Will Bangura, M.S., CAB-ICB, CBCC-KA, CPDT-KA, FDM, FFCP
The Illusion of the Unfazed Dog: A Scientific Analysis of Shield K9’s High-Level E-Collar Demonstration
Table of Contents
A recent video featuring a trainer, Haz Othman, from Shield K9 Dog Training in Canada shows a working-line German Shepherd performing precision obedience under repeated high-intensity e-collar stimulation, reportedly having two electronic collars on one collar strap on the dog’s neck at level 127, the collar’s maximum output. The trainer presents this as proof that such tools are not aversive, claiming the dog is working “happily in drive.” To many viewers, including professional trainers, including Haz himself, and pet parents, the dog may appear calm, confident, and unbothered. Yet this appearance does not reflect the absence of electrical or physiological impact. Instead, it represents a complex interplay of neurobiological arousal, pain modulation, learning contingencies, and genetic resilience, factors that make the demonstration misleading when interpreted outside its scientific context.
This article examines, in detail, the underlying mechanisms that explain what is actually happening during such a demonstration. It dissects the neurophysiology of arousal and nociception, the effects of stress-induced analgesia, the behavioral conditioning processes in play, and the broader welfare implications documented in peer-reviewed research. The goal is not to condemn or sensationalize, but to provide a factual scientific framework so that professionals and pet parents can understand what they are seeing, and what they are not.
Shield K9 Dog Training Video
Haz Othman
(Confused About How E-Collars Work)
Neurophysiology of Nociception and Arousal
Electrical collars deliver current that depolarizes sensory and motor neurons through the skin and superficial musculature. Even at lower levels, e-collar pulses activate A-delta and C-fiber nociceptors, which are the same pathways that transmit pain and thermal sensations. The nervous system interprets this as discomfort or pain, depending on intensity, frequency, and duration.
At maximum output (level 127 on some collars), the current is strong enough to activate both nociceptive and motor pathways, producing brief muscle contractions and sharp sensory input. The absence of overt distress in the dog’s behavior does not indicate that nociceptive signaling is absent; it reflects neural modulation, not a neutral experience.
When a dog is highly aroused in prey or defense drive, its sympathetic nervous system (SNS) floods the body with catecholamines (adrenaline and norepinephrine). This activates the fight-or-flight response, increasing oxygenation, cardiac output, and glucose metabolism. Simultaneously, the periaqueductal gray (PAG) region of the midbrain triggers the release of endogenous opioids such as β-endorphins and enkephalins. These bind to μ-opioid receptors in the spinal cord and brainstem, inhibiting ascending pain signals (Butler & Finn, 2009). The phenomenon, known as stress-induced analgesia, allows animals and humans to perform under conditions that would otherwise be painful or disabling.
Thus, the dog in the Shield K9 video may indeed continue working in drive, focused and outwardly stable, because its neurochemical state is temporarily blunting pain perception. However, that does not mean no physiological stress occurs. Catecholamine and cortisol surges still engage the hypothalamic-pituitary-adrenal (HPA) axis, influencing heart rate, respiration, and thermoregulation long after the session ends.
Motor Drive, Dopaminergic Systems, and the Masking of Aversives
Performance under pressure is also shaped by motivational systems in the brain. According to Gray and McNaughton’s (2000) Reinforcement Sensitivity Theory, the Behavioral Activation System (BAS), driven by dopamine, motivates approach behaviors toward potential rewards, while the Behavioral Inhibition System (BIS) and Fight–Flight–Freeze System (FFFS) control avoidance and defensive responses. High-drive working dogs exhibit a predominance of BAS activation: their reward-seeking circuits, fueled by dopamine release in the nucleus accumbens, overpower avoidance tendencies.
This means that even when the dog experiences strong electrical stimulation, the expectation of access to a ball, decoy, or bite sleeve triggers dopamine-driven pursuit that masks competing avoidance motivations. The dog appears “happy,” but this behavioral output reflects competing neurochemical signals, not an absence of aversive input.
