing concerns in the recent lifestyles is a global increase in insomnia and sleep disorders in all age groups that is associated with concomitant surge in cardiovascular diseases, hypertension, anxiety, depression, cancer and neurodegenerative disorders.13–16 It is pointed that optimal sleep each night provides natural relaxation and recuperation of the body and mind but that is a hard challenge. Various relaxation techniques including Yoga and biofeedback are becoming hope for the management of these health issues.
Table 1. Characteristics of the Frequency Bands in the EEG from Various Areas of Brain.
| Band | Frequency (Hz) | Characteristics | Locations |
| Delta | 0.1–3 | Deep sleep, unconsciousness | Frontally in adults, posteriorly in children |
| Theta | 4–7 | Drowsiness, relaxation, dreaming | Medial temporal lobe |
| Alpha | 8–13 | Relaxed wakefulness, meditation | Posterior regions of the head |
| Beta | 14–30 | Active thinking, concentration | Frontal lobe and motor cortex |
| Gamma | 30–60 | High cognitive activity | Somatosensory cortex |
Observation of notable increase in alpha waves in the occipital region during relaxation is a hallmark of attaining a calm and restful brain state.17, 18 Alpha power decreases during attention tasks compared to the relaxed state, particularly in the frontal and occipital regions of the brain, so the changes in alpha power can be a significant marker for distinguishing between states of relaxation and attention. 19 Theta wave activity is also often associated with drowsiness or light meditation. Conversely, alpha wave activity decreases when the eyes are open, while beta wave activity increases during alertness and cognitive engagement. The regional distribution and dominance of these individual EEG waveforms in different lobes contribute to various neural processing involved in specific functional and cognitive domains, for example, the frontal lobe in decision-making, the parietal lobe in sensory and spatial orientation, the temporal lobe auditory processing and memory and the occipital lobe for visual processing.20, 21 Hemispheric lateralisation is an interesting dimension of EEG neural processing especially for the alpha lateralisation as it enhances the processing of stimuli at relevant spatial locations while suppressing distractors.22–25 Even though no specific attentive task was planned in this study but it would be interesting to observe any changes in alpha lateralisation in resting state.
ML is a subset of AI that is broadly categorised into supervised, unsupervised or reinforced learning. In the supervised learning, the labelled dataset is used to train the algorithm for predicting the outcomes while in the unsupervised ML, the machine algorithm learns itself by identifying the patterns in the unlabelled data. In the reinforced learning technique, machine learns through trial and error as the agent learns to derive decisions by interacting with environment, and refine at each step to reach a goal. In recent years, there is surge in application of ML tool for the assessment of the neural correlates of relaxation from the EEG recordings. However, most of the studies have employed supervised ML techniques using eyes-open (EO) versus eyes-closed (EC) paradigm in the resting state (Table 2).26–32 It is pointed that the relaxation practices are conducted in both sitting and supine positions 33 but such studies are scarce. Heart rate variability (HRV) is another clinical tool that is computed from the beat-to-beat changes in the HR. It is a valuable indicator of the autonomic nervous system activity, providing a comprehensive view of sympathetic and parasympathetic balance of the body during rest and stress.34–36 Thus, this study was aimed to classify relaxation states from EEG marker (alpha and theta waves) acquired in different postures (supine and sitting position) in EC condition using ML classifiers. By combining EEG and HRV data, we aimed to deepen our understanding of relaxation across different postures through ML tools as it would be helpful in optimising relaxation techniques for clinical and therapeutic use. To accurately classify relaxation states, ML algorithms like random forest (RF), support vector machine (SVM), K-nearest neighbours (KNN) and XGBoost were used to analyse the EEG data.
Table 2. Results of Previous Studies Classifying Mental States Using EEG Under Eyes Open (EO) Versus Eyes Closed (EC) Conditions.
| Study Group | Subject Details | Protocol | Classifiers Used | Classification Accuracy |
| Alipoor et al., 2009 26 |
N = 5 Healthy participants, epileptic patients |
Resting state EO, EC | ANN | ANN: 98.02% |
| Sinha and Babu, 2016 27 |
N = 109 Healthy participants |
EO, EC | SVM RBF Kernel KNN (k = 7) | SVM RBF: 76.19% KNN: 76.60% |
| Saidatul et al., 2011 28 |
N = 5 Healthy male |
Resting state in mental arithmetic task | ANN | Burg-Method: 91.17% Welch: 88.36% Yule-Walker: 85.55% |
| Laport et al., 2020 29 |
N = 7 Healthy males |
EO, EC Feature extraction: DFT |
SVMLDA | EO - SVM: 89.04%–99.88% LDA: 70.12%–97.71% EC -SVM: 87.83%–100.00% LDA: 89.88%–100.00% |
| Mahato and Paul, 2020 30 |
N = 60 Healthy participants, MDD patients |
EC resting state | SVM | SVM: 88.33% |
| Mattiev et al., 2023 31 |
N = 50 Healthy participants |
Resting state with EC, EO | Opt. Ensemble | Opt. Ensemble: CP50: 98.3%, SP50:99.0% |
| Kan et al., 2017 32 | N = 29 Healthy participants | Resting state: EC & EO | Stepwise LDA | LDA: 86.2% |
Notes: DFT, discrete Fourier transform; Burg, Burg-parametric spectral estimation; Welch, Welch-averaged periodograms; Yule-Walker, Autoregressive estimation; ANN, artificial neural network; SVM RBF, support vector machine-radial basis function; KNN, K-nearest neighbours; LDA, linear discriminant analysis; Opt. ensemble, optimised ensemble classifier; CP50, fully preprocessed data (50 subjects); SP50, basic preprocessed data (50 subjects).
