Next Article in Journal
Ecotoxicological Assessment of Soils Reclaimed with Waste
Previous Article in Journal
The Influence of Steel, Glass and Basalt Fibres on Selected Parameters of Construction Mortars
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

White Noise Exemplifies the Constrained Disorder Principle-Based Concept of Overcoming Malfunctions

1
Department of Otolaryngology-Head and Neck Surgery, Hadassah Medical Center, Faculty of Medicine, Hebrew University, P.O. Box 1200, Jerusalem 91120, Israel
2
Department of Medicine, Hadassah Medical Center, Faculty of Medicine, Hebrew University, P.O. Box 1200, Jerusalem 91120, Israel
*
Author to whom correspondence should be addressed.
Appl. Sci. 2025, 15(16), 8769; https://doi.org/10.3390/app15168769
Submission received: 30 June 2025 / Revised: 2 August 2025 / Accepted: 6 August 2025 / Published: 8 August 2025

Abstract

The Constrained Disorder Principle (CDP) characterizes systems by their inherent variability, which is regulated within dynamic boundaries to ensure optimal function and adaptability. In biological systems, this variability, or “noise”, is crucial for resilience and flexibility at various scales, ranging from genes and cells to more complex organ systems. Disruption of the boundaries that control this noise—whether through amplification or suppression—can lead to malfunctions and result in pathological conditions. White noise (WN), defined by equal intensity across all audible frequencies, is an exemplary clinical application of the CDP. It has been shown to stabilize disrupted processes and restore functional states by utilizing its stochastic properties within the auditory system. This paper explores WN-based therapies, specifically for the masking, habituation, and alleviation of tinnitus, a subjective perception of sound. It describes the potential to improve WN-based therapies’ effectiveness by applying the CDP and CDP-based second-generation artificial intelligence systems. Understanding the characteristics and limitations of these approaches is essential for their effective implementation across various fields.

1. Introduction

The Constrained Disorder Principle (CDP) defines systems based on their inherent noise, restricted by dynamic boundaries that influence the noise level. This framework allows for improved functionality in response to disturbances. The CDP suggests that noise can address malfunctions in complex systems [1].
White noise (WN) is a random signal that has equal intensity at all frequencies. It is a type of sound characterized by a uniform energy distribution across various frequency bands resulting from combining sounds at different frequencies [2]. WN is a fundamental concept in signal processing and statistical analysis. Due to its unique characteristics and behavior, white noise has various applications across various scientific fields [3].
This paper examines how WN-based therapy exemplifies the application of the CDP in clinical practice and supports the idea that order can emerge from disorder. It highlights the potential of utilizing WN to improve and correct disrupted systems, as well as the possibility of using CDP-based platforms to enhance effectiveness and overcome some of the challenges associated with the clinical use of WN.

1.1. The Constrained Disorder Principle Accounts for All Types of Noise in the Universe

The CDP describes systems according to their inherent noise, limited by dynamic boundaries that affect the noise level. It applies to all systems in the universe, characterizing them by their inherent variability. This variability is regulated by dynamic boundaries that continuously manage it, allowing for optimal adaptations to changes in both internal and external environments [1,4,5,6]. Per the CDP, all biological systems exhibit a certain noise level crucial for proper functioning. This noise affects genes, cellular activities, and entire organs [4,7,8,9,10,11,12,13,14,15,16,17,18,19,20].
According to the CDP, malfunctions in these systems arise from dysfunctions at their boundaries, leading to either excessive or insufficient variability needed for optimal efficiency. This understanding allows for the development of second-generation artificial intelligence (AI) systems capable of regulating the degree of noise in complex systems to address and prevent malfunctions [21].

1.2. White Noise Is a Random Signal with Equal Intensity Across Different Frequencies, Resulting in a Constant Power Spectral Density

White noise effectively demonstrates the CDP in the auditory system as a random signal. WN is a type of sound characterized by a uniform energy distribution across different frequency bands. It consists of all frequencies within the audible spectrum (20 Hz to 20,000 Hz) at equal intensity [22]. The spectral density of WN is flat, meaning its intensity remains constant across the human audible frequency range. Several vital characteristics define white Noise (WN): it has a continuous power spectral density across all frequencies, zero autocorrelation at any non-zero lag, and a flat frequency spectrum [23].
Additionally, it exhibits statistical independence between any two points in time. Its statistical features include a mean value typically zero, a probability distribution often Gaussian, and a constant and finite variance. When all the sounds a person can hear are combined, they create WN. Consequently, WN has unlimited bandwidth and a linear spectrum [24].
WN has several physical manifestations, including acoustic, electronic, and digital forms. Acoustic WN produces a consistent “shhhh” sound with equal energy across all frequency bands. Some tangible and straightforward examples of WN include the sounds of the sea crashing, rainfall, air conditioning units, fans, and static television [25,26]. Electronic WN refers to thermal noise found in resistors and shot noise produced by electronic devices. This noise results from the random movement of electrons. Digital WN consists of computer-generated random sequences, including pseudo-random number generators, commonly used in digital signal processing. WN exists within a spectrum of noise colors [27,28]. For example, Pink noise has decreasing intensity at higher frequencies; brown noise emphasizes lower frequencies, and blue noise shows increasing intensity at higher frequencies [29].
In discrete time, WN is a discrete signal made up of samples that create a sequence of serially uncorrelated random variables. Each of these variables has a mean of zero and a finite variance. A single instance of white noise can be regarded as a random shock. Furthermore, a random vector is classified as a WN vector or white random vector if each of its components has a probability distribution with a mean of zero, finite variance, and the components are statistically independent [30,31]. The joint probability distribution of a vector must equal the product of the individual distributions of its components. Sometimes, the samples need to be independent and have identical probability distributions. Independent and identically distributed random variables represent the simplest form of WN. The signal is referred to as additive white Gaussian noise if each sample follows a normal distribution with a mean of zero [32].
The samples of a white noise (WN) signal can be organized sequentially in time or along one or more spatial dimensions. In digital image processing, the pixels of a WN image are arranged in a rectangular grid. These pixels are independent random variables with a uniform probability distribution over a specified interval. Additionally, white noise can be applied to signals distributed over more complex domains, such as a sphere or a torus [33,34]. An infinite-bandwidth white noise signal is purely theoretical. The bandwidth of white noise is constrained by factors such as the noise generation mechanism, the transmission medium, and the limited capabilities of observation [35]. Therefore, signals are WN if they exhibit a flat spectrum across frequencies relevant to the specific context. Even a binary signal that can only take values of 1 or −1 can be considered WN if the sequence is statistically uncorrelated. Additionally, noise with a continuous distribution, like a normal distribution, can also be classified as white noise. The measure of WN is a generalization that applies to random elements in infinite-dimensional spaces, such as random fields [36,37].
To define the concept of WN in the context of continuous-time signals, it is essential to replace the notion of a random vector with that of a continuous-time random signal. A process is WN in the strongest sense if it consists of random variables that are statistically independent of their entire prior history [35,38]. In phylogenetically based statistical methods, WN can signify a lack of phylogenetic patterns in comparative data. In everyday contexts, it sometimes suggests “random conversation without substantial content” [39].
The characteristics of the WN demonstrate the CDP-based concept of “order from disorder” [7,8,9,10].

1.3. Platforms That Use the CDP to Leverage Noise to Correct Malfunctions

The CDP-based second-generation AI system is a platform that utilizes variability to address malfunctions [21]. Introducing variability into the stimulation regimens has been shown to enhance response to vagal stimulation for weight loss [40]. In patients with chronic diseases who experience a complete or partial loss of medication effectiveness, incorporating variability in dosing and timing—within predefined ranges—has effectively overcome this loss of response [1,6,21,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75].
The CDP-based platform functions through three main steps. The first step employs an open-loop system that introduces variability within predefined ranges. The second step utilizes a closed-loop system that personalizes and adjusts this variability to achieve optimal outcomes. Finally, the third step quantifies physiological variability signatures and integrates them into the algorithm, enhancing the system’s overall effectiveness [6,65,76,77].