Neuroscientifically, the dog’s outward focus and precision performance are products of simultaneous approach motivation and pain modulation. This dual activation allows for controlled, goal-oriented behavior even under intense stimulation, a trait selectively reinforced over generations in protection-bred dogs.
Physiological Markers: Panting, Vocalization, and Thermoregulation
The heavy panting and intermittent vocalization often observed in such demonstrations are physiological clues of sympathetic arousal. Panting serves both as a thermoregulatory mechanism and as a byproduct of elevated metabolic rate during catecholamine release. When muscles contract repeatedly due to electrical stimulation and adrenaline drives increased metabolism, body temperature rises, necessitating rapid respiration for heat dissipation.
Vocalization can result from two overlapping sources: (1) reflexive responses to electrical activation of motor neurons controlling the larynx, and (2) affective vocalizations associated with arousal or frustration. The distinction is subtle and requires temporal analysis relative to the stimulus. Short, sharp yelps immediately following stimulation likely reflect a direct nociceptive reaction, whereas sustained barking or growling aligns with motivational arousal. Both can coexist in a single session.
Beerda et al. (1998) demonstrated that exposure to aversive stimuli increases cortisol, heart rate, and salivary changes consistent with stress activation, even when behavioral indicators appear mild. Therefore, physiological arousal markers alone cannot be taken as proof of comfort or distress; they are evidence of activation, not emotion.
Operant Mechanisms: Negative Reinforcement and Escape Learning
The trainer in the Shield K9 video repeatedly asserts that the dog is neither in pain nor afraid, even while being stimulated at the collar’s highest level. This assertion conflicts directly with the basic principles of operant conditioning and with the stated design of electronic collars themselves. Manufacturers of these devices explicitly acknowledge that the stimulus they deliver is an aversive stimulus, meaning it is intended to motivate behavioral change through discomfort.
If the collar were not producing discomfort, it could not function as either negative reinforcement or positive punishment, the two operant mechanisms upon which e-collar training relies. In negative reinforcement, a dog performs a behavior to escape or avoid discomfort. In positive punishment, a dog reduces or stops a behavior to avoid or terminate pain. If neither avoidance nor escape is occurring, if the dog feels nothing aversive—then no learning mechanism is operating. The tool would be functionally inert.
This logical contradiction exposes a central inconsistency in the trainer’s claim. Either the shock is sufficiently aversive to influence behavior, in which case discomfort is present, or it is neutral, in which case it cannot produce the claimed results. Behavioral science allows no third option. As Skinner (1938, 1953) established, reinforcement and punishment depend entirely on the consequences’ capacity to alter behavior. To deny that capacity while claiming efficacy is to reject the very framework that makes the tool meaningful.
The behavioral mechanism underlying this form of training is negative reinforcement. The shock is applied until the dog performs the desired behavior, at which point the stimulation stops. The cessation of the aversive strengthens the preceding behavior, a form of escape learning. This can produce precise, immediate responses, particularly in dogs conditioned through consistent pressure-release contingencies.
However, this is distinct from positive reinforcement, which strengthens behavior through the addition of a desired consequence (e.g., a toy or food). While both can yield compliance, their emotional and motivational correlates differ markedly. Negative reinforcement produces behavior maintained by the avoidance of discomfort, whereas positive reinforcement produces behavior maintained by the anticipation of reward. Neurobiologically, the former engages stress and fear circuits, the latter engages reward and learning circuits.