Methods
Participant
After taking informed consent, the data were acquired from healthy right-handed subject on five different days in this study. The experimental protocol involved recording EEGs from different parts of brain using nine unipolar electrodes along with ECG under two conditions: (a) 25 minutes in a supine posture with EC and (b) 25 minutes sitting with EC in a quiet air-conditioned room using the 32-channel EEG device. The subject was asked not to get into sleep. For this study, the Institutional Ethics Committee (SCT/IEC/2074/AUGUST/2023) of Sree Chitra Tirunal Institute for Medical Sciences & Technology approval was taken.
Measures
The data was acquired using the Axxonet XAmp 32-channel EEG system (Axxonet system Technologies Pvt Ltd, Bangalore, Karnataka, India) with a sampling rate of 256 Hz and a bandpass filter of 0.2–35 Hz. For recording EEGs, nine unipolar electrodes (O1, OZ, O2, C3, CZ, C4, F3, FZ, F4) were placed on scalp according to the international 10–20 system (Figure 1) and additional two ECG electrodes were placed to record HR. BESS (Brain Electro Scan Software) was used to preprocess EEG data for removing the noise and artifacts. The fast Fourier transform (FFT) was performed on these noise-free signals to extract the relative power of theta (4–7 Hz) and alpha (8–12 Hz) waves taking one-second bins.
Figure 1. International 10-20 EEG Electrode Placement System.

Note: O1, Left Occipital Lobe; O2, Right Occipital Lobe; Oz, Occipital Midline; C3, Left Central Lobe; CZ, Central Midline; C4, Right Central; F3, Left Frontal Lobe; FZ, Frontal Midline; F4, Right Frontal.
For the ECG signals, Kubios HRV software was utilised to analyse HRV taking five minutes epoch length to obtain insights into the sympathetic and parasympathetic balance during each state. Time domain parameters (mean RR, mean HR, min HR, max HR) and frequency domain parameters (low-frequency (LF) power, high-frequency (HF) power) and LF/HF ratios) were extracted.
Data Processing and Machine Learning
Python 3.10 was used along with libraries such as NumPy, pandas, SciPy, seaborn, matplotlib, stats models, Plotly and sci-kit-learn for data curation, feature selection, exploratory data analysis, statistical analysis and model training. The study employed RF, SVM, KNN and XGBoost to classify relaxation postures. RF, SVM, KNN and XGBoost algorithms were used to classify postures based on the features derived from EEG data. Twenty per cent of the data was used for testing, while 80% was used for training. The features included relative power from all unipolar channels, and the target variable was posture (0 for sitting, 1 for supine).
ML Evaluation Parameters and Statistical Methods
Performance of the classifiers were evaluated using confusion matrix, accuracy, precision, recall, specificity, F1 score and area under the curve (AUC) and receiver operating characteristic (ROC) curves as described below:
Confusion matrix to display true positive (TP), true negative (TN), false positive (FP) and false negative (FN); Accuracy: The proportion of correct predictions (TP + TN) out of all predictions; Precision: The proportion of TPs out of all positive predictions = TP/ (TP + FP); Recall: The proportion of TPs out of actual positives = (TP/ (TP + FN); Specificity: The proportion of TNs out of actual negatives = TN/ (TN + FP); F1 Score: The harmonic mean of Precision and Recall. AUC: to measures overall performance across classification thresholds. ROC curve were also checked to compare TP rate versus FP rate.
Lateralisation index (LI) was calculated for alpha and theta power in each channel (C, O, F) by using formula (Ipsilateral power – Contralateral power/Ipsilateral power + Contralateral power) and comparison was carried out between sitting and supine state for each individual area. 25 For the ECG signals, Kubios HRV software was utilised to analyse HRV taking five minutes epoch length to obtain insights into the sympathetic and parasympathetic balance during each state. Time domain parameters (mean RR, mean HR, min HR, max HR) and frequency domain parameters (LF power, HF power) and LF/HF ratios were extracted. These data were analysed using GraphPad PRISM software (version 10). Analysis of variance (ANOVA) and t-tests were conducted to assess differences in relaxation levels between conditions to doubly check the performance of ML. Level of significance was taken as 0.05.