1.4. Using White Noise to Treat Clinical Conditions

The CDP outlines a framework for using noise to correct system malfunctions [71,73,74]. Using WN to treat the disorder exemplifies the CDP-based concept of using noise. True WN is theoretically impossible to produce because of infinite bandwidth; however, practical implementations are limited by bandwidth [78]. The quality of WN depends on the effectiveness of the algorithm used. WN effectively masks unwanted sounds by adding either a natural or artificial sound to the environment. Research has also examined the changes in Mismatch Negativity (MMN) using WN masking. Notably, the amplitude of MMN is significantly reduced when subjected to contralateral WN masking [79,80]. WN can be generated digitally with a digital signal processor, microprocessor, or microcontroller. This process typically involves feeding a suitable stream of random numbers into a digital-to-analog converter. Different sources of WN are marketed as privacy enhancers, sleep aids, and tinnitus masks. Alternatively, tuning an AM radio to unused frequencies, often called “static”, is a more straightforward way to generate WN. Fans and air conditioners generate WN by producing countless audio frequencies, preventing the human brain from registering surrounding noises unless they are excessively loud [81,82,83].
WN has shown promise in treating various sleep-related conditions [3]. It has been found to improve sleep in environments with high levels of noise, based on both subjective reports and objective measurements from individuals having trouble sleeping due to such disturbances. WN improves sleep–wake cycles and decreases the time it takes to fall asleep. For patients with insomnia, it masks environmental disturbances, creates a consistent sound environment, and helps maintain sleep continuity. WN effectively reduces sleep latency in controlled environments, improves sleep quality metrics, and enhances overall sleep maintenance. WN decreases the difference between background and peak noise levels, raising the arousal threshold to noise [83,84,85]. WN leads to deeper sleep with fewer awakenings during the night. WN in the 50 to 75 dB range has positively affected participants’ sleep and wake cycles. When mixed-frequency WN was added to ambient noise, it significantly reduced sleep-induced arousal and disturbances, as the difference between background noise and peak sounds was considerably minimized [3,86,87]. It aligns with the CDP-based notion of the advantage of adding noise for overcoming challenges [4,5]. WN has also positively impacted sleep patterns in newborns, reducing crying in colicky babies and enhancing the sleep environment in neonatal intensive care units (NICUs). Infants exposed to WN have shown fewer nighttime awakenings and improved sleep quality. Children with autism spectrum disorder (ASD) reported fewer delays in sleep onset and a reduction in night waking after this intervention [88,89,90].
WN is effective in treating conditions such as depression, anxiety, stress, schizophrenia, and dementia, as well as in relieving pain [3,91,92,93]. It can help reduce stress responses and anxiety disorders by lowering cortisol levels and improving focus during anxiety-inducing situations. WN has also been beneficial in nursing homes, where it reduces verbal agitation in patients with dementia. Additionally, it decreased behavioral and psychological symptoms in patients with schizophrenia who also had dementia, and its improved symptoms of depression and anxiety. In elderly patients admitted to the intensive care units, WN contributed to a decreased heart rate, alleviated pain during vaccinations, and supported the development of sucking behaviors in newborns [94,95,96,97].
The impact of WN on cognitive function is mixed, which supports the CDP concept’s requirement for an appropriate range of noise under varying conditions. WN can enhance attention and concentration [98,99,100]. When played at volumes between 60 and 86 dB, white noise helps to reduce environmental distractions and improve attention, learning, and memory. The text enhances performance in tasks that involve sequential short-term memory. WN improves information processing in the nervous system, benefiting cognitive functions such as learning, memory, attention, and concentration. By engaging long-term memory structures like the hippocampus, WN effectively boosts learning capacity, making it easier to acquire new vocabulary [99,101,102,103].
WN can effectively address specific symptoms of attention deficit hyperactivity disorder (ADHD) [104]. Research has demonstrated that WN can enhance reading and writing speed, improve speech recognition, aid in managing behaviors outside of work, increase awareness, support working memory tasks, and sometimes improve task accuracy. For individuals with ADHD, WN can lead to better cognitive functioning by compensating for low basal dopamine levels that often occur due to dopamine transport disorders. However, WN may not have the same positive effects, or could even be counterproductive, for individuals with normal or high levels of attention. Background stimulation from WN enhances cognitive functioning in secondary students with ADHD while potentially decreasing performance among non-ADHD students [105,106,107,108].
WN can enhance work productivity. Implementing systems that mask ambient noise and improve concentration is essential to leverage the benefits of an open office layout while maintaining employee attention and focus [3,103,109]. WN-based systems that reduce distracting background noise are crucial in such environments. By minimizing noise fluctuations and creating a sense of privacy, WN decreases distractions, boosts employee moods, and improves performance, although it may hinder cognitive performance in complex card-sorting tasks. Additionally, WN offers several advantages, including enhanced learning abilities and improved memory retention, by optimizing the study environment. An experiment was conducted with sixty-six healthy participants to explore the benefits of using WN in a learning setting [103,110].
Using noise-reducing earplugs alongside rational and emotional treatment enhances the emotional and sleep states of colorectal cancer patients, yielding specific positive effects. This approach could serve as a potential nursing plan for these individuals [111]. Unperceivable electrical noise stimulation has improved postural control by enhancing somatosensory feedback. Pink and white noise signals alter the temporal behavior of the foot center of pressure (CoP) during quiet standing [112]. WN is commonly used in electronic music production, either directly or as an input for filters to generate noise signals. It plays a significant role in audio synthesis, particularly for replicating percussive instruments like cymbals and snare drums, which contain a considerable amount of high-frequency noise. WN also serves as the foundation for some random number generators [113,114].
These examples support the CDP-based concept of using noise within constraints to improve system functionality and overcome disturbances.

1.5. Using White Noise to Treat Tinnitus

Subjective tinnitus, defined as the perception of a sound without an external source, affects approximately 25% of the US population, with about 8% experiencing a chronic and debilitating condition [115,116]. It is associated with a nearly threefold increase in rates of depression and anxiety [117,118]. While factors such as noise exposure, sensorineural hearing loss, traumatic brain injury, concussion, drug exposure, and others are thought to contribute to tinnitus, most cases lack an identifiable cause [119]. Tinnitus arises primarily from the nervous system’s activity rather than mechanical or vibrational activity in the cochlea or external stimuli [120]. For individuals with mild hearing loss or the elderly, WN still affects their hearing. Since individuals with hearing loss often suffer from tinnitus, cognitive dysfunction, and depression, WN may provide a means of therapy for these patients [121,122,123].
Tinnitus is considered a brain disorder initiated by cochlear trauma, followed by neuronal hyperactivity in the cochlear nucleus and higher regions of the central auditory system, including the inferior colliculus, thalamus, and auditory cortex [124]. Neurons in these areas show increased activity in individuals with tinnitus, firing synchronously to compensate for cochlear hair cell damage [124]. There is no standardized treatment for tinnitus. Available options, including hearing aids, sound masking, drug therapies, acupuncture, and neuromodulation, have shown limited effectiveness. Cognitive-behavioral therapy has improved quality of life but does not significantly reduce tinnitus loudness [125,126,127].
Sound masking, employing broadband sound to alleviate tinnitus, was first described in the late 1970s [128]. WN provides sound masking, reduces the perceived intensity of tinnitus, and assists patients in habituating to the sounds associated with tinnitus [129,130]. This approach relieves stress with soothing sounds, diverts attention from tinnitus by increasing background noise, and alleviates the emotional burden of tinnitus [131]. Some individuals even report tinnitus suppression or temporary disappearance following masking therapy. However, evidence supporting its ability to suppress tinnitus remains limited [132,133]. A Cochrane review by Hobson et al. found no significant benefits of sound therapy alone. Still, the authors claimed that the “absence of conclusive evidence should not be interpreted as evidence of ineffectiveness” [132].
Early sound therapy approaches, known as “complete masking”, used devices resembling hearing aids to generate white noise at increased levels that completely obscured the tinnitus. Later, a different approach emerged, using the minimal appreciable level of white noise to promote habituation to the disordered auditory perception [132]. Another technique, “sound enrichment”, adjusts noise generators to produce sound at a level where the tinnitus and external noise blend. This method forms the basis of Tinnitus Retraining Therapy (TRT), which combines sound therapy with behavioral counseling [134]. Clinical trials comparing TRT with complete masking have shown that both methods significantly reduce tinnitus-related distress, with TRT yielding slightly more significant benefits [135,136]. Neuromonics Tinnitus Treatment (NTT) represents another method, combining noise with music to alleviate tinnitus. This six-month intervention requires patients to listen for at least two hours daily. During the initial two months, wideband noise is added to the music to mask tinnitus audibility during the quiet portions of the music. In the subsequent four months, the noise is removed, and patients gradually reduce the music volume to minimize the interaction between tinnitus and the music [137].
Patients often find that they respond better to external sounds that match the frequency of their tinnitus. Since white noise (WN) covers a broad range of frequencies, it can be particularly effective for treating various types of tinnitus because it can effectively mask different sounds at multiple frequencies. Using a tinnitus masker that continuously generates specific sound frequencies—often white noise—may be a successful treatment option for alleviating tinnitus symptoms. The intensity required to mask the tinnitus is typically lower when the masking noise is close to the frequency of the tinnitus itself. Patients with low-frequency tinnitus require higher intensity levels when using high-frequency narrowband noise and white noise, compared to those with high-frequency tinnitus. WN may facilitate the release of cognitive resources and reduce auditory effort under these conditions [132,138,139,140].
Other sound-based treatments, such as modulated sounds (low-rate amplitude tones within the tinnitus pitch range), pink noise (resembling natural sounds), speech noise, and high tones, have been shown to reduce patients’ complaints and even provide temporary tinnitus suppression [140,141,142].
Sound therapy is currently included as an optional treatment for managing tinnitus symptoms in clinical practice guidelines by the American Academy of Otolaryngology-Head and Neck Surgery [133]. These therapies are offered through devices worn in or behind the ear, often combined with hearing aids to enhance the patient’s hearing. They are also accessible via smartphone applications, gaming consoles, headphones, and audio devices [143].
Despite the lack of large randomized controlled trials confirming the efficacy of sound therapy for eliminating or significantly alleviating bothersome tinnitus, the existing literature highlights the rationale and variable success rates of different approaches. While sound therapy is generally considered safe with no reported side effects, it can be costly and requires prolonged use, often involving several hours of daily listening for months. Recent studies suggest that unstructured or random acoustic input can induce maladaptive neuroplastic changes in the central auditory system, even at levels below those considered harmful. Over time, this may undermine its structural and functional integrity, potentially worsening tinnitus [129].
Sensory input plays a crucial role in shaping neuronal organization and the development of sensory maps in the brain. Research has illuminated the mechanisms that regulate the plasticity of the auditory pathway, particularly by examining the effects of altered auditory input during critical developmental periods. During these times, plasticity optimizes neural circuits to better align with the external environment. Furthermore, studies conducted in adulthood indicate that hearing loss is often linked to the emergence of tinnitus [144,145]. The molecular, cellular, and circuit-level mechanisms that regulate neuronal organization and tonotopic map plasticity during both developmental critical periods and adulthood have been described. These mechanisms play a role in modulating disinhibitory networks, as well as in influencing synaptic structure and function, along with the structural barriers to plasticity [146]. The regulation of plasticity also involves neuromodulatory circuits that link plasticity to learning and attention. Both ascending and descending auditory circuits connect the auditory cortex to lower brain structures [147].