Over repeated sessions, dogs conditioned under high negative reinforcement thresholds may display what is termed behavioral suppression, a narrowing of behavioral repertoire to avoid error. While this can appear as precision, it also reduces spontaneity and exploratory behavior (Estes & Skinner, 1941). When repeatedly reinforced under these contingencies, such dogs often exhibit performance that appears almost robotic, animated, and intense, yet characterized by rigid, highly controlled movement patterns driven by escape motivation rather than voluntary initiative. The dog may seem full of energy and enthusiasm, but much of that animation reflects sympathetic arousal and the drive to terminate stimulation rather than relaxed, goal-directed choice. This phenomenon is well-documented in animal learning literature and has parallels in anxiety conditioning models (Maier & Seligman, 1976). behavioral suppression, a narrowing of behavioral repertoire to avoid error. While this can appear as precision, it also reduces spontaneity and exploratory behavior (Estes & Skinner, 1941). This phenomenon is well-documented in animal learning literature and has parallels in anxiety conditioning models (Maier & Seligman, 1976).
Scientific Evaluation of E-Collar Efficacy and Welfare
Controlled studies provide the necessary empirical lens to evaluate what is observable in demonstrations like Shield K9’s.
Efficacy: Cooper et al. (2014) conducted a randomized controlled trial on pet dogs with recall problems. The study found no significant performance difference between dogs trained with e-collars and those trained without, and reward-based dogs exhibited less stress behavior and more consistent recall success. The study’s design, with random allocation and blinded assessment, provides the most robust evidence available on the topic.
Welfare: Vieira de Castro et al. (2020) evaluated dogs in reward-based, mixed, and aversive-heavy schools using behavioral, physiological, and cognitive measures. Dogs from aversive-heavy schools showed more stress behaviors, higher cortisol, and pessimistic cognitive bias. These outcomes indicate that frequent aversive use correlates with a negatively valenced emotional state, even outside training sessions.
Complementary evidence: Schilder and van der Borg (2004) observed that dogs trained with shock collars exhibited residual stress behaviors in later sessions and even when the collar was not active, suggesting associative learning between context and aversive expectation.
These data do not claim that every shock-collar-trained dog is outwardly distressed; they demonstrate that aversive methods engage physiological stress systems and that reward-based approaches can achieve the same or better performance without such activation.
Genetic Resilience and Contextual Misinterpretation
The dog in the Shield K9 video is an extreme example of selection for drive and pressure tolerance. Working-line German Shepherds used in IGP and protection sports are bred for strong prey motivation, environmental stability, and rapid recovery from stress. Their neuroendocrine thresholds differ significantly from those of pet dogs. They exhibit enhanced dopaminergic drive circuitry, faster autonomic recovery, and reduced behavioral inhibition thresholds.
When such a dog continues to perform under high-intensity stimulation, it reflects a unique physiological profile, not a universal canine norm. Applying identical pressure to an average family dog would almost certainly evoke fear, avoidance, or defensive aggression. Thus, interpreting this video as evidence that “dogs are not bothered by high-level e-collars” is a fundamental category error: it extrapolates from a biological specialist to a population generalist.
Cognitive and Emotional Interpretation
It is also essential to distinguish between drive activation and positive affect. A dog working in prey drive under high stimulation is not necessarily “happy” in the emotional sense. Dopaminergic arousal can coexist with sympathetic stress activation; an animal can be highly motivated and physiologically stressed simultaneously. In neurobehavioral terms, motivation and welfare are not identical constructs.
High drive produces intense focus and energy, but it does not negate nociception. The dog’s tail position, muscle tension, and respiration in the video indicate elevated arousal consistent with stress-activation physiology. This does not prove suffering, but it confirms that the experience is not neutral.
The Broader Implication: Misleading Optics
When such demonstrations are presented publicly without context, they risk reinforcing misconceptions about e-collar safety and necessity. The optics, a powerful, confident dog appearing unbothered, suggest mastery and efficacy. Yet the underlying physiology tells a different story. The display conflates arousal with welfare and compliance with understanding.
For professionals, the scientific takeaway is that demonstrations of extreme pressure tolerance represent outliers rather than exemplars. For pet parents, the caution is clear: what a purpose-bred competition dog can endure in a controlled environment cannot be generalized to the family dog sleeping on your couch.