Results
For classifying relaxation states based on the EEG data, ML models for KNN, RF, SVM and XGBoost were evaluated. For the alpha relative power, SVM achieved the highest accuracy of 84.98% and precision of 89.75%, with an AUC of 93.19% (Table 3). For theta relative power, SVM has the highest accuracy of 74.29% and AUC 81.58% in Table 4.
Table 3. Comparison of Performance Indices for Various Classifiers for Relative Power of Alpha Waves.
| Classifier | Accuracy | Precision | Recall | F1 Score | AUC | Specificity |
| RF | 0.848 | 0.878 | 0.846 | 0.861 | 0.930 | 0.852 |
| SVM | 0.851 | 0.892 | 0.833 | 0.862 | 0.933 | 0.873 |
| KNN | 0.822 | 0.842 | 0.840 | 0.841 | 0.905 | 0.800 |
| XGBoost | 0.839 | 0.858 | 0.853 | 0.856 | 0.930 | 0.822 |
Table 4. Comparison of Performance Indices for Various Classifiers for Relative Power of Theta Waves.
| Classifier | Accuracy | Precision | Recall | F1 Score | AUC | Specificity |
| RF | 0.722 | 0.695 | 0.572 | 0.627 | 0.795 | 0.826 |
| SVM | 0.732 | 0.727 | 0.569 | 0.638 | 0.803 | 0.852 |
| KNN | 0.699 | 0.642 | 0.593 | 0.617 | 0.756 | 0.771 |
| XGBoost | 0.717 | 0.681 | 0.578 | 0.625 | 0.792 | 0.813 |
The ROC curves and AUC values showed that all models performed well in classifying brain activity for both alpha and theta power. For alpha power, performance of the SVM model was highest with an AUC of 0.933, indicating it could distinguish between different states very effectively. XGBoost and RF were close behind, each with an AUC of 0.931 and 0.930, proving to be reliable, while KNN, with an AUC of 0.906 (Figure 2A).
Figure 2. Receiver Operating Characteristic Curve of All Classifiers to Classify Relaxation State Using Relative Alpha Power (A) and Theta Power (B).

For theta power, SVM performed better with an AUC of 0.804, showing it could pick up differences between states well. RF and XGBoost followed with AUCs of 0.795 and 0.793 respectively and KNN, with an AUC of 0.793, also performed decently (Figure 2B). Overall, the high AUC values across all models suggest they are effective at this task, with SVM standing out as the top performer, especially in recognising subtle changes in brain activity.
Among various ML models evaluated for classifying relaxation states using EEG data, SVM stood out as the most effective classifier for alpha and theta relative power (Tables 2 and 3; Figure 2). Both models achieved the highest AUC values of 0.933 for alpha power, highlighting their superior discriminative abilities. In theta power classification, SVM had also led with AUC values of 0.804. Overall, SVM demonstrated the best balance of precision, recall and AUC, establishing them as the top choices for EEG-based relaxation state classification.
Changes in the relative power of alpha and theta EEG waves from different regions of brain were analysed under two different states EC supine and EC sitting postures (Figure 3). In the supine posture, relative alpha power of EEG was significantly higher in all the recorded regions in comparison to sitting state (Figure 3A). Highest changes in alpha power were evident in the occipital channels (O1, OZ, O2) compared to other channels, whereas lowest change was observed in the CZ channel (p < .05) as depicted in Figure 3A.
Figure 3. Changes in EEG Alpha (A) and Theta (B) Relative Powers in Different Parts of the Brain During EC Supine and EC Sitting Positions.

Note: Mean Relative Power of Alpha, Theta and Standard Error in the Y Axis and EEG Channels on the X Axis Where O Is Occipital, C Is Central and F Is Frontal. The Level of Significance Is Depicted as *p ≤ .05, *** p ≤ .001.
It is noted that the overall relative EEG theta power was lower than the alpha powers during both these EC states (Figure 3). Within recorded brain areas, significant increases in theta powers were found in the occipital channels O1 (p < .05), OZ, central and frontal area (p < .001) and during the supine posture (Figure 3B).
The LI for alpha power band significantly decreased in the occipital and frontal regions, while it increased for the theta power band during transition from the EC supine to EC sitting posture (Figure 4). LI was negative in central region for alpha band, occipital and frontal region for theta band without showing any significant changes between supine to sitting state.
Figure 4. Comparison of Lateralisation Index for EEG Alpha (A) and Theta (B) Waves Between Supine and Sitting Position in Eyes Closed State.

Note: Mean Lateralisation Index of Alpha, Theta and Standard Error in the Y Axis and EEG Channel Pairs on the X Axis Where O Is Occipital, C Is Central and F Is Frontal. The Level of Significance Is Depicted as *p ≤ .05, *** p ≤ .001.