1.6. Potential Mechanisms Underlying the Positive Effects of WN

The CDP offers a platform that utilizes variability for the purpose of improvement [6,65,76,77,148]. It suggests bringing the system closer to its normal physiology by introducing noise where necessary. The exact mechanism behind WN’s benefits remains unclear, but they can be attributed to two well-known phenomena: stochastic resonance (SR) and noise masking [3,149,150,151].
Stochastic resonance (SR) is a well-established phenomenon in psychophysics that may explain the positive effects of white noise therapy [152]. Signal recovery (SR) occurs when a signal is too weak to be detected but can be amplified by adding noise. This random noise enhances neural communication through the phenomenon of SR, making the signal easier to detect. In the auditory nerve, many of the nerve fibers have a high spontaneous firing rate in silence, typically reaching up to 100 spikes per second. When there is a very small input of sound energy, the firing rate can increase to 105 spikes per second, indicating that the system is highly sensitive to minor changes. However, the actual signal-to-noise ratio is quite low, meaning that most of the detected signals are actually noise [153,154].
When unpredictable noise, such as WN, increases, it leads to a higher signal transmission and detection level, resulting in a better SNR [150,155]. The SR effect is influenced by both signal level and noise, following an inverted U-shaped curve where performance is highest at moderate noise levels [156,157,158]. Moderate levels of WN can enhance performance by providing enough power to elevate the signal above the detection threshold [150,159,160]. SR has several limitations, including the inverted U-curve dependency on noise levels [159]. This concept aligns with the CDP-based method of using noise to address malfunctions, and the noise needs to be constrained for optimal effects [6].
The CDP specifies various noise levels essential for optimal system performance, emphasizing the importance of dynamic noise boundaries to regulate noise levels and ensure effective adaptation to different environments [1,6,21,69,70,71,72]. Similarly, if there is too much WN, it can overpower the signal and hinder attention and performance [159].
It supports the CDP-based concept of a dynamic zone and suggests that an optimal level of variability is necessary for achieving peak performance. According to the CDP, the required degree of variability is influenced by both internal and external disruptions to systems [4,5,161].
SR attempts to clarify the paradox that the brain uses WN to differentiate between targeted stimuli and non-target noise. The central nervous system can distinguish the actual signal—representing the information being conveyed—from noise, which includes undefined neural inputs that can interfere with this signal. By modifying neural synchronization, specific brain regions responsible for certain functions can create transient networks that enhance perception, cognition, or action. Consequently, random noise can improve the detection of weak sensory signals, a phenomenon explained by SR [162,163,164].
WN masking is based on the idea that the brain tends to focus on recognizable patterns, such as speech, while filtering out indistinct sounds, like static noise [3,165,166]. Noise masking involves introducing low-level, random background white noise that corresponds to the frequencies of human speech, making it particularly useful in environments like workplaces. It is crucial to manage the volume and frequency of the added noise effectively. The noise should be loud enough to obscure conversations within a certain distance. Still, if it is too noisy, the brain may find it difficult to ignore, potentially disrupting other cognitive processes. When correctly managed, WN can mask speech without distracting or irritating the listener [79,100].
As outlined in the CDP, the necessity of managing noise levels emphasizes the significance of denoising methods in specific situations [1]. A new lightweight denoising technique for infrared images has been proposed, based on adversarial transfer learning. This method employs a generative adversarial network (GAN) framework and improves the model through a phased transfer learning strategy. It eliminates additive white Gaussian noise from infrared images, demonstrating exceptional denoising performance [167].

1.7. The CDP Addresses Some of the Current Challenges Associated with White Noise

There are several challenges associated with the use of WN. There is significant variability in how individuals respond to it, both within the same person and among different people. The effects of WN on cognitive functions are mixed, and there is a lack of validated treatment regimens. For maximum therapeutic benefit, it is recommended to use WN at a volume of 50–60 decibels—like the level of conversation—throughout the sleep period and at a distance of 1–2 m from the sound source. However, the long-term effects of continuous exposure and the optimal frequency distributions for specific conditions have yet to be defined [104,159,167,168,169].
According to the CDP, smart devices equipped with adaptive noise generation, which personalizes the degree and range of decibels of WN, can lead to better long-term outcomes [148,161,170,171,172,173]. By implementing a CDP-based algorithm that incorporates noise into treatment, adjusting the decibel range and treatment duration within predefined limits may enhance clinical effectiveness and address issues like incomplete response and loss of response seen in some patients [4,5,161].
The CDP-based AI system may regulate the treatment of WN at three levels [21]. The first level is an open-loop system that introduces randomization of the decibel range and treatment length within predefined limits. The second level is a closed-loop system that uses clinical response as an endpoint. It allows for dynamic personalization of decibel variability and treatment duration to achieve the desired outcome. The third level comprises variability markers, such as heart rate variability, neuronal noise, or sleep waves, which are quantified and integrated into treatment regimens. These variability signatures can also be biomarkers for predicting prognosis and selecting the most appropriate treatment plan [1,6,21,69,70,71,72]. The creation of variability-based diagnostic and treatment tools may improve their accuracy [68,72]. Figure 1 summarizes the use of WN based on the CDP concept and its potential applications.

2. Summary

WN has potential applications across multiple disciplines. Its mathematical properties and practical uses indicate its relevance in both theoretical research and practical applications. Understanding its characteristics and limitations is essential for effective implementation in various fields. Many of WN’s functionalities are based on the CDP and using CDP-based algorithms may enhance the effectiveness of this approach in clinical practice. Controlled trials are necessary to assess its effects on patients with tinnitus.

Author Contributions

Y.I. conceptualized, Y.I. and S.S.S. wrote the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors have no conflict of interest. Y.I. is the founder of Oberon Sciences.

Comment on References

The CDP is a new concept, and relevant references were included for clarity.

Abbreviations

CDPconstrained disorder principle
AIartificial intelligence
WNWhite noise
SRstochastic resonance