The Take Away
The Shield K9 video does not reveal a painless or benign process; it reveals a complex neurobehavioral interplay of pain modulation, dopaminergic drive, and learned escape behavior. The dog’s apparent composure is a product of neurochemical masking and selective breeding, not proof of harmlessness. Peer-reviewed research consistently shows that aversive training methods confer no performance advantage and pose quantifiable risks to welfare physiology.
Understanding these mechanisms matters. It empowers trainers to interpret behavior through the lens of science rather than spectacle, and it helps pet parents recognize that force-free, reinforcement-based methods are not sentimental alternatives; they are the empirically validated standard of humane and effective training.
Glossary of Terms
A-delta and C-fiber nociceptors – Specialized nerve fibers that transmit pain and temperature signals from the skin to the spinal cord and brain.
Aversive stimulus – Any event or sensation that an animal seeks to avoid or escape, such as a shock, loud sound, or spray. Used in training to decrease behavior.
Behavioral Activation System (BAS) – A brain system that drives approach behavior and motivation toward rewards. High BAS activation makes dogs eager and persistent.
Behavioral Inhibition System (BIS) – A brain system that slows or stops behavior when a dog anticipates punishment or conflict. It regulates caution and fear responses.
Behavioral suppression – A reduction in normal, spontaneous behaviors due to fear or stress. Dogs under strong suppression may appear precise or robotic but less flexible.
Catecholamines – Stress hormones such as adrenaline and norepinephrine released during arousal or excitement that increase heart rate and alertness.
Cognitive bias test – A scientific tool used to measure whether an animal’s emotional state is optimistic or pessimistic based on how it interprets ambiguous cues.
Conditioned compliance – When a dog obeys commands automatically due to learned pressure-release or punishment histories, not voluntary cooperation.
Dopamine – A neurotransmitter that produces pleasure, motivation, and drive, often released during reward anticipation or excitement.
Endogenous opioids – Natural chemicals such as endorphins produced by the brain that reduce pain perception under stress or excitement.
Escape learning / Negative reinforcement – A process where the dog performs a behavior to stop or avoid something unpleasant, like pressure or shock.
Fight–Flight–Freeze System (FFFS) – The brain system responsible for immediate defensive reactions to threats.
Hypothalamic–pituitary–adrenal (HPA) axis – The body’s stress-response network that controls cortisol release and physiological arousal.
Motivation vs. Welfare – Motivation describes drive or desire to perform a behavior. Welfare describes how the animal feels physically and emotionally. A dog can be motivated but still stressed.
Nociception – The detection of painful or harmful stimuli by the nervous system.
Operant conditioning – The process of learning where behavior is shaped by consequences, such as rewards or punishments (Skinner, 1938, 1953).
Periaqueductal gray (PAG) – A midbrain region that releases pain-suppressing chemicals during stress or threat.
Positive punishment – Adding an unpleasant stimulus (like a shock) to reduce or stop a behavior.
Positive reinforcement – Adding a pleasant stimulus (like a treat or toy) to increase a behavior.
Prey drive / Defense drive – Natural motivational systems that push dogs to chase or protect; strong in working-line dogs.
Reinforcement Sensitivity Theory – A theory of motivation (Gray & McNaughton, 2000) describing how the brain’s approach and avoidance systems control behavior.
Stress-induced analgesia – Temporary reduction of pain sensitivity caused by adrenaline and endorphin release during stress or excitement.
Sympathetic nervous system (SNS) – The part of the nervous system that activates during stress or excitement, preparing the body for action.
Working-line dog – A dog bred for high performance and resilience in police, military, or sport work, often with stronger drives and stress tolerance than companion dogs.
About the Author
Will Bangura, M.S., CAB-ICB, CBCC-KA, CPDT-KA, FFCP, is an internationally accredited Certified Canine Behaviorist with over five decades of experience in dog training and behavior, including 35 years as a full-time professional. His early foundation in the field began with compulsion-based training under the Koehler method, and he actively competed in American Kennel Club (AKC) obedience trials. Over time, his approach evolved—from traditional methods to balanced training, and ultimately to fully embracing humane, force-free, and positive reinforcement-based methodologies.
Driven by a commitment to scientific rigor and ethical practice, Will pursued advanced academic study in behavioral psychology, earning a Master of Science degree. He also completed postgraduate coursework in canine cognition through Harvard University, further deepening his understanding of animal behavior from a cognitive and affective science perspective.
Will has authored over 100 articles on dog training and canine behavior, contributing to both professional and public discourse on evidence-based, humane training methods. In addition to his extensive article contributions, he is the author of two books on dog behavior and training, which serve as foundational resources for both pet parents and behavior professionals.
He remains steadfast in his dedication to professional development, completing more than 100 hours of continuing education annually. His practice is grounded in the most current, science-backed approaches, prioritizing the emotional welfare, autonomy, and well-being of the dog above all.
His professional credentials include accreditation as a Certified Canine Behaviorist (CAB-ICB) through International Canine Behaviorists (ICB), certification as a Certified Behavior Consultant Canine (CBCC-KA), and Certified Professional Dog Trainer (CPDT-KA) through the Certification Council for Professional Dog Trainers (CCPDT). He is also a Fear-Free Certified Professional (FFCP), affirming his commitment to low-stress, emotionally supportive care and training.
Will provides professional dog behavior consulting and dog training in Phoenix Az, as well as virtual dog behavior consultations globally. Will specializes in severe dog aggression, reactivity, dog anxiety, separation-anxiety, dog anxiety, fears, phobias, and obsessive compulsive behaviors in dogs.
References
Beerda, B., Schilder, M. B. H., van Hooff, J. A. R. A. M., de Vries, H. W., & Mol, J. A. (1998). Behavioral, saliva cortisol and heart rate responses to different types of stimuli in dogs. Applied Animal Behaviour Science, 58(3–4), 365–381. https://doi.org/10.1016/S0168-1591(97)00145-7
Butler, R. K., & Finn, D. P. (2009). Stress-induced analgesia. Progress in Neurobiology, 88(3), 184–202. https://doi.org/10.1016/j.pneurobio.2009.04.003
Cooper, J. J., Cracknell, N., Hardiman, J., Wright, H., & Mills, D. S. (2014). The welfare consequences and efficacy of training pet dogs with remote electronic training collars in comparison to reward-based training. PLoS ONE, 9(9), e102722. https://doi.org/10.1371/journal.pone.0102722
Estes, W. K., & Skinner, B. F. (1941). Some quantitative properties of anxiety. Journal of Experimental Psychology, 29(5), 390–400. https://doi.org/10.1037/h0062283
Gray, J. A., & McNaughton, N. (2000). The Neuropsychology of Anxiety: An Enquiry into the Functions of the Septo-hippocampal System (2nd ed.). Oxford University Press.
Maier, S. F., & Seligman, M. E. P. (1976). Learned helplessness: Theory and evidence. Journal of Experimental Psychology: General, 105(1), 3–46. https://doi.org/10.1037/0096-3445.105.1.3
Schilder, M. B. H., & van der Borg, J. A. M. (2004). Training dogs with help of the shock collar: Short and long term behavioural effects. Applied Animal Behaviour Science, 85(3–4), 319–334. https://doi.org/10.1016/j.applanim.2003.10.004
Vieira de Castro, A. C., Fuchs, D., Morello, G. M., Pastur, S., de Sousa, L., & Olsson, I. A. S. (2020). Does training method matter? Evidence for the negative impact of aversive-based methods on companion dog welfare. PLoS ONE, 15(12), e0225023. https://doi.org/10.1371/journal.pone.0225023