Changes in HRV between the EC supine and EC sitting positions are summarised in Table 5. The mean RR interval increased significantly in the supine position, indicating a slower HR. Both the mean HR and the minimum and maximum HRs were lower in the supine position (p < .001). LF power was significantly higher in the sitting position, while HF power was significantly higher in the supine position (p < .001).
Table 5. Heart Rate Variability Parameters in Supine and Sitting Position in EC Condition.
| HRV Parameters (Unit) | EC Supine | EC Sitting |
| Mean RR (sec) | 997.10 ± 74.54 | 837.88 ± 89.64*** |
| Mean HR | 60.50 ± 4.66 | 72.40 ± 7.68*** |
| Min HR | 55.90 ± 6.42 | 65.37 ± 7.28*** |
| Max HR | 71.04 ± 9.17 | 83.84 ± 9.88*** |
| LF power (n.u.) | 50.55 ± 12 | 63.10 ± 11.67*** |
| HF power (n.u.) | 49.35 ± 11.94 | 36.84 ± 11.63*** |
| LF/HF | 1.15 ± 0.55 | 2.16 ± 1.55** |
Note: Values are represented as mean ± SD; Level of significance is shown as **p ≤ .01; ***p ≤ .001. RR interval means time between two consecutive R waves; n.u. = normalized units.
Discussion
This study illustrated effects of different body postures on our body and brain relaxation when in resting in supine and sitting in EC condition. Using ML tools and statistical analysis on data from EEG and HRV, we gained valuable insights into how these postures influence our relaxation levels and physiological states.
In this pilot study, the used ML models, that is, RF, SVM, KNN and XGBoost, were effective in classifying relaxation states based on EEG signal. SVM performed best, with high accuracy and strong discriminative capabilities. The successful implementation of ML in this study highlights that by leveraging these advanced models, we can enhance our understanding and treatment of various brain-related conditions for broader applications in EEG analysis.
Significant increase in the absolute alpha power during supine position compared to sitting in EC condition suggests achievement of a deeper state of relaxation and less mental engagement, with a reduction in the visual and sensory processing. Similarly, significant increased theta power while in EC supine, indicated this state promotes profound relaxation akin to meditative states.
Observation of significant changes in alpha and theta relative power between the EC supine and EC sitting postures ensured achieving relaxation states without getting into sleep. 37 In the EC supine posture, consistent higher alpha power in the central, frontal and occipital regions is indicative of relaxation and reduced mental engagement suggests that the supine position promotes greater relaxation compared to sitting.30, 37 In the occipital region, increased alpha power reflects reduced visual processing demands, while in the central region, it suggests decreased somatosensory and motor processing. The frontal region showed reduced mental effort, aligning with increased calmness and relaxation. The consistent rise in alpha power across all EEG channels in the supine position highlights a general state of relaxation, with implications for activities requiring mental and physical rest, such as meditation.
Increased in the EC supine posture increased theta power, associated with relaxation, drowsiness and meditative states support the idea that lying down inhibits cortical activity, enhances relaxation and may benefit cognitive activities by promoting a more restful state even reported in other mental states.38–42 This study provided important insight into positional changes in the EEG in the EC states even though comparison of EC and EO in states provides role of visual stimulus only.31, 32, 42–46 The Yogic practices like Yoga Nidra are generally carried out in corpse position, but it can be performed in sitting position as well; similarly Zen and Vipassna practices can be performed in multiple positional states.47–50 This study provides broader framework to test ML tools to explore neural correlates of relaxation in various condition of practices. 51
In the occipital lobe channel, decreased alpha LI during EC supine condition suggested reduction in cognitive functions in comparison to EC sitting which may be consistent with attention processing demands even in EC state. The negative alpha LI values during both postures of EC sitting and EC supine indicated minimal hemispheric dominance, implying a balanced cognitive state. Similarly, reduced alpha LI in frontal lobe during supine position compared to sitting suggests left hemisphere dominance, often linked to emotional processing and cognitive engagement thereby reflecting increased relaxation. The theta LI values are near zero in occipital and frontal channels for both postures suggesting no significant hemispheric dominance, which aligns with a relaxed cognitive state.
In the central lobe, the negative LI values for alpha in both EC sitting and EC supine suggested a slight right hemisphere dominance, indicating consistent cognitive processing or attentional focus. The positive LI values for theta in both postures indicate balanced engagement between hemispheres, with a slight left hemisphere engagement during EC sitting and a more balanced state in EC supine. These patterns of increased alpha and theta power across both hemispheres could guide the development of relaxation techniques tailored to individual neural activity and hemispheric dominance.