References

  1. Ilan, Y. The constrained disorder principle defines living organisms and provides a method for correcting disturbed biological systems. Comput. Struct. Biotechnol. J. 2022, 20, 6087–6096. [Google Scholar] [CrossRef] [PubMed]
  2. Barry, R.J.; De Blasio, F.M. Characterizing pink and white noise in the human electroencephalogram. J. Neural Eng. 2021, 18, 034001. [Google Scholar] [CrossRef]
  3. Ghasemi, S.; Fasih-Ramandi, F.; Monazzam, M.R.; Khodakarim, S. White Noise and Its Potential Applications in Occupational Health: A Review. Iran. J. Public Health 2023, 52, 488–499. [Google Scholar] [CrossRef]
  4. Ilan, Y. Making use of noise in biological systems. Prog. Biophys. Mol. Biol. 2023, 178, 83–90. [Google Scholar] [CrossRef] [PubMed]
  5. Ilan, Y. Constrained disorder principle-based variability is fundamental for biological processes: Beyond biological relativity and physiological regulatory networks. Prog. Biophys. Mol. Biol. 2023, 180, 37–48. [Google Scholar] [CrossRef]
  6. Sigawi, T.; Lehmann, H.; Hurvitz, N.; Ilan, Y. Constrained Disorder Principle-Based Second-Generation Algorithms Implement Quantified Variability Signatures to Improve the Function of Complex Systems. J. Bioinform. Syst. Biol. 2023, 6, 82–89. [Google Scholar] [CrossRef]
  7. Ilan, Y. Overcoming randomness does not rule out the importance of inherent randomness for functionality. J. Biosci. 2019, 44, 132. [Google Scholar] [CrossRef]
  8. Ilan, Y. Generating randomness: Making the most out of disordering a false order into a real one. J. Transl. Med. 2019, 17, 49. [Google Scholar] [CrossRef]
  9. Ilan, Y. Advanced Tailored Randomness: A Novel Approach for Improving the Efficacy of Biological Systems. J. Comput. Biol. 2020, 27, 20–29. [Google Scholar] [CrossRef] [PubMed]
  10. Ilan, Y. Order Through Disorder: The Characteristic Variability of Systems. Front. Cell Dev. Biol. 2020, 8, 186. [Google Scholar] [CrossRef]
  11. El-Haj, M.; Kanovitch, D.; Ilan, Y. Personalized inherent randomness of the immune system is manifested by an individualized response to immune triggers and immunomodulatory therapies: A novel platform for designing personalized immunotherapies. Immunol. Res. 2019, 67, 337–347. [Google Scholar] [CrossRef]
  12. Ilan, Y. Randomness in microtubule dynamics: An error that requires correction or an inherent plasticity required for normal cellular function? Cell Biol. Int. 2019, 43, 739–748. [Google Scholar] [CrossRef]
  13. Ilan, Y. Microtubules: From understanding their dynamics to using them as potential therapeutic targets. J. Cell. Physiol. 2019, 234, 7923–7937. [Google Scholar] [CrossRef]
  14. Ilan-Ber, T.; Ilan, Y. The role of microtubules in the immune system and as potential targets for gut-based immunotherapy. Mol. Immunol. 2019, 111, 73–82. [Google Scholar] [CrossRef]
  15. Forkosh, E.; Kenig, A.; Ilan, Y. Introducing variability in targeting the microtubules: Review of current mechanisms and future directions in colchicine therapy. Pharmacol. Res. Perspect. 2020, 8, e00616. [Google Scholar] [CrossRef]
  16. Ilan, Y. beta-Glycosphingolipids as Mediators of Both Inflammation and Immune Tolerance: A Manifestation of Randomness in Biological Systems. Front. Immunol. 2019, 10, 1143. [Google Scholar] [CrossRef] [PubMed]
  17. Ilan, Y. Microtubules as a potential platform for energy transfer in biological systems: A target for implementing individualized, dynamic variability patterns to improve organ function. Mol. Cell. Biochem. 2022, 478, 375–392. [Google Scholar] [CrossRef] [PubMed]
  18. Ilan, Y. Enhancing the plasticity, proper function and efficient use of energy of the Sun, genes and microtubules using variability. Clin. Transl. Discov. 2022, 2, e103. [Google Scholar] [CrossRef]
  19. Shabat, Y.; Lichtenstein, Y.; Ilan, Y. Short-Term Cohousing of Sick with Healthy or Treated Mice Alleviates the Inflammatory Response and Liver Damage. Inflammation 2021, 44, 518–525. [Google Scholar] [CrossRef] [PubMed]
  20. Rotnemer-Golinkin, D.; Ilan, Y. Personalized-Inherent Variability in a Time-Dependent Immune Response: A Look into the Fifth Dimension in Biology. Pharmacology 2022, 107, 417–422. [Google Scholar] [CrossRef]
  21. Ilan, Y. Second-Generation Digital Health Platforms: Placing the Patient at the Center and Focusing on Clinical Outcomes. Front. Digit. Health 2020, 2, 569178. [Google Scholar] [CrossRef]
  22. Nittono, H. High-frequency sound components of high-resolution audio are not detected in auditory sensory memory. Sci. Rep. 2020, 10, 21740. [Google Scholar] [CrossRef] [PubMed]
  23. Nagel, K.I.; McLendon, H.M.; Doupe, A.J. Differential influence of frequency, timing, and intensity cues in a complex acoustic categorization task. J. Neurophysiol. 2010, 104, 1426–1437. [Google Scholar] [CrossRef]
  24. Machens, C.K.; Stemmler, M.B.; Prinz, P.; Krahe, R.; Ronacher, B.; Herz, A.V. Representation of acoustic communication signals by insect auditory receptor neurons. J. Neurosci. 2001, 21, 3215–3227. [Google Scholar] [CrossRef] [PubMed]
  25. Reybrouck, M.; Podlipniak, P.; Welch, D. Music and Noise: Same or Different? What Our Body Tells Us. Front. Psychol. 2019, 10, 1153. [Google Scholar] [CrossRef]
  26. Pellegrino, G.; Pinardi, M.; Schuler, A.-L.; Kobayashi, E.; Masiero, S.; Marioni, G.; Di Lazzaro, V.; Keller, F.; Arcara, G.; Piccione, F.; et al. Stimulation with acoustic white noise enhances motor excitability and sensorimotor integration. Sci. Rep. 2022, 12, 1310. [Google Scholar] [CrossRef]
  27. Gupta, M. Thermal noise in nonlinear resistive devices and its circuit representation. Proc. IEEE 1982, 70, 788–804. [Google Scholar] [CrossRef]
  28. Mueller, H.; Weber, J.; Hornsby, B. The Effects of Digital Noise Reduction on the Acceptance of Background Noise. Trends Amplif. 2006, 10, 83–93. [Google Scholar] [CrossRef]
  29. Zhou, J.; Liu, D.; Li, X.; Ma, J.; Zhang, J.; Fang, J. Pink noise: Effect on complexity synchronization of brain activity and sleep consolidation. J. Theor. Biol. 2012, 306, 68–72. [Google Scholar] [CrossRef]
  30. Grauer, J. Random Noise Generation Using Fourier Series. J. Aircr. 2018, 55, 1754–1760. [Google Scholar] [CrossRef]
  31. Kuo, H.-H. White Noise Distribution Theory; Taylor & Francis Group: Oxford, UK, 2018. [Google Scholar]
  32. Iqbal, S.; Khan, T.M.; Naveed, K.; Naqvi, S.S.; Nawaz, S.J. Recent trends and advances in fundus image analysis: A review. Comput. Biol. Med. 2022, 151, 106277. [Google Scholar] [CrossRef] [PubMed]
  33. Chichilnisky, E.J. A simple white noise analysis of neuronal light responses. Network 2001, 12, 199–213. [Google Scholar] [CrossRef] [PubMed]
  34. Gardner, T.; Magnasco, M. Sparse Time-Frequency Representations. Proc. Natl. Acad. Sci. USA 2006, 103, 6094–6099. [Google Scholar] [CrossRef] [PubMed]
  35. Howard, R. White noise: A time domain basis. In Proceedings of the 2015 International Conference on Noise and Fluctuations (ICNF), Xi’an, China, 2–6 June 2015; pp. 1–4. [Google Scholar]
  36. Riechers, P.; Crutchfield, J. Fraudulent white noise: Flat power spectra belie arbitrarily complex processes. Phys. Rev. Res. 2021, 3, 013170. [Google Scholar] [CrossRef]
  37. Othman, H. Generalized free Gaussian white noise. Int. J. Adv. Math. Sci. 2016, 4, 18. [Google Scholar] [CrossRef]
  38. Van Etten, W.C. Introduction to Random Signals and Noise; John Wiley & Sons: Chichester, UK, 2006. [Google Scholar]
  39. Blomberg, S.P.; Garland, T., Jr.; Ives, A.R. Testing for phylogenetic signal in comparative data: Behavioral traits are more labile. Evolution 2003, 57, 717–745. [Google Scholar]
  40. Khoury, T.; Ilan, Y. Platform introducing individually tailored variability in nerve stimulations and dietary regimen to prevent weight regain following weight loss in patients with obesity. Obes. Res. Clin. Pract. 2021, 15, 114–123. [Google Scholar] [CrossRef]
  41. Kessler, A.; Weksler-Zangen, S.; Ilan, Y. Role of the Immune System and the Circadian Rhythm in the Pathogenesis of Chronic Pancreatitis: Establishing a Personalized Signature for Improving the Effect of Immunotherapies for Chronic Pancreatitis. Pancreas 2020, 49, 1024–1032. [Google Scholar] [CrossRef]
  42. Ishay, Y.; Kolben, Y.; Kessler, A.; Ilan, Y. Role of circadian rhythm and autonomic nervous system in liver function: A hypothetical basis for improving the management of hepatic encephalopathy. Am. J. Physiol. Gastrointest. Liver Physiol. 2021, 321, G400–G412. [Google Scholar] [CrossRef]
  43. Kolben, Y.; Weksler-Zangen, S.; Ilan, Y. Adropin as a potential mediator of the metabolic system-autonomic nervous system-chronobiology axis: Implementing a personalized signature-based platform for chronotherapy. Obes. Rev. 2021, 22, e13108. [Google Scholar] [CrossRef]
  44. Kenig, A.; Kolben, Y.; Asleh, R.; Amir, O.; Ilan, Y. Improving Diuretic Response in Heart Failure by Implementing a Patient-Tailored Variability and Chronotherapy-Guided Algorithm. Front. Cardiovasc. Med. 2021, 8, 695547. [Google Scholar] [CrossRef] [PubMed]
  45. Azmanov, H.; Ross, E.L.; Ilan, Y. Establishment of an Individualized Chronotherapy, Autonomic Nervous System, and Variability-Based Dynamic Platform for Overcoming the Loss of Response to Analgesics. Pain Physician 2021, 24, 243–252. [Google Scholar] [CrossRef]
  46. Potruch, A.; Khoury, S.T.; Ilan, Y. The role of chronobiology in drug-resistance epilepsy: The potential use of a variability and chronotherapy-based individualized platform for improving the response to anti-seizure drugs. Seizure 2020, 80, 201–211. [Google Scholar] [CrossRef]
  47. Isahy, Y.; Ilan, Y. Improving the long-term response to antidepressants by establishing an individualized platform based on variability and chronotherapy. Int. J. Clin. Pharmacol. Ther. 2021, 59, 768–774. [Google Scholar] [CrossRef] [PubMed]
  48. Khoury, T.; Ilan, Y. Introducing Patterns of Variability for Overcoming Compensatory Adaptation of the Immune System to Immunomodulatory Agents: A Novel Method for Improving Clinical Response to Anti-TNF Therapies. Front. Immunol. 2019, 10, 2726. [Google Scholar] [CrossRef]
  49. Kenig, A.; Ilan, Y. A Personalized Signature and Chronotherapy-Based Platform for Improving the Efficacy of Sepsis Treatment. Front. Physiol. 2019, 10, 1542. [Google Scholar] [CrossRef]
  50. Ilan, Y. Why targeting the microbiome is not so successful: Can randomness overcome the adaptation that occurs following gut manipulation? Clin. Exp. Gastroenterol. 2019, 12, 209–217. [Google Scholar] [CrossRef]
  51. Gelman, R.; Bayatra, A.; Kessler, A.; Schwartz, A.; Ilan, Y. Targeting SARS-CoV-2 receptors as a means for reducing infectivity and improving antiviral and immune response: An algorithm-based method for overcoming resistance to antiviral agents. Emerg. Microbes Infect. 2020, 9, 1397–1406. [Google Scholar] [CrossRef]
  52. Ishay, Y.; Potruch, A.; Schwartz, A.; Berg, M.; Jamil, K.; Agus, S.; Ilan, Y. A digital health platform for assisting the diagnosis and monitoring of COVID-19 progression: An adjuvant approach for augmenting the antiviral response and mitigating the immune-mediated target organ damage. Biomed. Pharmacother. 2021, 143, 112228. [Google Scholar] [CrossRef] [PubMed]
  53. Ilan, Y.; Spigelman, Z. Establishing patient-tailored variability-based paradigms for anti-cancer therapy: Using the inherent trajectories which underlie cancer for overcoming drug resistance. Cancer Treat. Res. Commun. 2020, 25, 100240. [Google Scholar] [CrossRef]
  54. Hurvitz, N.; Azmanov, H.; Kesler, A.; Ilan, Y. Establishing a second-generation artificial intelligence-based system for improving diagnosis, treatment, and monitoring of patients with rare diseases. Eur. J. Hum. Genet. 2021, 29, 1485–1490. [Google Scholar] [CrossRef] [PubMed]
  55. Ilan, Y. Digital Medical Cannabis as Market Differentiator: Second-Generation Artificial Intelligence Systems to Improve Response. Front. Med. 2021, 8, 788777. [Google Scholar] [CrossRef]
  56. Gelman, R.; Berg, M.; Ilan, Y. A Subject-Tailored Variability-Based Platform for Overcoming the Plateau Effect in Sports Training: A Narrative Review. Int. J. Environ. Res. Public Health 2022, 19, 1722. [Google Scholar] [CrossRef]
  57. Azmanov, H.; Bayatra, A.; Ilan, Y. Digital Analgesic Comprising a Second-Generation Digital Health System: Increasing Effectiveness by Optimizing the Dosing and Minimizing Side Effects. J. Pain Res. 2022, 15, 1051–1060. [Google Scholar] [CrossRef] [PubMed]
  58. Hurvitz, N.; Elkhateeb, N.; Sigawi, T.; Rinsky-Halivni, L.; Ilan, Y. Improving the effectiveness of anti-aging modalities by using the constrained disorder principle-based management algorithms. Front. Aging 2022, 3, 1044038. [Google Scholar] [CrossRef] [PubMed]
  59. Kolben, Y.; Azmanov, H.; Gelman, R.; Dror, D.; Ilan, Y. Using chronobiology-based second-generation artificial intelligence digital system for overcoming antimicrobial drug resistance in chronic infections. Ann. Med. 2023, 55, 311–318. [Google Scholar] [CrossRef]
  60. Lehmann, H.; Arkadir, D.; Ilan, Y. Methods for Improving Brain-Computer Interface: Using A Brain-Directed Adjuvant and A Second-Generation Artificial Intelligence System to Enhance Information Streaming and Effectiveness of Stimuli. Int. J. Appl. Biol. Pharm. Technol. 2023, 14, 42–52. [Google Scholar] [CrossRef]
  61. Adar, O.; Hollander, A.; Ilan, Y. The Constrained Disorder Principle Accounts for the Variability That Characterizes Breathing: A Method for Treating Chronic Respiratory Diseases and Improving Mechanical Ventilation. Adv. Respir. Med. 2023, 91, 350–367. [Google Scholar] [CrossRef]
  62. Ilan, Y. The Constrained Disorder Principle Accounts for The Structure and Function of Water as An Ultimate Biosensor and Bioreactor in Biological Systems. Int. J. Appl. Biol. Pharm. Technol. 2023, 14, 31–41. [Google Scholar] [CrossRef]
  63. Sigawi, T.; Hamtzany, O.; Shakargy, J.D.; Ilan, Y. The Constrained Disorder Principle May Account for Consciousness. Brain Sci. 2024, 14, 209. [Google Scholar] [CrossRef]
  64. Ilan, Y. Special Issue “Computer-Aided Drug Discovery and Treatment”. Int. J. Mol. Sci. 2024, 25, 2683. [Google Scholar] [CrossRef]
  65. Hurvitz, N.; Dinur, T.; Revel-Vilk, S.; Agus, S.; Berg, M.; Zimran, A.; Ilan, Y. A Feasibility Open-Labeled Clinical Trial Using a Second-Generation Artificial-Intelligence-Based Therapeutic Regimen in Patients with Gaucher Disease Treated with Enzyme Replacement Therapy. J. Clin. Med. 2024, 13, 3325. [Google Scholar] [CrossRef]
  66. Ilan, Y. Free Will as Defined by the Constrained Disorder Principle: A Restricted, Mandatory, Personalized, Regulated Process for Decision-Making. Integr. Psychol. Behav. Sci. 2024, 58, 1843–1875. [Google Scholar] [CrossRef]
  67. Ilan, Y. The Constrained Disorder Principle Defines Mitochondrial Variability and Provides A Platform for A Novel Mechanism for Improved Functionality of Complex Systems. Fortune J. Health Sci. 2024, 7, 338–347. [Google Scholar] [CrossRef]
  68. Sigawi, T.; Israeli, A.; Ilan, Y. Harnessing Variability Signatures and Biological Noise May Enhance Immunotherapies’ Efficacy and Act as Novel Biomarkers for Diagnosing and Monitoring Immune-Associated Disorders. Immunotargets Ther. 2024, 13, 525–539. [Google Scholar] [CrossRef] [PubMed]
  69. Ilan, Y. Improving Global Healthcare and Reducing Costs Using Second-Generation Artificial Intelligence-Based Digital Pills: A Market Disruptor. Int. J. Environ. Res. Public Health 2021, 18, 811. [Google Scholar] [CrossRef] [PubMed]
  70. Ilan, Y. Next-Generation Personalized Medicine: Implementation of Variability Patterns for Overcoming Drug Resistance in Chronic Diseases. J. Pers. Med. 2022, 12, 1303. [Google Scholar] [CrossRef]