The potential application of AI–ML tools is fast growing with availability of large digital data sets and thus opening new avenues and holds future for real-time monitoring systems for relaxation and stress management in healthy population as well as for therapeutic well-being assistance and also early detection of various neurodegenerative diseases including dementia, Alzheimer’s disease, depression, epilepsy, Parkinson’s disease, schizophrenia and even for forensic age mapping.52–62 These techniques can also be applied to other neuroimaging data derived from functional magnetic resonance imaging (fMRI) and positron emission tomography (PET) scans, offering more precise and personalised insights into brain activity. These findings suggest that brain states differ significantly between the two postures: EC sitting promotes more left hemisphere engagement linked to emotional processing and cognitive activity, while EC supine facilitates a more balanced or relaxed state, as indicated by the generally lower LI values across channels. Moreover, recent studies on role of alpha hemispheric power during various condition including normal sleep, aging and under condition of stimulus suggest for its broader implication in attention control that may not entirely depend on a particular task.63–65
Conclusion and Limitations
This pilot study emphasises the intricate connection between body posture, brain responses and relaxation levels. This research contributes to a better understanding of posture influences on our physical responses and cognitive processes, with potential implications for healthcare, neurology, and practices promoting wellness/Yoga programs.
One limitation of this study was small sample size and repeated data from the same participant due to limited time study for thesis work. Larger sample size from various age groups for generalisability, less bias, more channel (high density EEG for propagation study) would be appropriate. Beyond the models used in this study, other ML algorithms like decision trees, gradient boosting machines, naive Bayes and ensemble methods can be explored for EEG analysis. Each of these classifiers offers unique strengths and could contribute to more robust and accurate classification systems. Exploring these algorithms could further enhance the detection and monitoring of relaxation states and other cognitive conditions.
Acknowledgements
KKG thanks SCTIMST, Trivandrum, an Institute of National Importance under Department of Science and Technology (DST), Government of India for providing the infrastructure and facility for conducting this pilot study. KKG acknowledges the research grant DST/SATYAM/2020/303 dated 29/01/2024 from DST. This research study was carried out at SCTIMST, Trivandrum towards the MSc thesis work of CG (Student, Department of Computational Biology & Bioinformatics, University of Kerala, Thiruvananthapuram, India).
The authors declared no potential conflicts of interest with respect to the research, authorship and/or publication of this article.
Funding: The authors received following financial support for the research, authorship and/or publication of this article: The author (KKG) utilised learning resource allowance from her institute for publication of this article.
ORCID iD: Kamalesh K Gulia
https://orcid.org/0000-0002-2253-2644
Authors’ Contributions
KKG conceived the idea, recruitment of subject, conduction of study, interpretation of results, analysis and drafting of manuscript, overall supervision of the study and approved the final version of the manuscript.
CG helped in EEG analysis and drafting of manuscript and approved the final version of the manuscript.
Data Availability Statement
The datasets generated during and/or analysed during this study are available from the corresponding author on reasonable request.
Statement of Ethics
This study was approved by the Institutional Ethics Committee the Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum (SCT/IEC/2074/AUGUST/2023) and written informed consent was taken from the subject.
References
- 1.Adrian ED, and Yamagiwa K.. The origin of the Berger rhythm. Brain 1935; 58: 323–351. [Google Scholar]
- 2.Tudor M, Tudor L and Tudor KI.. Hans Berger (1873–1941) - The history of electroencephalography. Acta Med Croatica 2005; 59(4): 307–313. [PubMed] [Google Scholar]
- 3.Acharya RU, Faust O, Kannathal N, et al. Non-linear analysis of EEG signals at various sleep stages. Comput Methods Programs Biomed 2005; 80: 37–45. DOI: 10.1016/j.cmpb.2005.06.011 [DOI] [PubMed] [Google Scholar]
- 4.Llinás RR, and Steriade M.. Bursting of thalamic neurons and states of vigilance. J Neurophysiol 2006; 95: 3297–3308. DOI: 10.1152/jn.00166.2006 [DOI] [PubMed] [Google Scholar]