  71. Hurvitz, N.; Ilan, Y. The Constrained-Disorder Principle Assists in Overcoming Significant Challenges in Digital Health: Moving from “Nice to Have” to Mandatory Systems. Clin. Pract. 2023, 13, 994–1014. [Google Scholar] [CrossRef]
  72. Sigawi, T.; Ilan, Y. Using Constrained-Disorder Principle-Based Systems to Improve the Performance of Digital Twins in Biological Systems. Biomimetics 2023, 8, 359. [Google Scholar] [CrossRef] [PubMed]
  73. Ilan, Y. Overcoming Compensatory Mechanisms toward Chronic Drug Administration to Ensure Long-Term, Sustainable Beneficial Effects. Mol. Ther. Methods Clin. Dev. 2020, 18, 335–344. [Google Scholar] [CrossRef]
  74. Bayatra, A.; Nasserat, R.; Ilan, Y. Overcoming Low Adherence to Chronic Medications by Improving their Effectiveness Using a Personalized Second-generation Digital System. Curr. Pharm. Biotechnol. 2024, 25, 2078–2088. [Google Scholar] [CrossRef]
  75. Hurvitz, N.; Lehman, H.; Hershkovitz, Y.; Kolben, Y.; Jamil, K.; Agus, S.; Berg, M.; Aamar, S.; Ilan, Y. A constrained disorder principle-based second-generation artificial intelligence digital medical cannabis system: A real-world data analysis. J. Public Health Res. 2025, 14, 22799036251337640. [Google Scholar] [CrossRef]
  76. Sigawi, T.; Gelman, R.; Maimon, O.; Yossef, A.; Hemed, N.; Agus, S.; Berg, M.; Ilan, Y.; Popovtzer, A. Improving the response to lenvatinib in partial responders using a Constrained-Disorder-Principle-based second-generation artificial intelligence-therapeutic regimen: A proof-of-concept open-labeled clinical trial. Front. Oncol. 2024, 14, 1426426. [Google Scholar] [CrossRef]
  77. Gelman, R.; Hurvitz, N.; Nesserat, R.; Kolben, Y.; Nachman, D.; Jamil, K.; Agus, S.; Asleh, R.; Amir, O.; Berg, M.; et al. A second-generation artificial intelligence-based therapeutic regimen improves diuretic resistance in heart failure: Results of a feasibility open-labeled clinical trial. Biomed. Pharmacother. 2023, 161, 114334. [Google Scholar] [CrossRef]
  78. Vargas-Drechsler, M.; Pallas-Areny, R. Thermal noise in a finite bandwidth. Instrum. Meas. Mag. IEEE 2002, 4, 23–25. [Google Scholar] [CrossRef]
  79. Pourfannan, H.; Mahzoon, H.; Yoshikawa, Y.; Ishiguro, H. Sound masking by a low-pitch speech-shaped noise improves a social robot’s talk in noisy environments. Front. Robot. AI 2024, 10, 1205209. [Google Scholar] [CrossRef] [PubMed]
  80. Lindín, M.; Correa, K.; Zurrón, M.; Díaz, F. Mismatch negativity (MMN) amplitude as a biomarker of sensory memory deficit in amnestic mild cognitive impairment. Front. Aging Neurosci. 2013, 5, 79. [Google Scholar] [CrossRef] [PubMed]
  81. Czaja, Z.; Kowalewski, M. A random signal generation method for microcontrollers with DACs. Metrol. Meas. Syst. 2018, 25, 675–687. [Google Scholar] [CrossRef]
  82. De Jong, R.W.; Davis, G.S.; Chelf, C.J.; Marinelli, J.P.; Erbele, I.D.; Bowe, S.N. Continuous white noise exposure during sleep and childhood development: A scoping review. Sleep Med. 2024, 119, 88–94. [Google Scholar] [CrossRef]
  83. Zhang, L. An Investigation of A White Noise-based App for Improving Sleep Quality. Acad. J. Sci. Technol. 2023, 7, 76–80. [Google Scholar] [CrossRef]
  84. Riedy, S.M.; Smith, M.G.; Rocha, S.; Basner, M. Noise as a sleep aid: A systematic review. Sleep Med. Rev. 2021, 55, 101385. [Google Scholar] [CrossRef]
  85. Ebben, M.R.; Yan, P.; Krieger, A.C. The effects of white noise on sleep and duration in individuals living in a high noise environment in New York City. Sleep Med. 2021, 83, 256–259. [Google Scholar] [CrossRef] [PubMed]
  86. Forquer, L.; Johnson, C. Continuous White Noise to Reduce Resistance Going to Sleep and Night Wakings in Toddlers. Child Fam. Behav. Ther. 2005, 27, 1–10. [Google Scholar] [CrossRef]
  87. Stanchina, M.; Abu-Hijleh, M.; Chaudhry, B.; Carlisle, C.; Millman, R. The influence of white noise on sleep in subjects exposed to ICU noise. Sleep Med. 2005, 6, 423–428. [Google Scholar] [CrossRef]
  88. Rodríguez-Montaño, V.M.; Puyana-Romero, V.; Hernández-Molina, R.; Beira-Jiménez, J.L. The Noise: A Silent Threat to the Recovery of Patients in Neonatal Intensive Care Units. Buildings 2024, 14, 2778. [Google Scholar] [CrossRef]
  89. Zhang, Q.; Huo, Q.; Chen, P.; Yao, W.; Ni, Z. Effects of white noise on preterm infants in the neonatal intensive care unit: A meta-analysis of randomised controlled trials. Nurs. Open 2024, 11, e2094. [Google Scholar] [CrossRef] [PubMed]
  90. Pietrzak, J.; Kurdyś-Bykowska, P.; Surówka, Ł.; Obuchowicz, A. Use of white noise-emitting devices in infants and small children as assessed by their parents. Paediatr. Fam. Med. 2019, 15, 291–296. [Google Scholar] [CrossRef]
  91. Zhu, L.; Zheng, L. Influence of White Sound on Sleep Quality, Anxiety, and Depression in Patients with Schizophrenia. Noise Health 2024, 26, 97–101. [Google Scholar] [CrossRef]
  92. Kaneko, Y.; Butler, J.; Saitoh, E.; Horie, T.; Fujii, M.; Sasaki, H. Efficacy of white noise therapy for dementia patients with schizophrenia. Geriatr. Gerontol. Int. 2013, 13, 808–810. [Google Scholar] [CrossRef]
  93. Ramaswamy, M.; Philip, J.L.; Priya, V.; Priyadarshini, S.; Ramasamy, M.; Jeevitha, G.C.; Mathkor, D.M.; Haque, S.; Dabaghzadeh, F.; Bhattacharya, P.; et al. Therapeutic use of music in neurological disorders: A concise narrative review. Heliyon 2024, 10, e35564. [Google Scholar] [CrossRef]
  94. Son, S.M.; Kwag, S.W. Effects of white noise in walking on walking time, state anxiety, and fear of falling among the elderly with mild dementia. Brain Behav. 2020, 10, e01874. [Google Scholar] [CrossRef]
  95. Ridder, H.; Stige, B.; Qvale, L.; Gold, C. Individual music therapy for agitation in dementia: An exploratory randomized controlled trial. Aging Ment. Health 2013, 17, 667–678. [Google Scholar] [CrossRef]
  96. Farokhnezhad Afshar, P.; Mahmoudi, A.; Abdi, A. The effect of white noise on the vital signs of elderly patients admitted to the cardiac care unit. J. Gerontol. 2016, 1, 27–34. [Google Scholar] [CrossRef]
  97. Akca, K.; Ozdemir, A.A. Effect of Soothing Noise on Sucking Success of Newborns. Breastfeed. Med. 2014, 9, 538–542. [Google Scholar] [CrossRef]
  98. Baum, N.; Chaddha, J. The Impact of Auditory White Noise on Cognitive Performance. J. Sci. Med. 2021, 3, 1–15. [Google Scholar] [CrossRef]
  99. Awada, M.; Becerik-Gerber, B.; Lucas, G.; Roll, S. Cognitive performance, creativity and stress levels of neurotypical young adults under different white noise levels. Sci. Rep. 2022, 12, 14566. [Google Scholar] [CrossRef] [PubMed]
  100. Jafari, M.J.; Khosrowabadi, R.; Khodakarim, S.; Mohammadian, F. The Effect of Noise Exposure on Cognitive Performance and Brain Activity Patterns. Open Access Maced. J. Med. Sci. 2019, 7, 2924–2931. [Google Scholar] [CrossRef]
  101. Sun, Z.; Hu, S.; Xie, S.; Wu, L.; Jiang, C.; Ding, S.; Zhang, Z.; Xu, W.; Li, H. Does background sound impact cognitive performance and relaxation states in enclosed office? Build. Environ. 2025, 267, 112313. [Google Scholar] [CrossRef]
  102. Rausch, V.; Bauch, E.; Bunzeck, N. White Noise Improves Learning by Modulating Activity in Dopaminergic Midbrain Regions and Right Superior Temporal Sulcus. J. Cogn. Neurosci. 2013, 26, 1469–1480. [Google Scholar] [CrossRef] [PubMed]
  103. Angwin, A.J.; Wilson, W.; Arnott, W.; Signorini, A.; Barry, R.; Copland, D. White noise enhances new-word learning in healthy adults. Sci. Rep. 2017, 7, 13045. [Google Scholar] [CrossRef] [PubMed]
  104. Nigg, J.T.; Bruton, A.; Kozlowski, M.B.; Johnstone, J.M.; Karalunas, S.L. Systematic Review and Meta-Analysis: Do White Noise and Pink Noise Help With Attention in Attention-Deficit/Hyperactivity Disorder? J. Am. Acad. Child Adolesc. Psychiatry 2024, 63, 778. [Google Scholar] [CrossRef]
  105. Pickens, T.; Khan, S.; Berlau, D. White Noise as a Possible Therapeutic Option for Children with ADHD. Complement. Ther. Med. 2018, 42, 151–155. [Google Scholar] [CrossRef]
  106. Lin, H.Y. The Effects of White Noise on Attentional Performance and On-Task Behaviors in Preschoolers with ADHD. Int. J. Environ. Res. Public Health 2022, 19, 15391. [Google Scholar] [CrossRef] [PubMed]
  107. Cook, A.; Johnson, C.; Bradley-Johnson, S. White Noise to Decrease Problem Behaviors in the Classroom for a Child With Attention Deficit Hyperactivity Disorder (ADHD). Child Fam. Behav. Ther. 2015, 37, 38–50. [Google Scholar] [CrossRef]
  108. Chen, I.-C.; Chan, H.-Y.; Lin, K.-C.; Huang, Y.-T.; Tsai, P.-L.; Huang, Y.-M. Listening to White Noise Improved Verbal Working Memory in Children with Attention-Deficit/Hyperactivity Disorder: A Pilot Study. Int. J. Environ. Res. Public Health 2022, 19, 7283. [Google Scholar] [CrossRef] [PubMed]
  109. Banbury, S.; Berry, D. Office noise and employee concentration: Identifying causes of disruption and potential improvements. Ergonomics 2005, 48, 25–37. [Google Scholar] [CrossRef]
  110. Soderlund, G.; Sikström, S.; Loftesnes, J.M.; Sonuga-Barke, E. The effects of background white noise on memory performance in inattentive school children. Behav. Brain Funct. 2010, 6, 55. [Google Scholar] [CrossRef] [PubMed]
  111. Wang, Y.; Fei, J.; Zheng, Y.; Li, P.; Ren, X.; An, Y. Effects of the Combination of Noise Reduction Earplugs with White Noise and Rational Emotional Therapy on Emotional States of Inpatients with Colorectal Cancer. Noise Health 2024, 26, 300–305. [Google Scholar] [CrossRef]
  112. Yamagata, M.; Kiyono, K.; Kimura, T. Long-range cross-correlations between center of pressure velocity and colored noises provided during quiet standing. Neurosci. Lett. 2024, 842, 138008. [Google Scholar] [CrossRef]
  113. Caetano, M.; Kafentzis, G.; Degottex, G.; Mouchtaris, A.; Stylianou, Y. Evaluating How Well Filtered White Noise Models the Residual from Sinusoidal Modeling of Musical Instrument Sounds. In Proceedings of the 2013 IEEE Workshop on Applications of Signal Processing to Audio and Acoustics, New Paltz, NY, USA, 20–23 October 2013. [Google Scholar]
  114. Arslan, S.; Yildirim, B. A Novel White Noise Generator as the Tracking Generator for Filter Measurements. AEU-Int. J. Electron. Commun. 2018, 96, 13–17. [Google Scholar] [CrossRef]
  115. Shargorodsky, J.; Curhan, G.C.; Farwell, W.R. Prevalence and characteristics of tinnitus among US adults. Am. J. Med. 2010, 123, 711–718. [Google Scholar] [CrossRef]
  116. Baguley, D.; McFerran, D.; Hall, D. Tinnitus. Lancet 2013, 382, 1600–1607. [Google Scholar] [CrossRef]
  117. Bhatt, J.M.; Lin, H.W.; Bhattacharyya, N. Prevalence, Severity, Exposures, and Treatment Patterns of Tinnitus in the United States. JAMA Otolaryngol. Head Neck Surg. 2016, 142, 959–965. [Google Scholar] [CrossRef] [PubMed]
  118. Maes, I.H.; Cima, R.F.; Vlaeyen, J.W.; Anteunis, L.J.; Joore, M.A. Tinnitus: A cost study. Ear Hear. 2013, 34, 508–514. [Google Scholar] [CrossRef]
  119. Lockwood, A.H.; Salvi, R.J.; Burkard, R.F. Tinnitus. N. Engl. J. Med. 2002, 347, 904–910. [Google Scholar] [CrossRef]
  120. Messina, A.; Corvaia, A.; Marino, C. Definition of Tinnitus. Audiol. Res. 2022, 12, 281–289. [Google Scholar] [CrossRef]
  121. Yuan, J.; Sun, Y.; Sang, S.; Pham, J.H.; Kong, W.-J. The risk of cognitive impairment associated with hearing function in older adults: A pooled analysis of data from eleven studies. Sci. Rep. 2018, 8, 2137. [Google Scholar] [CrossRef] [PubMed]
  122. Wu, X.; Wang, S.; Chen, S.; Wen, Y.-y.; Liu, B.; Xie, W.; Li, D.; Liu, L.; Huang, X.; Sun, Y.; et al. Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family. Neural Plast. 2018, 2018, 9425725. [Google Scholar] [CrossRef] [PubMed]
  123. Qiu, Y.; Chen, S.; Xie, L.; Xu, K.; Lin, Y.; Bai, X.; Zhang, H.-M.; Liu, X.-Z.; Jin, Y.; Sun, Y.; et al. Auditory Neuropathy Spectrum Disorder due to Two Novel Compound Heterozygous OTOF Mutations in Two Chinese Families. Neural Plast. 2019, 2019, 9765276. [Google Scholar] [CrossRef] [PubMed]
  124. Roberts, L.E.; Eggermont, J.J.; Caspary, D.M.; Shore, S.E.; Melcher, J.R.; Kaltenbach, J.A. Ringing ears: The neuroscience of tinnitus. J. Neurosci. 2010, 30, 14972–14979. [Google Scholar] [CrossRef]
  125. Hesser, H.; Weise, C.; Westin, V.Z.; Andersson, G. A systematic review and meta-analysis of randomized controlled trials of cognitive-behavioral therapy for tinnitus distress. Clin. Psychol. Rev. 2011, 31, 545–553. [Google Scholar] [CrossRef]
  126. Hoare, D.J.; Kowalkowski, V.L.; Kang, S.; Hall, D.A. Systematic review and meta-analyses of randomized controlled trials examining tinnitus management. Laryngoscope 2011, 121, 1555–1564. [Google Scholar] [CrossRef] [PubMed]
  127. Song, J.J.; Vanneste, S.; Van de Heyning, P.; De Ridder, D. Transcranial direct current stimulation in tinnitus patients: A systemic review and meta-analysis. Sci. World J. 2012, 2012, 427941. [Google Scholar] [CrossRef] [PubMed]
  128. Vernon, J. Attemps to relieve tinnitus. J. Am. Audiol. Soc. 1977, 2, 124–131. [Google Scholar]
  129. Attarha, M.; Bigelow, J.; Merzenich, M.M. Unintended Consequences of White Noise Therapy for Tinnitus-Otolaryngology’s Cobra Effect: A Review. JAMA Otolaryngol. Head Neck Surg. 2018, 144, 938–943. [Google Scholar] [CrossRef] [PubMed]
  130. Hoare, D.; Searchfield, G.; Refaie, A.; Henry, J. Sound Therapy for Tinnitus Management: Practicable Options. J. Am. Acad. Audiol. 2014, 25, 62–75. [Google Scholar] [CrossRef]
  131. Henry, J.A.; Zaugg, T.L.; Myers, P.J.; Schechter, M.A. Using therapeutic sound with progressive audiologic tinnitus management. Trends Amplif. 2008, 12, 188–209. [Google Scholar] [CrossRef]
  132. Hobson, J.; Chisholm, E.; El Refaie, A. Sound therapy (masking) in the management of tinnitus in adults. Cochrane Database Syst. Rev. 2012, 11, Cd006371. [Google Scholar] [CrossRef]
  133. Tunkel, D.E.; Bauer, C.A.; Sun, G.H.; Rosenfeld, R.M.; Chandrasekhar, S.S.; Cunningham, E.R., Jr.; Archer, S.M.; Blakley, B.W.; Carter, J.M.; Granieri, E.C.; et al. Clinical practice guideline: Tinnitus. Otolaryngol. Head Neck Surg. 2014, 151 (Suppl. 2), S1–S40. [Google Scholar] [CrossRef]
  134. Jastreboff, P.J.; Jastreboff, M.M. Tinnitus Retraining Therapy (TRT) as a method for treatment of tinnitus and hyperacusis patients. J. Am. Acad. Audiol. 2000, 11, 162–177. [Google Scholar] [CrossRef]
  135. Henry, J.A.; Schechter, M.A.; Zaugg, T.L.; Griest, S.; Jastreboff, P.J.; Vernon, J.A.; Kaelin, C.; Meikle, M.B.; Lyons, K.S.; Stewart, B.J. Outcomes of clinical trial: Tinnitus masking versus tinnitus retraining therapy. J. Am. Acad. Audiol. 2006, 17, 104–132. [Google Scholar] [CrossRef]
  136. Tyler, R.S.; Noble, W.; Coelho, C.B.; Ji, H. Tinnitus retraining therapy: Mixing point and total masking are equally effective. Ear Hear. 2012, 33, 588–594. [Google Scholar] [CrossRef]
  137. Davis, P.B.; Paki, B.; Hanley, P.J. Neuromonics Tinnitus Treatment: Third clinical trial. Ear Hear. 2007, 28, 242–259. [Google Scholar] [CrossRef]
  138. Oiticica, J.; Vasconcelos, L.G.E.; Horiuti, M.B. White noise effect on listening effort among patients with chronic tinnitus and normal hearing thresholds. Braz. J. Otorhinolaryngol. 2023, 90, 101340. [Google Scholar] [CrossRef]
  139. Wang, H.; Tang, D.; Wu, Y.; Zhou, L.; Sun, S. The state of the art of sound therapy for subjective tinnitus in adults. Ther. Adv. Chronic Dis. 2020, 11, 2040622320956426. [Google Scholar] [CrossRef]
  140. Mondelli, M.; Cabreira, A.F.; Matos, I.L.; Ferreira, M.C.; Rocha, A.V. Sound Generator: Analysis of the Effectiveness of Noise in the Habituation of Tinnitus. Int. Arch. Otorhinolaryngol. 2021, 25, e205–e212. [Google Scholar] [CrossRef] [PubMed]
  141. Lai, H.; Wang, G.; Zheng, Z.; Gao, M.; Li, S.; Wu, S. Pink noise: A potential sound therapy for tinnitus. Am. J. Transl. Res. 2023, 15, 6621–6625. [Google Scholar]
  142. Reavis, K.M.; Rothholtz, V.S.; Tang, Q.; Carroll, J.A.; Djalilian, H.; Zeng, F.G. Temporary suppression of tinnitus by modulated sounds. J. Assoc. Res. Otolaryngol. 2012, 13, 561–571. [Google Scholar] [CrossRef]