- 5.Knyazev GG. Cross-frequency coupling of brain oscillations: An impact of state anxiety. Int J Psychophysiol 2011; 80(3): 236–245. DOI: 10.1016/j.ijpsycho.2011.03.013 [DOI] [PubMed] [Google Scholar]
- 6.Gulia KK. Dynamism in activity of the neural networks in brain is the basis of sleep-wakefulness oscillations. Front Neurol 2012; 3: 38. DOI: 10.3389/fneur.2012.00038 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Nagendra RP, Maruthai and Kutty BM.. Meditation and its regulatory role on sleep. Front Neurol 2012; 3: 54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Aboalayon KAI, Faezipour M, Almuhammadi WS, et al. Sleep stage classification using EEG signal analysis: A comprehensive survey and new investigation. Entropy 2016; 18(9): 272. DOI: 10.3390/e18090272 [Google Scholar]
- 9.Nunez MD, Nunez PL, and Srinivasan R.. Electroencephalography (EEG): Neurophysics, experimental methods, and signal processing. In: Ombao H, Linquist M, Thompson W and Aston J (eds) Handbook of neuroimaging data analysis , 2016, pp. 175–197. DOI: 10.13140/rg.2.2.12706.63687 [Google Scholar]
- 10.Gemein LAW, Schirrmeister RT, Chrabąszcz P, et al. Machine-learning-based diagnostics of EEG pathology. Neuroimage 2020; 220: 117021. DOI: 10.1016/j.neuroimage.2020.117021 [DOI] [PubMed] [Google Scholar]
- 11.Frohlich J, Toker D and Monti MM.. Consciousness among delta waves: A paradox? Brain 2021; 144: 2257–2277. DOI: 10.1093/brain/awab095 [DOI] [PubMed] [Google Scholar]
- 12.Alexander R, Aragón OR, Bookwala J, et al. The neuroscience of positive emotions and affect: Implications for cultivating happiness and wellbeing. Neurosci Biobehav Rev 2021; 121: 220–249. DOI: 10.1016/j.neubiorev.2020.12.002 [DOI] [PubMed] [Google Scholar]
- 13.Chattu VK, Manzar MD, Kymary S, et al. The global problem of insufficient sleep and its serious public health implications. Healthcare (Basel) 2018; 7(1): 1. DOI: 10.3390/healthcare7010001 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Gulia KK, and Kumar VM.. Importance of sleep for health and wellbeing amidst COVID-19 pandemic. Sleep Vigil 2020; 4(1): 49–50. DOI: 10.1007/s41782-020-00087-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Gulia KK, and Kumar VM.. Sleep disorders in the elderly: A growing challenge. Psychogeriatrics 2018; 18(3): 155–165. DOI: 10.1111/psyg.12319 [DOI] [PubMed] [Google Scholar]
- 16.Radhakrishnan A, Aswathy BS, Kumar VM, et al. Sleep deprivation during late pregnancy produces hyperactivity and increased risk-taking behavior in offspring. Brain Res 2015; 1596: 88–98. DOI: 10.1016/j.brainres.2014.11.021 [DOI] [PubMed] [Google Scholar]
- 17.Jacobs GD, and Friedman R.. EEG spectral analysis of relaxation techniques. Appl Psychophysiol Biofeedback 2004; 29(4): 245–254. [DOI] [PubMed] [Google Scholar]
- 18.Barry RJ, Clarke AR, Johnstone SJ, et al. EEG differences between eyes-closed and eyes-open resting conditions. Clin Neurophysiol 2007; 118(12): 2765–2773. [DOI] [PubMed] [Google Scholar]
- 19.Sharma A and Singh M.. Assessing alpha activity in attention and relaxed state: An EEG analysis. In 2015 1st International Conference on Next Generation Computing Technologies (NGCT) 2015. Sep 4 (pp. 508–513). IEEE. [Google Scholar]
- 20.Kumar JS, and Bhuvaneswari P.. Analysis of electroencephalography (EEG) signals and its categorization–A study. Procedia Engineering 2012; 38: 2525–2536. [Google Scholar]
- 21.Harmony T. The functional significance of delta oscillations in cognitive processing. Front Integr Neurosci 2013; 7: 83. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Ikkai A, Dandekar S and Curtis CE.. Lateralization in alpha-band oscillations predicts the locus and spatial distribution of attention. PLoS One 2016; 11(5): e0154796. DOI: 10.1371/journal.pone.0154796 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Mumtaz W, Malik AS, Mohd MA, et al. Review on EEG and ERP predictive biomarkers for major depressive disorder. Biomed Signal Processing Control 2015; 22: 85–98. ISSN; 1746–8094. DOI: 10.1016/j.bspc.2015.07.003 [Google Scholar]
- 24.Bacigalupo F and Luck SJ.. Lateralized suppression of alpha-band EEG activity as a mechanism of target processing. J Neurosci 2019; 39(5): 900–917. DOI: 10.1523/JNEUROSCI.0183-18.2018 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Klatt LI, Getzmann S, Begau A, et al. A dual mechanism underlying retroactive shifts of auditory spatial attention: Dissociating target- and distractor-related modulations of alpha lateralization. Sci Rep 2020; 10: 13860. DOI: 10.1038/s41598-020-70004-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Alipoor M, Suratgar AA, and Pooyan M.. Classification of EEG signals in four groups, including healthy subjects with open/closed eyes and epilepsy subjects with/without seizure by PSD estimate (Using the Multitaper Method) and ANN. 5th International Symposium on Health Informatics and Bioinformatics 2010; 98–103. [Google Scholar]
- 27.Sinha N and Babu D.. Statistical feature analysis for EEG baseline classification: Eyes Open vs Eyes Closed. In 2016 IEEE region 10 conference (TENCON) 2016. Nov 22 (pp. 2466–2469). IEEE. [Google Scholar]
- 28.Saidatul A, Paulraj MP, Yaacob S, et al. Analysis of EEG signals during relaxation and mental stress condition using AR modeling techniques. In 2011 IEEE International Conference on Control System, Computing and Engineering 2011. Nov 25 (pp. 477–481). IEEE. [Google Scholar]
- 29.Laport F, Castro PM, Dapena A, et al. Study of machine learning techniques for EEG eye state detection. In Proceedings 2020. Aug 31 (Vol. 54, No. 1, p. 53). MDPI. [Google Scholar]
- 30.Mahato S and Paul S.. Classification of depression patients and normal subjects based on electroencephalogram (EEG) signal using alpha power and theta asymmetry. J Med Syst 2020; 44: 1–8. DOI: 10.1007/s10916-019-1486-z [DOI] [PubMed] [Google Scholar]
- 31.Mattiev J, Sajovik J, Drevensek G, et al. Assessment of model accuracy in eyes open and closed EEG data: Effect of data pre-processing and validation methods. Bioengineering (Basel) 2022; 10(1): 42. DOI: 10.3390/bioengineering10010042 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Kan DPX, Croarkin PE, Phang CK, et al. EEG differences between eyes-closed and eyes-open conditions at the resting stage for euthymic participants. Neurophysiology 2017; 49: 432–440. DOI: 10.1007/s11062-018-9706-6 [Google Scholar]
- 33.Krygier JR, Heathers JAJ, Shahrestani S, et al. Mindfulness meditation, well-being, and heart rate variability: A preliminary investigation into the impact of intensive Vipassana meditation. Int J Psychophysiol 2013; 89.3: 305–313, ISSN 0167-8760 [DOI] [PubMed] [Google Scholar]
- 34.Watanabe N, Reece J and Polus BI.. Effects of body position on autonomic regulation of cardiovascular function in young, healthy adults. Chiropr Osteopat 2007; 15: 19. DOI: 10.1186/1746-1340-15-19 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Kuo TBJ, Chen C, Hsu Y, et al. EEG beta power and heart rate variability describe the association between cortical and autonomic arousals across sleep. Auton Neurosci 2016; 194: 32–37. DOI: 10.1016/j.autneu.2015.12.001 [DOI] [PubMed] [Google Scholar]
- 36.Putilov AA, and Donskava OG.. Alpha attenuation soon after closing the eyes as an objective indicator of sleepiness. Clin Exp Pharmacol Physiol 2014; 41(12): 956–964. DOI: 10.1111/1440-1681.12311 [DOI] [PubMed] [Google Scholar]
- 37.Halgren M, Ulbert I, Bastuji H, et al. The generation and propagation of the human alpha rhythm. Edited by Gyorgy Buzsáki, New York University Neuroscience Institute, New York, NY, 116 (47): 23772–23782 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Spironelli C, Busenello J and Angrilli A.. Supine posture inhibits cortical activity: Evidence from Delta and Alpha EEG bands. Neuropsychologia 2016; 89: 125–131. ISSN 0028-3932 [DOI] [PubMed] [Google Scholar]
- 39.Dehnavi MS, Dehnavi VS, and Shafiee M.. Classification of mental states of human concentration based on EEG signal. 12th International Conference on Information and Knowledge Technology (IKT), Babol, Iran, Islamic Republic of , 2021, pp. 78–82. DOI: 10.1109/IKT54664.2021.9685731 [Google Scholar]
- 40.You SD. Classification of relaxation and concentration mental states with EEG. Information 2021; 12: 187. [Google Scholar]
- 41.Muehlhan M, Marxen M, Landsiedel J. et al. , The effect of body posture on cognitive performance: A question of sleep quality. Front Hum Neurosci 2014; 8: 171. DOI: 10.3389/fnhum.2014.00171 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Barry RJ, Clarke AR, Johnstone SJ, et al. EEG differences in children between eyes-closed and eyes open resting conditions. Clin Neurophysiol 2009; 120: 1806–1811. [DOI] [PubMed] [Google Scholar]
- 43.Fathillah MS, Jaafar R, Chellappan K, et al. A study on EEG signals during eye-closed and eye-open using discrete wavelet transform. 2016 IEEE EMBS Conference on Biomedical Engineering and Sciences (IECBES), Kuala Lumpur, Malaysia , 2016, pp. 674–678. DOI: 10.1109/IECBES.2016.7843535 [Google Scholar]
- 44.Gopan KG, and Sinha DJN.. Statistical feature analysis for EEG baseline classification: Eyes Open vs Eyes Closed. Published in IEEE Region 10 Conference 1 November 2016. DOI: 10.1109/TENCON.2016.7848476. Corpus ID: 12194720 [Google Scholar]
- 45.Nan W, Wan F, Tang Q, et al. Eyes-closed resting EEG predicts the learning of alpha down-regulation in neurofeedback training. Front Psychol . 2018; 9: 1607. DOI: 10.3389/fpsyg.2018.01607 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Li W, Xu Q, Li Y, et al. EEG characteristics in “eyes-open” versus “eyes-closed” condition during vibrotactile stimulation. Biomed Signal Processing Control 2021; 68: 102759. ISSN 1746–8094. DOI: 10.1016/j.bspc.2021.102759 [Google Scholar]
- 47.Gulia KK and Sreedharan SE.. Yoga Nidra, a non-pharmacological technique in management of insomnia and overall health in postmenopausal women. Sleep Med Clinics 2023; 18(4): 463–471. [DOI] [PubMed] [Google Scholar]
- 48.Gulia KK and Sreedharan SE.. Yogic sleep and walking protocol induced improvement in sleep and wellbeing in post-menopausal subject: A longitudinal case study during COVID lockdown. Sleep Vigilance 2022; 6(1): 229–233. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Kakumanu RJ, Nair AK, Venugopal R, et al. Dissociating meditation proficiency and experience dependent EEG changes during traditional Vipassana meditation practice. Biological Psychol 2018; 135: 65–75, ISSN 0301-0511. [DOI] [PubMed] [Google Scholar]
- 50.Cahn BR and Polich J.. Meditation (Vipassana) and the P3a event-related brain potential. Int J Psychophysiol 2009; 72(1): 51–60. DOI: 10.1016/j.ijpsycho.2008.03.013 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Zoubi OA, Stenfors CUD, and Cherkassky VL.. Machine learning of EEG spectra for classifying affective states: Vigorous walking and relaxation. Front Psychol 2018; 9: 1186.30042718 [Google Scholar]
- 52.Vivaldi F, Paone G and Sposato S.. EEG resting state microstates in individuals with high levels of perceived stress: A machine learning approach. Applied Sci 2021; 11(8): 3377. [Google Scholar]
- 53.Ahmad RF, Malik AS, Amin HU, et al. Classification of cognitive and resting states of the brain using EEG Features. IEEE International Symposium on Medical Measurements and Applications (MeMeA) 2016; 1–5. [Google Scholar]
- 54.Asha S, Sudalaimani C, Devanad P, et al. Resting state EEG microstate profiling and a machine-learning based classifier model in epilepsy. Cogn Neurodyn 2024; 18: 2419–2432. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Boytsova YA, and Danko SG.. EEG differences between resting states with eyes open and closed in darkness. Human Physiol 2010; 36: 367–369. [Google Scholar]
- 56.Espinoza AI, May P, Anjum MF, et al. A pilot study of machine learning of resting-state EEG and depression in Parkinson’s disease. Clin Park Relat Disord 2022; 7: 100166. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Jennings JL, Peraza LR, Baker M, et al. Investigating the power of eyes open resting state EEG for assisting in dementia diagnosis. Alzheimers Res Ther 2022; 14: 109. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Kaushik P, Yang H, Roy PP, et al. Comparing resting state and task-based EEG using machine learning to predict vulnerability to depression in a non-clinical population. Sci Reps 2023; 13(1): 7467. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Keihani A, Sajadi SS, Hasani M, et al. Bayesian optimization of machine learning classification of resting-state EEG microstates in schizophrenia: A proof-of-concept preliminary study based on secondary analysis. Brain Sci 2022; 12(11): 1497. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Khayretdinova M, Shovkun A, Degtyarev V, et al. Predicting age from resting-state scalp EEG signals with deep convolutional neural networks on TD-brain dataset. Front Aging Neurosci 2022; 14: 1367. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Lal U, Chikkankod AV and Longo L.. Fractal dimensions and machine learning for detection of Parkinson’s disease in resting-state electroencephalography. Neural Comput Appl 2024; 36: 8257–8280. [Google Scholar]
- 62.Mironov VI, Nazarchuk SV, and Demin EA.. Identification of human emotional states using EEG signal processing based on the LSTM neural network. IEEE 14th International Conference on Application of Information and Communication Technologies 2020; 1–4. [Google Scholar]
- 63.Liegel N, Schneider D, Wascher E, et al. Task prioritization modulates alpha, theta and beta EEG dynamics reflecting proactive cognitive control. Sci Rep 2022; 12(1): 15072. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Li Y and Zhang A.. Enhanced laterality index: A novel measure for hemispheric asymmetry. J Healthc Eng 2022; 8997108. DOI: 10.1155/2022/8997108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Zając-Lamparska L, Zabielska-Mendyk E, Zapała D, et al. Differences in the lateralization of theta and alpha power during n-back task performance between older and young adults in the context of the hemispheric asymmetry reduction in older adults (HAROLD) Model. Symmetry 2024; 16(12): 1623. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The datasets generated during and/or analysed during this study are available from the corresponding author on reasonable request.