  143. Searchfield, G.D.; Sanders, P.J. A randomized single-blind controlled trial of a prototype digital polytherapeutic for tinnitus. Front. Neurol. 2022, 13, 958730. [Google Scholar] [CrossRef] [PubMed]
  144. Persic, D.; Thomas, M.E.; Pelekanos, V.; Ryugo, D.K.; Takesian, A.E.; Krumbholz, K.; Pyott, S.J. Regulation of auditory plasticity during critical periods and following hearing loss. Hear. Res. 2020, 397, 107976. [Google Scholar] [CrossRef] [PubMed]
  145. Chen, Z.; Yuan, W. Central plasticity and dysfunction elicited by aural deprivation in the critical period. Front. Neural Circuits 2015, 9, 26. [Google Scholar] [CrossRef]
  146. Ribic, A. Stability in the Face of Change: Lifelong Experience-Dependent Plasticity in the Sensory Cortex. Front. Cell. Neurosci. 2020, 14, 76. [Google Scholar] [CrossRef] [PubMed]
  147. Irvine, D.R.F. Plasticity in the auditory system. Hear. Res. 2018, 362, 61–73. [Google Scholar] [CrossRef] [PubMed]
  148. Ilan, Y. Using the Constrained Disorder Principle to Navigate Uncertainties in Biology and Medicine: Refining Fuzzy Algorithms. Biology 2024, 13, 830. [Google Scholar] [CrossRef] [PubMed]
  149. van der Groen, O.; Potok, W.; Wenderoth, N.; Edwards, G.; Mattingley, J.B.; Edwards, D. Using noise for the better: The effects of transcranial random noise stimulation on the brain and behavior. Neurosci. Biobehav. Rev. 2022, 138, 104702. [Google Scholar] [CrossRef]
  150. Othman, E.; Yusoff, A.N.; Mohamad, M.; Abdul Manan, H.; Giampietro, V.; Abd Hamid, A.I.; Dzulkifli, M.A.; Osman, S.S.; Wan Burhanuddin, W.I.D. Low intensity white noise improves performance in auditory working memory task: An fMRI study. Heliyon 2019, 5, e02444. [Google Scholar] [CrossRef]
  151. Yamagata, M.; Okada, S.; Tsujioka, Y.; Takayama, A.; Shiozawa, N.; Kimura, T. Effects of subthreshold electrical stimulation with white noise, pink noise, and chaotic signals on postural control during quiet standing. Gait Posture 2022, 94, 39–44. [Google Scholar] [CrossRef]
  152. Matthews, P.; Raul, P.; Ward, L.M.; van Boxtel, J.J.A. Stochastic resonance in the sensory systems and its applications in neural prosthetics. Clin. Neurophysiol. 2024, 165, 182–200. [Google Scholar] [CrossRef]
  153. Bender, D.A.; Ni, R.; Barbour, D.L. Spontaneous activity is correlated with coding density in primary auditory cortex. J. Neurophysiol. 2016, 116, 2789–2798. [Google Scholar] [CrossRef] [PubMed]
  154. Burkard, R. Hearing Disorders. In International Encyclopedia of Public Health; Heggenhougen, H.K., Ed.; Academic Press: Oxford, UK, 2008; pp. 273–281. [Google Scholar]
  155. Rufener, K.S.; Kauk, J.; Ruhnau, P.; Repplinger, S.; Heil, P.; Zaehle, T. Inconsistent effects of stochastic resonance on human auditory processing. Sci. Rep. 2020, 10, 6419. [Google Scholar] [CrossRef]
  156. Rousseau, D.; Chapeau-Blondeau, F. Suprathreshold stochastic resonance and signal-to-noise ratio improvement in arrays of comparators. Phys. Lett. A 2004, 321, 280–290. [Google Scholar] [CrossRef]
  157. Zhang, W.; Shi, P.; Li, M.; Han, D. A novel stochastic resonance model based on bistable stochastic pooling network and its application. Chaos Solitons Fractals 2021, 145, 110800. [Google Scholar] [CrossRef]
  158. Yu, H.; Galán, R.F.; Wang, J.; Cao, Y.; Liu, J. Stochastic resonance, coherence resonance, and spike timing reliability of Hodgkin–Huxley neurons with ion-channel noise. Phys. A Stat. Mech. Its Appl. 2017, 471, 263–275. [Google Scholar] [CrossRef]
  159. Helps, S.K.; Bamford, S.; Sonuga-Barke, E.J.; Söderlund, G.B. Different effects of adding white noise on cognitive performance of sub-, normal and super-attentive school children. PLoS ONE 2014, 9, e112768. [Google Scholar] [CrossRef]
  160. Zhou, H.; Molesworth, B.R.C.; Burgess, M.; Hatfield, J. The effect of moderate broadband noise on cognitive performance: A systematic review. Cogn. Technol. Work 2024, 26, 1–36. [Google Scholar] [CrossRef]
  161. Ilan, Y. The constrained-disorder principle defines the functions of systems in nature. Front. Netw. Physiol. 2024, 4, 1361915. [Google Scholar] [CrossRef]
  162. Schwarzkopf, D.S.; Silvanto, J.; Rees, G. Stochastic resonance effects reveal the neural mechanisms of transcranial magnetic stimulation. J. Neurosci. 2011, 31, 3143–3147. [Google Scholar] [CrossRef]
  163. Lefebvre, J.; Hutt, A.; Frohlich, F. Stochastic resonance mediates the state-dependent effect of periodic stimulation on cortical alpha oscillations. elife 2017, 6, e32054. [Google Scholar] [CrossRef]
  164. Vd Groen, O.; Tang, M.; Wenderoth, N.; Mattingley, J. Stochastic resonance enhances the rate of evidence accumulation during combined brain stimulation and perceptual decision-making. PLOS Comput. Biol. 2018, 14, e1006301. [Google Scholar] [CrossRef]
  165. Brocolini, L.; Parizet, E.; Chevret, P. Effect of masking noise on cognitive performance and annoyance in open plan offices. Appl. Acoust. 2016, 114, 44–55. [Google Scholar] [CrossRef]
  166. Cerisara, C.; Demange, S.; Haton, J.P. On noise masking for automatic missing data speech recognition: A survey and discussion. Comput. Speech Lang. 2007, 21, 443–457. [Google Scholar] [CrossRef]
  167. Guo, W.; Fan, Y.; Zhang, G. Lightweight Infrared Image Denoising Method Based on Adversarial Transfer Learning. Sensors 2024, 24, 6677. [Google Scholar] [CrossRef]
  168. Miller, M.; Donovan, C.-L.; Bennett, C.; Aminoff, E.; Mayer, R. Individual differences in cognitive style and strategy predict similarities in the patterns of brain activity between individuals. Neuroimage 2011, 59, 83–93. [Google Scholar] [CrossRef]
  169. Egeland, J.; Lund, O.; Kowalik-Gran, I.; Aarlien, A.; Söderlund, G. Effects of auditory white noise stimulation on sustained attention and response time variability. Front. Psychol. 2023, 14, 1301771. [Google Scholar] [CrossRef]
  170. Ilan, Y. The Constrained Disorder Principle Overcomes the Challenges of Methods for Assessing Uncertainty in Biological Systems. J. Pers. Med. 2025, 15, 10. [Google Scholar] [CrossRef]
  171. Ilan, Y. The constrained disorder principle and the law of increasing functional information: The elephant versus the Moeritherium. Comput. Struct. Biotechnol. Rep. 2025, 2, 100040. [Google Scholar] [CrossRef]
  172. Adar, O.; Shakargy, J.D.; Ilan, Y. The Constrained Disorder Principle: Beyond Biological Allostasis. Biology 2025, 14, 339. [Google Scholar] [CrossRef]
  173. Ilan, Y. The Relationship Between Biological Noise and Its Application: Understanding System Failures and Suggesting a Method to Enhance Functionality Based on the Constrained Disorder Principle. Biology 2025, 14, 349. [Google Scholar] [CrossRef]
Figure 1. The use of WN based on the CDP concept and its potential applications.
Figure 1. The use of WN based on the CDP concept and its potential applications.
Applsci 15 08769 g001
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Stern Shavit, S.; Ilan, Y. White Noise Exemplifies the Constrained Disorder Principle-Based Concept of Overcoming Malfunctions. Appl. Sci. 2025, 15, 8769. https://doi.org/10.3390/app15168769

AMA Style

Stern Shavit S, Ilan Y. White Noise Exemplifies the Constrained Disorder Principle-Based Concept of Overcoming Malfunctions. Applied Sciences. 2025; 15(16):8769. https://doi.org/10.3390/app15168769

Chicago/Turabian Style

Stern Shavit, Sagit, and Yaron Ilan. 2025. "White Noise Exemplifies the Constrained Disorder Principle-Based Concept of Overcoming Malfunctions" Applied Sciences 15, no. 16: 8769. https://doi.org/10.3390/app15168769

APA Style

Stern Shavit, S., & Ilan, Y. (2025). White Noise Exemplifies the Constrained Disorder Principle-Based Concept of Overcoming Malfunctions. Applied Sciences, 15(16), 8769. https://doi.org/10.3390/app15168769

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop