Abstract
Underwater exposure imposes a distinctive cognitive burden because divers must maintain performance while environmental and physiological safety margins can change rapidly. Safe performance depends on attention, psychomotor speed, executive control, working memory, spatial orientation, metacognition, and decision-making, each of which may be influenced by pressure, breathing gases, respiratory load, immersion, thermal stress, fatigue, and individual susceptibility. Evidence from recreational, technical, breath-hold, and saturation diving remains difficult to synthesize because studies differ in exposure mode, gas composition, timing, task selection, ecological validity, and operational endpoints. This narrative state-of-the-art review addresses three questions: which stressors shape cognitive risk, how risk is currently assessed, and how selected signals might contribute to future context-aware estimation without adding unsafe task burden. We describe the literature-identification strategy, define cognitive risk as a probabilistic and baseline-referenced state rather than a single test abnormality, and map vulnerable domains to operational hazards such as delayed response, navigation error, unsafe gas decisions, missed alarms, and delayed recovery. We critically evaluate behavioral tasks, CFFF, EEG/ERP, HRV, electrodermal activity, NIRS, respiratory CO2 monitoring, and wearable platforms, emphasizing feasibility, signal quality, nonspecificity, synchronization, individualized baselines, and validation against operational outcomes. Finally, we propose a staged pathway from dry chamber validation to wet-chamber or planned-pause testing and then to occupational or saturation settings. Selected physiological and behavioral signals may contribute to cognitive-risk estimation only after transparent interpretation and prospective validation against meaningful endpoints.
1 Introduction
Underwater operations require cognition, physiology, and environmental control to remain coordinated under rapidly changing conditions. A diver must navigate, communicate, monitor life-support equipment, regulate buoyancy, interpret environmental cues, and maintain contingency plans while exposed to pressure, altered breathing gases, immersion, thermal stress, limited visibility, restricted movement, and limited escape options (Clark, 2015; Piispanen et al., 2021; Sharma et al., 2023). For recreational, military, occupational, technical, and saturation divers, even a small delay in attention, gas management, or emergency decision-making can be amplified by depth, decompression obligation, equipment complexity, respiratory burden, and team dependence (Hobbs et al., 2014; Freiberger et al., 2016; Dunworth et al., 2017; Dreyer et al., 2024).
Underwater cognition therefore differs from generic laboratory cognitive performance. Attention, working memory, inhibition, processing speed, situation awareness, workload, physiological state, and decision-making operate as a closed-loop system (Endsley, 1995; Wickens, 2008). Attention supports monitoring of depth, time, gas supply, buddy position, task progress, and unexpected change. Executive control suppresses unsafe responses under anxiety, overload, or narcosis, a function that appears vulnerable during underwater exposure (Karakaya et al., 2021). Working memory supports navigation, decompression planning, and procedural recall, whereas metacognitive accuracy is essential because divers may not reliably recognize their own impairment during inert gas narcosis (Germonpré et al., 2017). Cognitive decline underwater should therefore be viewed not only as a lower test score, but as reduced reliability, self-detection, and resilience of task-relevant control (Ergen et al., 2017; Lafère et al., 2019).
The evidence base has expanded. Recent studies and reviews have described cognitive function in scuba, technical, and saturation diving, including alertness, memory, decision-making, executive function, event-related potentials, and functional connectivity (Germonpré et al., 2017; Steinberg and Doppelmayr, 2017; Karakaya et al., 2021; Sharma et al., 2023; Vrijdag et al., 2022a). Extreme exposures remain difficult to study, but a 45 ATA simulated saturation dive reported impaired numerical Stroop performance even in expert divers (Kageyama and Sawamura, 2024). Taken together, these findings suggest that underwater cognitive vulnerability is measurable and exposure dependent, although not uniform across domains or paradigms.
The field remains fragmented. Studies differ in wet versus dry exposure, at-depth versus post-dive testing, breathing gas, exercise state, thermal condition, expertise, and cognitive endpoint. Monitoring approaches are equally diverse: CFFF is used as a low-burden index of central arousal (Lafère et al., 2019; Mankowska et al., 2021), EEG/ERP can capture neurofunctional changes (Karakaya et al., 2021; Vrijdag et al., 2022a), and HRV has been explored in relation to operational performance. No single tool currently provides a validated, continuously deployable, and operationally robust measure of underwater cognitive risk.
This review has both a review component and a perspective component. The review component summarizes cognitive domains, environmental determinants, and assessment tools. The perspective component proposes a conceptual monitoring framework that should be read as a research roadmap rather than operational guidance. We distinguish established observations, emerging hypotheses, and future research recommendations throughout. The overall conceptual logic is summarized in Figure 1.
Figure 1
2 Scope and approach of this review
This narrative, state-of-the-art review is intended for diving physiology, diving medicine, human factors, neuroergonomics, and extreme-environment research. It provides a structured interpretive synthesis and research roadmap rather than a systematic evidence grade or practice guideline. A systematic review or meta-analysis was not attempted because exposure mode, depth, gas composition, exercise state, timing, participant expertise, and cognitive outcomes vary widely. Instead, the review is organized around a translational question: how can underwater cognitive risk be understood and studied in ways that may eventually improve diving safety and operational performance?
PubMed/MEDLINE, Web of Science, Scopus, and Google Scholar were searched from database inception to May 2026. Search terms combined exposure terms (diving, scuba, technical diving, saturation diving, freediving, underwater exposure, hyperbaric chamber, immersion), stressor terms (nitrogen narcosis, hypercapnia, carbon dioxide, oxygen partial pressure, hyperoxia, gas density, cold exposure, workload, fatigue), cognitive terms (cognition, cognitive impairment, vigilance, reaction time, executive function, working memory, metacognition, decision-making), and monitoring terms (CFFF, EEG, ERP, HRV, EDA, NIRS, respiratory monitoring, wearable sensor, passive BCI, neuroergonomics). Reference lists of key reviews and mechanistic papers were also screened. Selection followed an iterative narrative-review process rather than blinded duplicate screening; no formal excluded-study log was generated. Priority was given to human diving or hyperbaric studies with clearly described exposure conditions, objective cognitive or operational outcomes, time-resolved or at-depth measurements, and monitoring relevance. Studies were de-emphasized when exposure was poorly characterized, the outcome was remote from diving safety, or the monitoring implication was not interpretable.
Because this is not a systematic review, no pooled estimate or formal risk-of-bias score was calculated. This narrative approach has important limitations: study selection was not blinded, contradictory findings could not be resolved statistically, and conclusions should be read as a structured synthesis rather than a definitive evidence hierarchy. Contradictory findings were interpreted by comparing exposure characterization, timing of assessment, cognitive-domain specificity, ecological validity, and linkage to operational outcomes rather than by vote counting. We also applied a practical hierarchy of interpretation: respiratory CO2 and breathing load were treated as high-priority monitoring targets because they have direct physiological and safety relevance; behavioral tasks provide objective but task-specific evidence; CFFF, EEG/ERP, HRV/EDA, and NIRS are adjunct signals that require context and endpoint validation; biological markers are mainly mechanistic or recovery-context evidence. Cognitive performance refers to observed task output, cognitive impairment to an observed decline on a defined task, cognitive readiness to pre-dive preparedness, and cognitive risk to the probability that a diver’s current environmental, physiological, and behavioral state will degrade task-relevant cognition before an overt error occurs. Thus, cognitive risk is a probabilistic latent operational state, an engineering prediction variable, and a safety metric rather than a clinical diagnosis. Operationally, it should be estimated from individualized baseline deviation, exposure load, respiratory burden, autonomic or neurofunctional strain, task phase, subjective state, and recovery trajectory: cognitive risk = f(baseline deviation, exposure load, respiratory burden, autonomic/neurofunctional strain, task phase, subjective state, prior recovery). Thresholds should be validated against operational outcomes, not assumed from universal cutoffs. Table 1 summarizes this evidence hierarchy and its interpretive limits.
Table 1
| Evidence cluster | Representative sources | Evidence strength in this review | Current inference | Main limitation | Interpretive use |
|---|---|---|---|---|---|
| CO2 and respiratory burden | Dunworth et al., 2017; Freiberger et al., 2016 | Relatively direct physiological and safety relevance | CO2 and breathing load are high-priority variables | CO2, effort, anxiety, and workload often co-vary | Measure when feasible and validate against performance |
| Behavioral task evidence | Dalecki et al., 2012; Steinberg and Doppelmayr, 2017; Kageyama and Sawamura, 2024 | Objective but task-specific | Selected domains can deteriorate during immersion or hyperbaric exposure | Tasks, timing, gas, and ecology are heterogeneous | Use as endpoint-specific probes, not global scores |
| Gas narcosis and metacognition | Hobbs et al., 2014; Germonpré et al., 2017; Vrijdag et al., 2022a | Moderate mechanistic and behavioral support | Narcosis may affect cognition and self-awareness | Wet/dry exposure and task differences limit generalization | Pair gas variables with domain-specific probes |
| CFFF | ; Lafère et al., 2019; Mankowska et al., 2026 | Adjunct arousal/neurofunctional evidence | Useful for low-burden state sampling | Not a global cognition measure; device and context dependent | Combine with tasks and exposure variables |
| EEG/ERP | Karakaya et al., 2021; Vrijdag et al., 2022a | Mechanistically informative in controlled settings | Can detect neurofunctional changes during hyperbaric exposure | Artifact, sensor, and ecological-validity constraints | Use primarily for chamber validation and selected field studies |
| HRV/EDA | Freiberger et al., 2024; Chen et al., 2025 | Contextual autonomic evidence | May index strain trends related to workload or stress | Nonspecific to cognition and affected by breathing/cold/exercise | Interpret with respiratory, thermal, and task labels |
| NIRS and breath-hold monitoring | Eichhorn et al., 2015; McKnight et al., 2021 | Useful in apnea and constrained contexts | Can track cerebral oxygenation trajectories | Sensor fixation, systemic physiology, and context specificity | Focus on hypoxia/apnea and recovery questions |
| Biological mechanisms | Vezzoli et al., 2024; ; Zhao et al., 2024a, Zhao et al., 2024b | Mechanistic and recovery-context evidence | May help explain susceptibility or prolonged effects | Does not validate real-time cognitive-risk monitoring in humans | Use for post-dive recovery and mechanistic research |
Evidence hierarchy and interpretive limits supporting the review framework.
3 Cognitive domains affected by underwater exposure
Cognitive performance underwater cannot be reduced to a single score. Different stressors may affect different domains, and the same exposure can impair one process while sparing, or transiently improving, another. Apparent contradictions across studies may therefore reflect domain specificity, testing time, and task selection rather than true inconsistency.
Attention and vigilance are central because divers monitor multiple dynamic variables while filtering irrelevant stimuli. Reduced vigilance can delay detection of gas problems, depth deviations, equipment malfunction, or buddy distress. Cold exposure and shallow immersion can affect attention and processing speed even without deep pressure exposure, and nitrogen narcosis may add distractibility, overconfidence, and reduced situation awareness (Dalecki et al., 2012; Falla et al., 2021).
Reaction time and psychomotor performance matter because many underwater tasks are time constrained. Simple reaction time is useful for repeated low-burden testing, whereas discrimination reaction time, tracking, and multitasking better approximate operational performance. Comparisons of reaction-time measures and CFFF indicate that motor speed, visual processing, and arousal are related but separable constructs (Tikkinen et al., 2016).
Executive function, including inhibitory control, cognitive flexibility, conflict monitoring, and planning, is especially operationally relevant. Divers at 20 m water depth showed selective executive-function impairment (Steinberg and Doppelmayr, 2017), and numerical Stroop testing detected changes during a 45 ATA simulated saturation dive (Kageyama and Sawamura, 2024). These paradigms are attractive because they probe conflict processing with relatively simple stimulus-response demands.
Executive vulnerability is not limited to one task or exposure model. Response-selection paradigms suggest that nitrogen narcosis can alter sensorimotor decision stages rather than simply slow motor output (Meckler et al., 2014). Across open-water and chamber studies, the most sensitive endpoint varies with depth, gas, timing, and task complexity, arguing against a single global cognition score (Tikkinen et al., 2016; ; Germonpré et al., 2017; Lafère et al., 2019).
Working memory supports navigation, decompression planning, equipment sequencing, and procedural recall. It is commonly assessed with digit span, Corsi block-tapping, n-back, and spatial tasks. Findings are inconsistent, probably because cognitive load, timing, and practice effects differ. Monitoring should therefore match the probe to the operational task rather than treat working memory as a universal marker.
Decision-making and metacognition are critical because divers must recognize when their own performance is deteriorating. Gas narcosis is hazardous when subjective confidence fails to decline with objective performance. Studies suggest that objective and subjective measures may not fully align during air or nitrox exposures (Hobbs et al., 2014; Germonpré et al., 2017), making impairment-awareness mismatch a relevant monitoring target.
Longer-term and repeated-exposure findings are harder to interpret. Some studies link diving exposure to neuropsychological, neurofunctional, or white-matter outcomes, whereas others are weaker or confounded by training, selection, decompression history, vascular risk, and exposure heterogeneity (Slosman et al., 2004; Hemelryck et al., 2014; ; Coco et al., 2019; Rosén et al., 2022). These data should not be overread as proof of chronic injury in all divers, but they justify longitudinal and recovery-focused designs.
3.1 Mapping cognitive domains to operational risk
A domain-to-risk mapping is needed because operational incidents rarely arise from one isolated cognitive function. Gas-management errors may combine attention to gauges, working-memory updating, metacognitive recognition of narrowing awareness, and decision-making under social or mission pressure. Navigation deviation may depend on spatial working memory and divided attention, whereas delayed alarm response may depend on vigilance, psychomotor speed, respiratory strain, and thermal stress. Future protocols should predefine the domain expected to contribute to each operational outcome.
This mapping also clarifies validation. A simple reaction-time probe may detect vigilance loss or psychomotor slowing, but it cannot validate a model intended to prevent unsafe gas decisions. Conversely, a short Stroop or response-inhibition probe may represent conflict monitoring but may be less sensitive to hand cooling or display constraints. Table 2 summarizes this mapping as a guide for future protocol design.
Table 2
| Cognitive domain | Operational risks | Candidate endpoint | Recommended probe or context |
|---|---|---|---|
| Vigilance/sustained attention | Missed alarm, delayed detection of gas or depth deviation, buddy-distress oversight | Missed signal rate; time to detect abnormal display or alarm | Brief vigilance probe; event detection during simulated monitoring |
| Reaction time/psychomotor speed | Delayed response to equipment, communication, or ascent/descent cues | Simple or choice reaction time; response delay to standardized cue | Low-burden repeated probe; separate motor and cognitive components when cold or gloves are present |
| Executive control | Unsafe impulse, poor inhibition under narcosis/anxiety, inappropriate emergency action | Stroop/interference cost; response-inhibition errors; rule violation | Short Stroop, Flanker, Simon, or go/no-go probe during chamber or planned pause |
| Working memory/spatial orientation | Navigation deviation, procedure omission, decompression-plan error | Route deviation; recall of gas/time plan; sequence error | Spatial span, n-back, route-memory, or procedure-recall probe matched to mission |
| Metacognition/decision-making | Failure to recognize impairment, overconfidence, unsafe gas or ascent decision | Mismatch between self-rating and objective performance; unsafe choice | Performance-confidence rating plus objective task and operational scenario |
Proposed mapping between cognitive domains and operational risk endpoints for future protocol design.
This mapping is intended to guide future protocols and requires validation before use in risk estimation or decision support.
4 Environmental determinants of cognitive risk
Table 3 summarizes the major environmental stressors, candidate mechanisms, affected domains, and monitoring implications discussed in this section.
Table 3
| Stressor | Diving context | Cognitive domains affected | Candidate mechanisms | Representative evidence | Monitoring implications | Priority |
|---|---|---|---|---|---|---|
| Depth/pressure | Scuba, technical, saturation | Executive control, reaction time, psychomotor performance | Increased gas partial pressures, gas density, decompression obligation | Steinberg and Doppelmayr, 2017; Kageyama and Sawamura, 2024 | Continuously label depth, pressure, phase, and decompression obligation | High |
| Nitrogen narcosis | Compressed-air and trimix diving | Judgment, memory, calculation, inhibitory control, metacognition | Inert gas effects on CNS function and network connectivity | Clark, 2015; Hobbs et al., 2014; Vrijdag et al., 2022a | Pair gas exposure with brief executive probes and EEG/CFFF where feasible | High |
| Gas composition | Air, nitrox, heliox, trimix | Error rate, arousal, cognitive-domain-specific effects | Narcotic potency, oxygen partial pressure, gas density | Germonpré et al., 2017; Lafère et al., 2019; Sharma et al., 2025 | Report partial pressures and gas density; avoid gas-label-only interpretation | Medium-high |
| Hypercapnia/respiratory burden | Exercise at depth, rebreathers, high-density gas | Attention, planning, psychomotor performance, situational awareness | CO2 retention, increased work of breathing, dyspnea, anxiety | Dunworth et al., 2017; Freiberger et al., 2016 | Prioritize CO2 and breathing-load monitoring when feasible | High |
| Oxygen partial pressure | Nitrox, HBO, rebreathers, saturation | Arousal, central excitability, task-specific performance | Hyperoxia, chemoreflex modulation, CNS oxygen toxicity risk | Vrijdag et al., 2022b; Möller et al., 2023 | Interpret arousal metrics with oxygen exposure and CNS toxicity risk in view | Context dependent |
| Cold immersion | Open-water and polar/temperate diving | Attention, processing speed, executive function, dexterity-mediated performance | Thermal stress, discomfort, peripheral cooling, arousal changes | Falla et al., 2021; Piispanen et al., 2021 | Combine thermal, manual-performance, workload, and cognitive measures | Context dependent |
| Workload and fatigue | Operational, military, rescue, prolonged operations | Vigilance, decision-making, multitasking, working memory | Exercise, sleep loss, cumulative stress, fatigue | Möller et al., 2021, Möller et al., 2023 | Use phase labels, workload ratings, fatigue measures, and longitudinal baselines | High in prolonged work |
| Breath-hold hypoxia/hypercapnia | Freediving | Executive control, awareness, hypoxic blackout risk | Apnea, cerebral oxygenation changes, blood-gas shifts | McKnight et al., 2021; Paganini et al., 2026 | Integrate NIRS/SpO2, apnea phase, symptoms, and recovery trajectory | High in freediving |
Environmental stressors and cognitive implications during underwater exposure.
4.1 Hyperbaric pressure and depth
Depth is the most visible determinant of underwater risk, but cognitive effects arise through several pathways: gas partial pressures, gas density, work of breathing, decompression obligation, thermal exchange, and equipment complexity. Depth is therefore useful operationally, but effects attributed to depth may actually reflect gas, respiratory load, or task context.
At recreational and technical depths, compressed-air diving increases nitrogen partial pressure and may induce inert gas narcosis. At extreme depths, saturation exposure adds confinement and cumulative physiological load. A simulated 440 m sea-water saturation dive at 45 ATA found impaired numerical Stroop performance in expert divers, suggesting that training does not eliminate hyperbaric cognitive vulnerability (Kageyama and Sawamura, 2024).
Technical diving adds complexity because gas choice, decompression obligation, equipment configuration, bailout planning, and task loading change simultaneously. Future studies should therefore report depth and pressure together with gas composition, inspired partial pressures, estimated gas density, exercise state, temperature, and task demands. Without these details, depth-related cognitive effects remain difficult to interpret.
4.2 Inert gas narcosis and breathing-gas composition
Nitrogen narcosis can affect reasoning, memory, calculation, judgment, mood, motor behavior, and self-awareness, with risk generally increasing with depth during compressed-air diving. Its operational hazard is not only performance decline, but also reduced recognition of decline while safety-critical decisions continue (Clark, 2015).
Neurophysiological studies provide mechanistically informative, but context-limited, evidence. Auditory ERP changes during simulated 500 kPa air exposure and EEG functional-connectivity changes during air breathing at 608 kPa suggest altered cognitive processing under hyperbaric nitrogen (Karakaya et al., 2021; Vrijdag et al., 2022a). These findings support EEG/ERP as research tools, but not yet as deployable operational monitors.
Breathing-gas composition may modify cognitive risk through narcotic potency, gas density, oxygen partial pressure, and respiratory mechanics. Air, nitrox, heliox, and trimix are not interchangeable exposures. Open-water and chamber studies indicate gas-specific effects, but differences in inspired partial pressures, task timing, and subjective state limit direct comparison (; Germonpré et al., 2017; Sharma et al., 2025).
Future studies should report gas composition quantitatively rather than categorically. Inspired partial pressures, gas density, and breathing resistance are likely more informative than labels such as air, nitrox, or trimix, especially when comparing dry chambers with wet dives.
Nitrox illustrates this caution. It may reduce venous gas bubbles in selected simulated protocols (Souday et al., 2016), but decompression advantage should not be conflated with a validated cognitive benefit across all tasks and depths.
4.3 Hypercapnia, respiratory burden, and gas density
Carbon dioxide retention is a major determinant of underwater cognitive risk. Hypercapnia can arise from elevated inspired CO2, scrubber failure, dead space, inadequate ventilation, high gas density, breathing resistance, exercise, or behavioral suppression of breathing. It can escalate rapidly and may interact with anxiety, dyspnea, and oxygen-toxicity risk (Dunworth et al., 2017).
CO2 effects are not identical to nitrogen or oxygen effects. Hyperbaric studies indicate that N2, CO2, and O2 can affect attention, memory, planning, and psychomotor outcomes differently (Fothergill et al., 1991; Freiberger et al., 2016; Gill et al., 2014). CO2 should therefore be measured where feasible rather than inferred from symptoms alone.
Respiratory burden links physiology to cognition. Increased gas density and resistance can raise breathing effort, promote CO2 retention, increase anxiety, and reduce spare attentional capacity. Inspired or expired CO2, ventilation, respiratory rate, work of breathing, and gas density should be recorded whenever feasible, particularly in rebreather, technical, and high-workload dives.
A key research need is to separate hypercapnia from effort. Cognitive risk may reflect elevated CO2, high physical workload, or both. Combining respiratory monitoring with brief cognitive probes and autonomic signals could help identify when respiratory burden becomes cognitively consequential.
4.4 Oxygen partial pressure, hyperoxia, and central excitability
Oxygen is neither simply protective nor harmful. Inspired oxygen partial pressure varies with depth and breathing mixture, and its cognitive effects depend on level, duration, susceptibility, and interaction with nitrogen, CO2, and workload. Higher oxygen partial pressure may reduce inert gas fraction in some mixtures, but hyperoxia can also alter central excitability and increase oxygen-toxicity risk in susceptible contexts (Wingelaar et al., 2017; Ciarlone et al., 2019; Vrijdag et al., 2022b).
Oxygen-related neural effects may be misread as improved alertness, reduced narcosis, or emerging hyperexcitability depending on the outcome measured. CFFF studies under normobaric and hyperbaric oxygen suggest arousal changes, but not simple cognitive enhancement (Sharma et al., 2024).
High oxygen partial pressure should not be assumed to improve cognition uniformly. Oxygen exposure should be modeled as a state variable when interpreting CFFF, EEG, subjective alertness, or cognitive probes during oxygen-rich decompression, rebreather use, or hyperoxic exercise.
4.5 Cold immersion and thermal stress
Cold exposure can degrade cognition through discomfort, pain, altered arousal, motor impairment, distraction, and changes in skin and core temperature. It may impair attention, processing speed, executive function, and memory (Falla et al., 2021), while also reducing dexterity, display interaction, regulator comfort, and task persistence.
Cold is also an indirect cognitive stressor because it can increase perceived workload, breathing discomfort, and fatigue. Arctic and cold-water diving studies highlight the need to report temperature, exposure duration, suit type, hand cooling, and task type alongside cognitive outcomes (Piispanen et al., 2021).
Immersion itself is not neutral. Five-meter water immersion can impair overall cognitive performance, sustained attention, and tracking, and task complexity may influence the size of the deficit (Dalecki et al., 2012). These findings caution against attributing all effects to gas or pressure.
For monitoring, thermal and immersion variables should be integrated rather than treated as nuisance factors. A slowed response during cold-water tool use may reflect cognitive slowing, hand cooling, visibility, stress, or their combination.
4.6 Physical workload, fatigue, and prolonged underwater operations
Exercise has bidirectional effects on cognition. In general exercise science, acute exercise may modestly improve selected executive-function or reaction-time outcomes, but effects depend on intensity, task, timing, and training status (Chang et al., 2012; McMorris and Hale, 2012; Ludyga et al., 2016; Garrett et al., 2024). Underwater exercise is different because it can increase CO2 production, ventilation demand, breathing discomfort, perceived exertion, fatigue, and attentional narrowing, especially with immersion, equipment load, increased gas density, or breathing resistance (Freiberger et al., 2016; Dunworth et al., 2017; Pattyn et al., 2018). Studies of submersion and hyperoxic underwater exercise show that cognitive responses may differ from dry laboratory expectations (Möller et al., 2021, Möller et al., 2023).
Fatigue may be more important than acute task load in prolonged operations, but it is harder to measure. It includes physical fatigue, sleep restriction, cumulative stress, repeated decompression demands, and psychological strain. In saturation diving, confinement, altered sleep, noise, social stress, and long exposure windows may produce fluctuations not captured by single pre- and post-dive tests (Sharma et al., 2023; Kageyama and Sawamura, 2024). Broader fatigue research suggests that cognitive and physical fatigue interact through perceived exertion, self-regulation, and sustained attention (Marcora et al., 2009; Van Cutsem et al., 2017; Pattyn et al., 2018).
Workload assessment should be explicit. NASA-TLX can separate mental demand, physical demand, temporal demand, effort, performance, and frustration (Hart and Staveland, 1988; Hart, 2006). In diving, these dimensions may diverge: a chamber task can impose high mental demand with little movement, whereas current-exposed work can impose high physical and respiratory demand with secondary cognitive effects. Workload reports should be paired with objective markers such as exercise intensity, ventilation, respiratory rate, CO2, heart rate, HRV, task duration, sleep history, and environmental exposure.
4.7 Saturation diving and confined hyperbaric exposure
Saturation diving combines depth, duration, confinement, sleep disruption, decompression time, team dependence, and constrained working conditions. Simulated 45 ATA saturation exposure has been associated with impaired cognitive performance, while commercial-diver studies highlight the importance of subjective state, fatigue, and chamber environment (Imbert et al., 2018; Kageyama and Sawamura, 2024).
Saturation studies are limited by small samples, logistical barriers, and difficulty standardizing exposure. This supports the rationale for continuous low-burden sampling, but also means that chamber environmental records, sleep/activity monitoring, brief executive probes, HRV, respiratory indicators, and subjective fatigue reports require prospective validation before operational use.
4.8 Breath-hold diving and hypoxia-related risk
Breath-hold diving should be treated separately from scuba and saturation diving. Dominant stressors include apnea, hypoxia, hypercapnia, hydrostatic pressure, bradycardia, peripheral vasoconstriction, cerebral blood-flow redistribution, and sometimes decompression stress. Recent reviews emphasize rapid blood-gas changes, neurovascular responses, and persistent knowledge gaps (Tetzlaff et al., 2021; Paganini et al., 2026). NIRS work in elite freedivers illustrates feasibility of cerebral oxygenation monitoring under specialized conditions (McKnight et al., 2021).
Freediving is useful for monitoring development because hypoxia and hypercapnia evolve rapidly and can be measured alongside neurofunctional signals. Event-related EEG and NIRS studies show that prolonged breath-holding or deep breath-hold dives can modulate neurocognitive and cerebral-oxygenation markers in experienced divers (Eichhorn et al., 2015; Steinberg and Doppelmayr, 2019; McKnight et al., 2021).
The apnea literature also emphasizes individual reserve and adaptation. Spleen and lung volumes predict apnea performance (Schagatay et al., 2012), and freedivers may show distinctive cerebral metabolism, cerebrovascular reactivity, vascular adaptation, or antioxidant responses during repeated hypoxic-hypercapnic exposure (Sureda et al., 2015; Tanaka et al., 2016; Vestergaard and Larsson, 2019). These adaptations should not be generalized uncritically to scuba or saturation diving.
For this review, breath-hold diving provides both a model of extreme physiological compensation and a reminder that monitoring thresholds are context specific. Mechanisms from freediving should not be transferred directly to compressed-gas or saturation diving.
Swimming and aquatic-exercise research reinforces this systems view: immersion, exercise, breathing pattern, and aquatic posture can influence cerebrovascular and cognitive function even outside compressed-gas diving (Shoemaker et al., 2019).
5 Assessment methods for underwater-related cognitive risk
Table 4 summarizes candidate cognitive assessment tools, their advantages, limitations, and feasible use contexts.
Table 4
| Tool/task | Target domain | Advantages | Limitations | Underwater feasibility | Best-use scenario/recommended use |
|---|---|---|---|---|---|
| Simple reaction time | Psychomotor speed | Brief, repeatable, easy to automate | Practice effects; motor contamination; low domain specificity | High | Repeated low-burden probe for trend detection |
| Discrimination/tracking tasks | Sensorimotor coordination, sustained attention | Closer to operational performance | Affected by dexterity, visibility, and equipment | Moderate | Controlled chamber or field protocols emphasizing operational performance |
| Stroop/Simon/Flanker | Inhibitory control and conflict processing | Sensitive to executive changes; feasible in chambers | Requires display-response reliability; practice effects | Moderate | Core executive probe for chamber, wet, or planned-pause testing |
| Digit span/Corsi/n-back | Verbal and spatial working memory | Domain-specific; compact | May be less sensitive than RT/executive measures in some exposures | Moderate | Navigation, planning, or procedure-heavy missions |
| MATB-II or micro-MATB | Multitasking and operational performance | Higher ecological validity | Longer, more complex, harder underwater | Low to moderate | Model training and validation in chambers or simulators |
| CFFF | Visual processing/cortical arousal proxy | Simple and portable | Confounded by illumination, method, age, ocular factors; not global cognition | Moderate | Adjunct arousal signal within multimodal assessment, not a global cognition proxy |
| Waterproof digital testing | Multiple domains | Potential for in-water assessment | Interface reliability, glove use, pressure/waterproofing | Emerging | Field feasibility studies after interface validation |
Cognitive assessment tools used in diving and hyperbaric studies.
5.1 Behavioral cognitive tasks
Behavioral tests remain the foundation of cognitive assessment because they are interpretable, inexpensive, and directly related to task performance. Reaction-time tasks are brief and repeatable; Stroop tasks assess conflict processing; digit span, Corsi, n-back, and spatial tasks assess working memory; and tracking or dual-task paradigms approximate motor-cognitive coordination. Tasks should be chosen according to the cognitive domain most relevant to the mission.
Behavioral tasks also have limitations. Practice effects, motor slowing, hand cooling, display visibility, glove use, buoyancy, and touchscreen reliability can contaminate interpretation. Post-dive testing may miss transient at-depth impairment or introduce recovery effects, whereas at-depth testing may interfere with safety. Protocols should therefore use brief, robust, domain-specific probes with repeated baselines and automated quality-control flags.
5.2 Stroop and executive-function paradigms
Stroop-type paradigms assess inhibitory control and conflict processing with simple stimuli. Their use at 20 m water depth and during simulated 45 ATA saturation exposure supports feasibility across different contexts (Steinberg and Doppelmayr, 2017; Kageyama and Sawamura, 2024). The challenge is to keep probes short enough for safety while retaining sensitivity to meaningful deterioration.
5.3 Multitasking and operational-performance batteries
Operational performance underwater is inherently multitask: divers track depth, time, gas, communication, navigation, body position, and task progress. Multitasking batteries therefore offer greater ecological validity than isolated tasks. MATB-II-like frameworks, which include tracking, monitoring, communication, and resource management, are especially relevant when physiological monitoring is linked to operational performance rather than isolated cognitive scores (Freiberger et al., 2024).
5.4 Critical flicker fusion frequency
CFFF is widely used in diving and hyperbaric research because it is simple, non-invasive, and repeatable. It is often interpreted as a marker of cortical arousal or central nervous system alertness (Mankowska et al., 2021). Studies using CFFF under different gas mixtures and after scuba diving explain why it remains attractive for field research (; Lafère et al., 2019).
Its interpretation should be restrained. CFFF is best treated as a complementary neurofunctional index rather than a substitute for cognitive testing. It enables repeated low-burden sampling of arousal state, but is affected by instructions, illumination, device characteristics, circadian state, learning, ocular factors, and threshold definition (Mankowska et al., 2021, Mankowska et al., 2026; Muth et al., 2026).
Recent work reinforces this caution. Oxygen exposure can alter CFFF responses across normobaric and hyperbaric conditions, and correlations between CFFF components and executive or memory measures appear variable (Sharma et al., 2024; Mankowska et al., 2025, Mankowska et al., 2026). Thus, CFFF meaning depends on gas, light, device, participant, and task context.
Accordingly, CFFF should be combined with exposure data, brief cognitive probes, and physiological signals rather than used as a stand-alone proxy for global cognition.
5.5 Underwater-compatible digital testing
Digital testing can bridge laboratory neuropsychology and operational monitoring. Waterproof tablets or pressure-tolerant interfaces could allow short cognitive probes during chamber exposures or planned underwater pauses. A recent case study identified feasibility but also practical limits in stimulus presentation and touch-response reliability (Yoshimura and Takahashi, 2025). Future systems need glove-compatible interfaces, high-contrast displays, low burden, timing calibration, and physiological-data integration.
5.6 Timing, baselines, and interpretation
Assessment timing strongly shapes interpretation. Pre-dive testing captures fatigue, sleep, anxiety, and baseline readiness; in-dive testing captures acute exposure effects but is constrained by safety; immediate post-dive testing may detect residual effects; and delayed testing may reflect recovery, fatigue, or decompression-related symptoms (Dreyer et al., 2024). Rigorous protocols should include repeated individualized baselines, exposure-phase labels, and explicit handling of learning effects.
6 Physiological and neurofunctional monitoring strategies
Table 5 summarizes the main physiological and neurofunctional monitoring approaches, including their signals, limitations, and current status.
Table 5
| Monitoring method | Signal type | Target risk | Strengths | Limitations | Current status |
|---|---|---|---|---|---|
| EEG | Neurofunctional connectivity, spectral dynamics, ERP components | Nitrogen narcosis, cortical arousal, stimulus processing | Direct brain-state information | Setup burden, artifacts, waterproofing, pressure tolerance | High mechanistic value; operational readiness remains early |
| ERP | P300/MMN-like indices of cognitive processing | Attention and stimulus evaluation | Objective and domain interpretable | Needs controlled stimuli; artifacts | Useful for validation; limited immediate in-dive readiness |
| HRV | Autonomic regulation | Stress, workload, fatigue, impaired performance risk | Wearable, continuous, low burden | Nonspecific; affected by breathing, cold, exercise | Useful for contextual trend monitoring within multimodal models |
| EDA | Sympathetic arousal | Stress and workload | Continuous, complementary to HRV | Water and motion challenges; nonspecific | Adjunct workload/stress signal; interpretation depends on context |
| NIRS/fNIRS | Cerebral oxygenation/hemodynamics | Hypoxia, cerebral stress, frontal activation | Useful in breath-hold and chamber contexts | Waterproofing, motion, hair, pressure effects | High for hypoxia/apnea questions; water deployment remains constrained |
| Respiratory CO2/ventilation | Inspired or expired CO2, breathing pattern | Hypercapnia and respiratory burden | Targets a known critical risk | Sensor integration and calibration underwater | High practical relevance when reliable sensing is available |
| Wearable platforms | Multisensor fusion | General cognitive-risk estimation | Scalable and longitudinal | Validation, data quality, interpretability | Research-stage; useful only after endpoint validation |
Physiological and neurofunctional monitoring approaches.
6.1 EEG and event-related potentials
EEG is mechanistically valuable because it measures neurofunctional state directly, but most evidence remains chamber-based, proof-of-concept, or dependent on controlled stimuli. Functional connectivity at 608 kPa air exposure and auditory ERP changes during simulated hyperbaric nitrogen exposure suggest sensitivity to nitrogen narcosis and altered stimulus processing (Karakaya et al., 2021; Vrijdag et al., 2022a). These findings support EEG/ERP as research tools; they do not establish deployable in-dive monitoring or direct identification of cognitive impairment.
Field translation requires waterproofing, pressure tolerance, electrical safety, electrode stability, limited setup time, artifact control, ecological validity, and timely interpretability. A chamber signal is not automatically useful during a working dive with movement, bubbles, equipment noise, thermal stress, and task switching. EEG and ERP are therefore among the most informative mechanistic tools, but remain constrained for continuous operational use.
Signal-quality control should be a core requirement. In diving-relevant EEG/ERP, motion, ocular and facial-muscle artifacts, regulator or mask movement, electrode displacement, perspiration, pressure effects, water sealing, cable movement, and equipment noise can mimic or obscure neurocognitive effects. Wearable EEG improves portability but may reduce channel count, sampling flexibility, and artifact tolerance. Out-of-lab artifact-correction and wearable-EEG benchmarking work shows the need for online artifact management, device comparison, and neurometric reliability checks (Ronca et al., 2024, Ronca et al., 2026a).
EEG protocols should report electrode type, fixation, impedance or contact-quality criteria, sampling rate, filtering, artifact correction, retained data percentage, synchronization, and whether features were computed from artifact-free windows only. Any EEG-derived alarm should include signal-confidence flags and validation against prespecified task or operational endpoints.
6.2 HRV, electrodermal activity, and autonomic markers
Autonomic markers are attractive because they can be measured continuously and non-invasively. HRV reflects autonomic regulation, workload, stress, breathing patterns, and recovery state. Diving studies suggest associations between HRV features, operational performance, and physiological stress responses, but HRV should be used within multimodal models rather than as a stand-alone cognitive marker (Freiberger et al., 2024; Chen et al., 2025).
General HRV methodology supports caution because indices are strongly affected by respiration, posture, workload, stress, and recovery state (Laborde et al., 2017; Shaffer and Ginsberg, 2017). In underwater settings, these influences are part of the operational state. HRV is most useful when modeled with breathing pattern, CO2 risk, workload, temperature, and task performance.
EDA may complement HRV by indexing sympathetic arousal, but neither HRV nor EDA should be treated as a direct marker of cognitive impairment. Autonomic changes may reflect cognitive strain, emotion, cold, hypercapnia, exercise, pain, anxiety, breathing pattern, recovery, or equipment discomfort. Their value lies in synchronization with dive phase, respiratory variables, thermal exposure, workload, subjective state, and task performance (Ronca et al., 2026b).
6.3 NIRS and cerebral oxygenation
NIRS can monitor cerebral oxygenation and hemodynamics, especially in frontal regions relevant to executive control, but it does not directly measure cognition. It has been used during deep breath-hold diving in elite freedivers (McKnight et al., 2021), and may be useful in breath-hold, dry hyperbaric, or limited-movement chamber contexts. Barriers in scuba and occupational diving include sensor fixation, pressure tolerance, motion artifacts, water sealing, hair interference, thermal stress, equipment interference, and interpretation under changing oxygen and CO2 levels.
Interpretation requires care. fNIRS signals are affected by extracerebral blood flow, motion, optode placement, hair, and systemic physiology (Pinti et al., 2020). Diving amplifies these limitations because pressure, water sealing, facial equipment, exercise, and CO2 can all influence cerebral and peripheral hemodynamics.
NIRS should be viewed as a cerebral-state signal rather than a direct cognitive test. Reduced cerebral oxygenation may indicate hypoxic risk, but stable oxygenation does not guarantee preserved executive function. Like HRV, NIRS becomes useful when combined with exposure data and brief cognitive probes.
6.4 Respiratory CO2 monitoring and breathing-load assessment
Respiratory monitoring is one of the strongest candidates for future underwater cognitive-risk research because CO2 retention and breathing load have direct physiological and safety relevance. CO2 retention can arise from equipment failure, high work of breathing, exercise, or behavioral patterns and can rapidly degrade mental and physical performance (Dunworth et al., 2017). Inspired CO2, end-tidal CO2, ventilation, respiratory rate, gas density, and work of breathing would directly address a known safety threat, but sensor robustness and equipment integration remain major constraints.
Because subjective symptoms may not detect CO2-related cognitive risk early enough, respiratory metrics should be incorporated into future estimation models when feasible. A diver with rising CO2, increasing respiratory effort, deteriorating HRV, and slowed reaction time represents a different risk state from isolated mild slowing after repetitive testing, but this combined interpretation still requires prospective endpoint validation.
6.5 Wearable platforms and multimodal risk estimation
Wearable technology is expanding in diving, including devices for breath-hold applications, heart rate, and oxygen saturation (Vinetti et al., 2020; Bube et al., 2022; ; Park et al., 2025). For cognitive risk, however, physiological signals must be validated against task-relevant cognitive and operational outcomes.
The next step is not simply to add sensors. A useful system must define what each signal means, when it should be interpreted as potentially relevant, and how false alarms will be controlled. Without such validation, wearable monitoring risks becoming data-rich but operationally weak.
A proposed architecture could include environmental exposure data, physiological signals, and brief cognitive probes. Environmental data include depth, pressure, phase, gas, temperature, and workload proxies; physiological signals may include HRV, respiratory variables, EEG-derived metrics, NIRS, EDA, and oxygen saturation; cognitive probes should be short and domain specific. As outlined in Figure 2, these streams would require data-quality checks and individualized baselines before contributing to risk estimates. Such systems might eventually support continued monitoring, workload reduction, gas switch, ascent, rest, or post-dive recovery restriction, but only after prospective validation.
Figure 2
6.6 Feasibility staging for underwater monitoring
Feasibility differs substantially across settings. Dry hyperbaric chambers are suitable for mechanism testing and synchronized EEG/ERP or NIRS recording, but cannot reproduce movement, buoyancy, visibility, thermal, and equipment constraints. Wet chambers and planned underwater pauses can test waterproof interfaces, display-response reliability, and brief probes with lower safety risk. Continuous open-water or occupational monitoring is currently most realistic for passive exposure data, respiratory variables, heart rate or HRV, and selected low-burden wearable outputs; continuous EEG/ERP/NIRS remains research-stage unless signal quality and safety are demonstrated.
A method feasible during a decompression stop may be inappropriate during navigation, rescue, tool use, current exposure, or emergency ascent. Future studies should label each method as feasible now, chamber-only, feasible during planned underwater pauses, or speculative for continuous real-dive deployment. Table 6 summarizes the corresponding feasibility and validation considerations.
Table 6
| Component | Near-term feasible setting | Main constraints | Core validation endpoint |
|---|---|---|---|
| Exposure and equipment data | Continuous open-water, chamber, and saturation settings | Synchronization and standardized phase labels | Depth/phase-linked association with operational events |
| Brief cognitive probes | Dry chamber, wet chamber, planned underwater pauses | Practice effects, interface reliability, safety burden | Meaningful within-diver change; response delay; error rate |
| CFFF | Chamber and selected field protocols | Illumination, ocular factors, device thresholds | Arousal-state change as adjunct, not global cognition |
| HRV/EDA | Continuous passive monitoring | Nonspecificity: exercise, cold, CO2, anxiety, pain, recovery | Context-aware strain trends with respiratory and task labels |
| Respiratory CO2/breathing load | High priority when sensor integration is reliable | Sensor calibration, water sealing, dead space, equipment integration | Hypercapnia or breathing-load risk; relation to performance decline |
| EEG/ERP | Dry chamber; experimental wet settings; limited real-dive deployment | Waterproofing, pressure, artifacts, electrode stability, safety | Signal-quality-controlled association with attention/executive outcomes |
| NIRS/fNIRS | Freediving, chamber, and controlled underwater protocols | Fixation, hair, motion, systemic physiology, waterproofing | Cerebral oxygenation trajectory and recovery, especially apnea/hypoxia |
| Wearable fusion model | Research-stage; staged validation required | Data quality, synchronization, individual baselines, false alarms | Association with task failure, unsafe decision, navigation deviation, missed alarm, or delayed recovery |
Feasibility and validation considerations for candidate monitoring components.
The matrix summarizes feasible testing settings, key constraints, and candidate validation endpoints that should be addressed before operational implementation.
6.7 Relation to passive BCI and neuroergonomics
The framework aligns with passive brain-computer interface and neuroergonomics research, which infers operator state from neurophysiological and physiological signals without deliberate commands. These fields have developed methods for monitoring workload, vigilance, stress, mental effort, and operator capacity in aviation, driving, surgery, and industry (; ; Zhou et al., 2022). Diving shares the need for state estimation but adds pressure, immersion, respiratory constraints, water sealing, and limited interfaces. Underwater monitoring should borrow validation logic from these fields while avoiding direct transfer of thresholds from dry or seated tasks.
A useful underwater system should be transparent and operator centered. It should indicate whether risk is driven by respiratory burden, environmental exposure, autonomic strain, cognitive-probe deterioration, poor signal confidence, or their combination. Without interpretability, multimodal fusion may increase false alarms and distrust rather than improve safety.
7 Emerging biological mechanisms
This review is not primarily mechanistic, and biological mechanisms should be interpreted as context for susceptibility, recovery, and prolonged effects rather than as evidence for real-time cognitive-risk monitoring in human divers. Diving physiology involves pressure, gas kinetics, vascular responses, oxidative stress, decompression stress, and inflammatory responses (; Vezzoli et al., 2024). Dopamine/BDNF findings may offer a neurochemical bridge between narcosis-related physiology and cognition, although operational interpretation remains preliminary ().
The redox-vascular literature is relevant mainly to recovery, resilience, and repeated exposure. Diving can produce adverse stress responses or adaptive physiological responses depending on exposure profile, fitness, and recovery state (Perovic et al., 2014). Biomarkers should therefore be interpreted as context-dependent indicators of load and adaptation rather than simple evidence of injury.
Saturation and scuba studies have reported oxidative-stress biomarker changes across prolonged or depth-varying exposures (Mrakic-Sposta et al., 2020; Marchetti et al., 2022). These markers are not cognitive tests, but they may help explain recovery differences, prolonged fatigue, symptoms, or delayed readiness for complex tasks.
Field studies provide systemic context rather than direct cognitive-monitoring validation. Repeated or deep dives can be accompanied by endothelial dysfunction, oxidative stress, vascular gas emboli, and antioxidant responses, and integrated physiological-biochemical monitoring is feasible in real dive settings (Obad et al., 2010; Sureda et al., 2012; Marinovic et al., 2012; ). These findings do not directly measure cognition, but they support including vascular and biological context when recovery or repeated exposure is a concern.
Vascular and neuroinflammatory pathways are emerging but should be interpreted cautiously. Decompression stress, endothelial activation, microbubbles, cerebral oxygenation changes, and blood-brain barrier vulnerability may contribute to post-dive symptoms or longer-term effects in susceptible contexts. Animal studies suggest pathways linking prolonged underwater stress, hippocampal vulnerability, microglial activation, and cognition, but should not be overgeneralized to human divers (Zhao et al., 2024a, Zhao et al., 2024b).
Immediate task performance may not fully capture biological burden, but current biological evidence does not justify real-time human cognitive-risk classification. Future studies should test whether physiological monitoring, biochemical markers, and cognitive recovery curves can improve post-dive risk assessment.
8 Practical implications and future directions
8.1 Pre-dive screening
Pre-dive assessment may need to move beyond general medical fitness in occupational or research contexts. Sleep, fatigue, stress, anxiety, medication, dehydration, prior dives, recent illness, and sensitivity to narcosis or CO2 can affect cognitive readiness. A short baseline battery covering reaction time, executive control, and subjective fatigue could contextualize in-dive or post-dive changes, but individualized thresholds require validation.
8.2 In-dive monitoring
In-dive monitoring must be low burden and should not distract from safety-critical tasks. The most realistic near-term approach is passive exposure and physiological monitoring, with brief cognitive probes only during planned pauses or chamber intervals. Systems should flag patterns that justify attention, workload reduction, or post-dive reassessment, not issue black-box operational commands.
8.3 Post-dive recovery assessment
Post-dive monitoring matters because impairment may persist after surfacing. Residual narcosis, vascular gas emboli, fatigue, and inflammatory or oxidative responses may affect recovery (Dreyer et al., 2024; ). Post-dive tests should distinguish transient at-depth impairment, decompression-related symptoms, fatigue, and delayed recovery.
8.4 Standardization and validation
A standardized underwater cognitive-risk battery should include a small number of tasks covering vigilance, reaction time, executive control, and working memory, plus subjective fatigue and workload. The battery should be brief, repeatable, device-stable, and usable across dry chambers, wet chambers, and field conditions; it should support comparison rather than replace mission-specific assessment.
8.5 Toward individualized cognitive-risk estimation
Individualized cognitive-risk estimation is a future goal rather than a current operational capability. Divers differ in fitness, experience, anxiety, ventilatory response, narcosis susceptibility, cold tolerance, sleep, and learning effects. Machine-learning models may eventually integrate exposure, physiology, and performance, but require large, well-labeled datasets, transparent features, and validation against meaningful endpoints. Interpretability is essential; black-box scores without confidence or driver information should not guide safety-critical decisions.
8.6 Ideal study methodology
An ideal future study would be staged, prospective, and validation oriented. Stage 1 would establish repeated dry baselines across separate days to quantify intra-individual variability, practice effects, sleep/fatigue influences, and device reliability. Outputs would include stable baseline distributions for reaction time, executive control, vigilance, workload, HRV, respiratory variables, and any EEG/NIRS features.
Stage 2 would use controlled dry hyperbaric chamber exposures with standardized pressure, gas mixture, inspired partial pressures, CO2 or ventilation load, temperature, workload, and testing time. The goal would be feasibility, signal quality, domain sensitivity, and dose-response characterization, not operational deployment.
Stage 3 would test only components that passed stage-2 feasibility and signal-quality criteria in wet-chamber or open-water trials. Cognitive probes should be brief, prespecified, and limited to planned pauses. Waterproofing, display readability, response reliability, glove use, buoyancy, motion artifacts, and workload interference would become primary endpoints.
Stage 4 would evaluate occupational or saturation settings for longitudinal reliability, recovery curves, false-alarm burden, user acceptance, and decision usefulness. Core validation outcomes should include task failure, response delay, navigation deviation, gas-management error, unsafe ascent/descent behavior, missed alarm, expert-rated performance, abnormal recovery, and restriction from safety-sensitive work.
8.7 Research roadmap and priority areas
Figure 3 translates the discussion into a staged roadmap. The field does not need more unrelated tests; it needs comparable protocols that connect exposure, physiology, cognition, and operational outcome. A minimal core dataset should include participant expertise, exposure profile, gas variables, CO2/respiratory burden, thermal exposure, workload, cognitive probes, physiological signal quality, and operational endpoints.
Figure 3
A staged strategy would reduce the gap between laboratory and field research. Chamber studies suit mechanism and signal validation; wet-chamber and open-water studies test usability and ecological validity; saturation or occupational studies are needed for longitudinal reliability and decision usefulness. Each stage should have explicit stop/go criteria before a tool is treated as operationally informative.
8.8 Research gaps and reporting standards
Several gaps remain urgent: real underwater studies are fewer than chamber studies; deep and saturation studies are necessarily small; CO2, workload, sleep, and thermal variables are often underreported; and few studies link signals to operational endpoints. Most importantly, multimodal signals have not yet been prospectively validated for safety-critical cognitive-risk classification. This limitation should guide interpretation of the proposed framework.
A practical reporting standard would improve comparability. Future studies should report participant expertise, pressure profile, wet/dry exposure, gas and inspired partial pressures, estimated gas density, CO2 and respiratory variables, temperature, workload, timing of cognitive tests, baseline procedures, device characteristics, signal-quality criteria, and operational endpoints. This would allow future systematic reviews or meta-analyses to distinguish robust findings from context-specific effects.
9 Conclusion
Underwater cognitive risk is a multidimensional physiological, neurofunctional, and operational problem shaped by pressure, gases, nitrogen narcosis, CO2 retention, oxygen partial pressure, immersion, cold, workload, fatigue, and individual susceptibility. Cognitive performance, cognitive impairment, cognitive readiness, and cognitive risk should be distinguished: impairment is observed task decline, whereas risk is a probabilistic, baseline-referenced state that may precede overt error.
The main contribution of this review is to organize current evidence and outline a staged research roadmap for underwater cognitive-risk assessment and monitoring. Future work should move from isolated pre- and post-dive tests toward integrated, context-aware, staged validation. Environmental exposure data, respiratory and autonomic measures, selected neurofunctional signals, and brief cognitive probes may become useful when quality controlled, synchronized, interpreted against individualized baselines, and evaluated against operational endpoints. Figures 1-3 and Tables 2, 6 are intended to support protocol design and should be tested prospectively before operational use. Multimodal fusion should not be assumed to solve the problem automatically; its value will depend on transparency, feasibility, signal quality, ecological validity, and prospective validation.
Statements
Author contributions
HZ: Writing – original draft, Writing – review & editing, Investigation, Conceptualization. LW: Writing – review & editing, Writing – original draft, Conceptualization. YZ: Writing – original draft, Conceptualization, Writing – review & editing. NZ: Writing – review & editing. SZ: Writing – review & editing. YW: Writing – review & editing. XY: Funding acquisition, Conceptualization, Project administration, Writing – review & editing, Supervision. YF: Project administration, Supervision, Writing – review & editing, Funding acquisition, Conceptualization.
Funding
The author(s) declared that financial support was received for this work and/or its publication. This work was supported by the Discipline Development Program in Diving Medicine, the “Strengthening Foundation Program” of the Naval Medical Specialty Center, the Military Science Program of the National Social Science Fund of China, and the Naval Weapon and Equipment Pre-research Unit (3020201020102).
Conflict of interest
The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declared that generative AI was used in the creation of this manuscript. AI-assisted tools (Deepseek-V4, China) were used solely for graphical rendering based on author-designed schematics. All figures were critically reviewed and verified by the authors to ensure scientific accuracy. Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.
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References
1
BagheriM.PowerS. D. (2022). Simultaneous classification of both mental workload and stress level suitable for an online passive brain-computer interface. Sensors22, 535. doi: 10.3390/s22020535
2
BalestraC.LafèreP.GermonpréP. (2012). Persistence of critical flicker fusion frequency impairment after a 33 mfw SCUBA dive: evidence of prolonged nitrogen narcosis? Eur. J. Appl. Physiol.112, 4063–4068. doi: 10.1007/s00421-012-2391-z
3
BalestraC.LévêqueC.Mrakic-SpostaS.VezzoliA.WauthyP.GermonpréP.et al. (2024). Physiology of deep closed circuit rebreather mixed gas diving: vascular gas emboli and biological changes during a week-long liveaboard safari. Front. Physiol.15, 1395846. doi: 10.3389/fphys.2024.1395846
4
Bast-PettersenR.SkareØCheckt. a. e.NordbyK. C.SkogstadM. (2015). A twelve-year longitudinal study of neuropsychological function in non-saturation professional divers. Int. Arch. Occup. Environ. Health88, 669–682. doi: 10.1007/s00420-014-0991-0
5
BeattyP.EvansW.GravelynS.TumperiM.DaubonD.VeithA. (2024). Physiological monitoring to prevent diving disorders. Front. Physiol.15, 1517361. doi: 10.3389/fphys.2024.1517361
6
BorghiniG.AricòP.Di FlumeriG.RoncaV.GiorgiA.SciaraffaN.et al. (2022). Air Force pilot expertise assessment during unusual attitude recovery flight. Safety8, 38. doi: 10.3390/safety8020038
7
BoscoG.GiaconT. A.PaolocciN.VezzoliA.NoceC. D.PaganiniM.et al. (2023). Dopamine/BDNF loss underscores narcosis cognitive impairment in divers: a proof of concept in a dry condition. Eur. J. Appl. Physiol.123, 143–158. doi: 10.1007/s00421-022-05055-6
8
BoscoG.RizzatoA.MoonR. E.CamporesiE. M. (2018). Environmental physiology and diving medicine. Front. Psychol.9, 72. doi: 10.3389/fpsyg.2018.00072
9
BrebeckA. K.DeussenA.Schmitz-PeifferH.RangeU.BalestraC.ClevelandS.et al. (2017). Effects of oxygen-enriched air on cognitive performance during SCUBA-diving - an open-water study. Res. Sport. Med.25, 345–356. doi: 10.1080/15438627.2017.1314289
10
BubeB.ZanónB. B.Lara PalmaA. M.KlockeH. (2022). Wearable devices in diving: scoping review. JMIR Mhealth. Uhealth.10, e35727. doi: 10.2196/35727
11
ChangY. K.LabbanJ. D.GapinJ. I.EtnierJ. L. (2012). The effects of acute exercise on cognitive performance: a meta-analysis. Brain Res.1453, 87–101. doi: 10.1016/j.brainres.2012.02.068
12
ChenY. J.TzengY. S.TangS. E.LiC. R.WuS. Y.HuangK. L. (2025). Autonomic and physiological stress responses in navy divers: the protective role of diving experience. Front. Physiol.16, 1642779. doi: 10.3389/fphys.2025.1642779
13
CiarloneG. E.HinojoC. M.StavitzskiN. M.DeanJ. B. (2019). CNS function and dysfunction during exposure to hyperbaric oxygen in operational and clinical settings. Redox Biol.27, 101159. doi: 10.1016/j.redox.2019.101159
14
ClarkJ. E. (2015). Moving in extreme environments: inert gas narcosis and underwater activities. Extrem. Physiol. Med.4, 1. doi: 10.1186/s13728-014-0020-7
15
CocoM.BuscemiA.PerciavalleV.MaciT.GalvanoG.ScavoneA. M. F.et al. (2019). Cognitive deficits and white matter alterations in highly trained scuba divers. Front. Psychol.10, 2376. doi: 10.3389/fpsyg.2019.02376
16
DaleckiM.BockO.SchulzeB. (2012). Cognitive impairment during 5 m water immersion. J. Appl. Physiol. (1985).113, 1075–1081. doi: 10.1152/japplphysiol.00825.2012
17
DreyerS.SchneppendahlJ.HoffmannsM.MuthT.SchipkeJ. D. (2024). Narcotic nitrogen effects persist after a simulated deep dive. Med. (Kaunas).60 (7), 1083. doi: 10.3390/medicina60071083
18
DunworthS. A.NatoliM. J.CooterM.CherryA. D.PeacherD. F.PotterJ. F.et al. (2017). Hypercapnia in diving: a review of CO2 retention in submersed exercise at depth. Undersea. Hyperb. Med.44, 191–209. doi: 10.22462/5.6.2017.1
19
EichhornL.ErdfelderF.KesslerF.DoernerJ.ThudiumM. O.MeyerR.et al. (2015). Evaluation of near-infrared spectroscopy under apnea-dependent hypoxia in humans. J. Clin. Monit. Comput.29, 749–757. doi: 10.1007/s10877-015-9662-2
20
EndsleyM. R. (1995). Toward a theory of situation awareness in dynamic systems. Hum. Factors37, 32–64. doi: 10.1518/001872095779049543
21
ErgenM.UsluA.CaglarO.Akca-KalemS.CimsitM.GurvitH. (2017). Evaluation of cognitive performance in professional divers by means of event-related potentials and neuropsychology. Clin. Neurophysiol.128, 579–588. doi: 10.1016/j.clinph.2017.01.007
22
FallaM.MicarelliA.HüfnerK.StrapazzonG. (2021). The effect of cold exposure on cognitive performance in healthy adults: a systematic review. Int. J. Environ. Res. Public Health18 (18), 9725. doi: 10.3390/ijerph18189725
23
FothergillD. M.HedgesD.MorrisonJ. B. (1991). Effects of CO2 and N2 partial pressures on cognitive and psychomotor performance. Undersea. Biomed. Res.18, 1–19.
24
FreibergerJ.DerrickB.ChonK. H.HossainM. B.Posada-QuinteroH. F.CooterM.et al. (2024). Does heart rate variability predict impairment of operational performance in divers? Sensors. (Basel).24 (23), 7726. doi: 10.3390/s24237726
25
FreibergerJ. J.DerrickB. J.NatoliM. J.AkushevichI.SChinaziE. A.ParkerC.et al. (2016). Assessment of the interaction of hyperbaric N2, CO2, and O2 on psychomotor performance in divers. J. Appl. Physiol. (1985).121, 953–964. doi: 10.1152/japplphysiol.00534.2016
26
GarrettJ.ChakC.BullockT.GiesbrechtB. (2024). A systematic review and Bayesian meta-analysis provide evidence for an effect of acute physical activity on cognition in young adults. Commun. Psychol.2, 82. doi: 10.1038/s44271-024-00124-2
27
GermonpréP.BalestraC.HemelryckW.BuzzacottP.LafèreP. (2017). Objective vs. subjective evaluation of cognitive performance during 0.4-MPa dives breathing air or nitrox. Aerosp. Med. Hum. Perform.88, 469–475. doi: 10.3357/amhp.4608.2017
28
GillM.NatoliM. J.VacchianoC.MacLeodD. B.IkedaK.QinM.et al. (2014). Effects of elevated oxygen and carbon dioxide partial pressures on respiratory function and cognitive performance. J. Appl. Physiol. (1985).117, 406–412. doi: 10.1152/japplphysiol.00995.2013
29
HartS. G. (2006). NASA-task load index (NASA-TLX); 20 years later. Proc. Hum. Factors. Ergon. Soc Annu. Meet.50, 904–908. doi: 10.1177/154193120605000909
30
HartS. G.StavelandL. E. (1988). Development of NASA-TLX (Task Load Index): results of empirical and theoretical research. In: HancockP. A.MeshkatiN., editors. Human Mental Workload. (Amsterdam: North-Holland), 139–183. doi: 10.1016/S0166-4115(08)62386-9
31
HemelryckW.GermonpréP.PapadopoulouV.RozloznikM.BalestraC. (2014). Long term effects of recreational SCUBA diving on higher cognitive function. Scand. J. Med. Sci. Sport.24, 928–934. doi: 10.1111/sms.12100
32
HobbsM.HighamP. A.KnellerW. (2014). Memory and metacognition in dangerous situations: investigating cognitive impairment from gas narcosis in undersea divers. Hum. Factors.56, 696–709. doi: 10.1177/0018720813510737
33
ImbertJ. P.BalestraC.KiboubF. Z.LoennechenØ.EftedalI. (2018). Commercial divers' subjective evaluation of saturation. Front. Psychol.9, 2774. doi: 10.3389/fpsyg.2018.02774
34
KageyamaN.SawamuraT. (2024). Effect of hyperbaric exposure on cognitive performance: an investigation conducting numerical Stroop tasks during a simulated 440 m sea water saturation diving. J. Physiol. Anthropol.43, 24. doi: 10.1186/s40101-024-00366-3
35
KarakayaH.AksuS.EgiS. M.AydinS.UsluA. (2021). Effects of hyperbaric nitrogen narcosis on cognitive performance in recreational air SCUBA divers: an auditory event-related brain potentials study. Ann. Work. Expo. Health65, 505–515. doi: 10.1093/annweh/wxaa132
36
LabordeS.MosleyE.ThayerJ. F. (2017). Heart rate variability and cardiac vagal tone in psychophysiological research - recommendations for experiment planning, data analysis, and data reporting. Front. Psychol.8, 213. doi: 10.3389/fpsyg.2017.00213
37
LafèreP.HemelryckW.GermonpréP.MatityL.GuerreroF.BalestraC. (2019). Early detection of diving-related cognitive impairment of different nitrogen-oxygen gas mixtures using critical flicker fusion frequency. Diving. Hyperb. Med.49, 119–126. doi: 10.28920/dhm49.2.119-126
38
LudygaS.GerberM.BrandS.Holsboer-TrachslerE.PühseU. (2016). Acute effects of moderate aerobic exercise on specific aspects of executive function in different age and fitness groups: a meta-analysis. Psychophysiology53, 1611–1626. doi: 10.1111/psyp.12736
39
MankowskaN. D.MarcinkowskaA. B.WaskowM.SharmaR. I.KotJ.WinklewskiP. J. (2021). Critical flicker fusion frequency: a narrative review. Med. (Kaunas).57 (10), 1096. doi: 10.3390/medicina57101096
40
MankowskaN. D.SharmaR. I.MarcinkowskaA. B.KotJ.WinklewskiP. J. (2025). Assessing the relationship between the flicker test and cognitive performance. Biology14, 1469. doi: 10.3390/biology14111469
41
MankowskaN. D.SharmaR. I.MarcinkowskaA. B.WinklewskiP. J.KotJ. (2026). Complex relationship between critical flicker fusion frequency and established cognitive tests unveiled by hyperbaric exposure. Biol. (Basel).15 (3), 242. doi: 10.3390/biology15030242
42
MarchettiE.PiginiD.SpagnoliM.TranfoG.BuonaurioF.SciubbaF.et al. (2022). Hyperbaric exposure of scuba divers affects the urinary excretion of nucleic acid oxidation products and hypoxanthine. Int. J. Environ. Res. Public Health19 (5), 3005. doi: 10.3390/ijerph19053005
43
MarcoraS. M.StaianoW.ManningV. (2009). Mental fatigue impairs physical performance in humans. J. Appl. Physiol. (1985).106, 857–864. doi: 10.1152/japplphysiol.91324.2008
44
MarinovicJ.LjubkovicM.BreskovicT.GunjacaG.ObadA.ModunD.et al. (2012). Effects of successive air and nitrox dives on human vascular function. Eur. J. Appl. Physiol.112, 2131–2136. doi: 10.1007/s00421-011-2187-6
45
McKnightJ. C.MulderE.RueschA.KainerstorferJ. M.WuJ.HakimiN.et al. (2021). When the human brain goes diving: using near-infrared spectroscopy to measure cerebral and systemic cardiovascular responses to deep, breath-hold diving in elite freedivers. Philos. Trans. R. Soc Lond. B. Biol. Sci.376, 20200349. doi: 10.1098/rstb.2020.0349
46
McMorrisT.HaleB. J. (2012). Differential effects of differing intensities of acute exercise on speed and accuracy of cognition: a meta-analytical investigation. Brain Cognit.80, 338–351. doi: 10.1016/j.bandc.2012.09.001
47
MecklerC.BlatteauJ. E.HasbroucqT.SchmidB.RissoJ. J.VidalF. (2014). Effects of hyperbaric nitrogen-induced narcosis on response-selection processes. Ergonomics57, 210–218. doi: 10.1080/00140139.2013.877161
48
MöllerF.HoffmannU.DaleckiM.DrägerT.DoppelmayrM.SteinbergF. (2021). Physical exercise intensity during submersion selectively affects executive functions. Hum. Factors.63, 227–239. doi: 10.1177/0018720819879313
49
MöllerF.JacobiE.HoffmannU.VogtT. (2023). Physiological and cognitive responses to hyperoxic exercise in full water submersion. Eur. J. Sport. Sci.23, 1647–1657. doi: 10.1080/17461391.2023.2193942
50
Mrakic-SpostaS.VezzoliA.D'AlessandroF.PaganiniM.DellanoceC.CialoniD.et al. (2020). Change in oxidative stress biomarkers during 30 days in saturation dive: a pilot study. Int. J. Environ. Res. Public Health17 (19), 7118. doi: 10.3390/ijerph17197118
51
MuthT.SchipkeJ. D.BrebeckA. K.DreyerS. (2026). Critical flicker fusion frequency: confounders and caveats. Eur. J. Appl. Physiol.126, 725–734. doi: 10.1007/s00421-025-05935-7
52
ObadA.MarinovicJ.LjubkovicM.BreskovicT.ModunD.BobanM.et al. (2010). Successive deep dives impair endothelial function and enhance oxidative stress in man. Clin. Physiol. Funct. Imaging30, 432–438. doi: 10.1111/j.1475-097X.2010.00962.x
53
PaganiniM.MoonR. E.CamporesiE. M.BoscoG. (2026). Advances in breath-hold diving research: a state-of-the-art review. Eur. J. Appl. Physiol.126, 1223–1243. doi: 10.1007/s00421-025-06093-6
54
ParkT. S.KimM. G.ParkJ. H.HongJ. M.LeeD.HanI. H.et al. (2025). Wearable technology in diving: a review of heart rate and oxygen saturation monitoring for enhanced safety and performance. Healthc. (Basel).13 (18), 2346. doi: 10.3390/healthcare13182346
55
PattynN.Van CutsemJ.DessyE.MairesseO. (2018). Bridging exercise science, cognitive psychology, and medical practice: is "cognitive fatigue" a remake of "the emperor's new clothes"? Front. Psychol.9, 1246. doi: 10.3389/fpsyg.2018.01246
56
PerovicA.UnicA.DumicJ. (2014). Recreational scuba diving: negative or positive effects of oxidative and cardiovascular stress? Biochem. Med. (Zagreb).24, 235–247. doi: 10.11613/bm.2014.026
57
PiispanenW. W.LundellR. V.TuominenL. J.Räisänen-SokolowskiA. K. (2021). Assessment of alertness and cognitive performance of closed circuit rebreather divers with the critical flicker fusion frequency test in arctic diving conditions. Front. Physiol.12, 722915. doi: 10.3389/fphys.2021.722915
58
PintiP.TachtsidisI.HamiltonA.HirschJ.AichelburgC.GilbertS.et al. (2020). The present and future use of functional near-infrared spectroscopy (fNIRS) for cognitive neuroscience. Ann. N. Y. Acad. Sci.1464, 5–29. doi: 10.1111/nyas.13948
59
RoncaV.Castagneto GisseyL.BelliniM. I.IodiceA.SadaV.SbardellaE.et al. (2026b). Multi-method characterization of neurophysiological and biological stress responses in surgical teams during real surgical procedures. Front. Neuroergonomics.7, 1702748. doi: 10.3389/fnrgo.2026.1702748
60
RoncaV.CecchettiM.CapotortoR.Di FlumeriG.GiorgiA.GermanoD.et al. (2026a). Beyond the lab: real-world benchmarking of wearable EEGs for passive brain-computer interfaces. Brain Inf.13, 3. doi: 10.1186/s40708-025-00290-x
61
RoncaV.Di FlumeriG.GiorgiA.VozziA.CapotortoR.GermanoD.et al. (2024). o-CLEAN: a novel multi-stage algorithm for the ocular artifacts' correction from EEG data in out-of-the-lab applications. J. Neural Eng.21, 056023. doi: 10.1088/1741-2552/ad7b78
62
RosénA.GennserM.OscarssonN.KvarnströmA.SandströmG.Seeman-LoddingH.et al. (2022). Protein tau concentration in blood increases after SCUBA diving: an observational study. Eur. J. Appl. Physiol.122, 993–1005. doi: 10.1007/s00421-022-04892-9
63
SchagatayE.RichardsonM. X.Lodin-SundströmA. (2012). Size matters: spleen and lung volumes predict performance in human apneic divers. Front. Physiol.3, 173. doi: 10.3389/fphys.2012.00173
64
ShafferF.GinsbergJ. P. (2017). An overview of heart rate variability metrics and norms. Front. Public Health5, 258. doi: 10.3389/fpubh.2017.00258
65
SharmaR. I.MankowskaN. D.MarcinkowskaA. B.WinklewskiP. J.KotJ. (2024). Critical flicker fusion frequency results during oxygen decompression in standard HBOT session - observational study. Int. Marit. Health75, 167–176. doi: 10.5603/imh.99568
66
SharmaR. I.MankowskaN. D.MarcinkowskaA. B.WinklewskiP. J.KotJ. (2025). Heliox at 4 ATA reduces error rates compared to trimix and air, but it does not affect short-term memory in hyperbaric conditions. Biol. (Basel).14 (12), 1748. doi: 10.3390/biology14121748
67
SharmaR. I.MarcinkowskaA. B.MankowskaN. D.WaśkowM.KotJ.WinklewskiP. J. (2023). Cognitive functions in scuba, technical and saturation diving. Biol. (Basel).12 (2), 229. doi: 10.3390/biology12020229
68
ShoemakerL. N.WilsonL. C.LucasS. J. E.MaChadoL.ThomasK. N.CotterJ. D. (2019). Swimming-related effects on cerebrovascular and cognitive function. Physiol. Rep.7, e14247. doi: 10.14814/phy2.14247
69
SlosmanD. O.De RibaupierreS.ChicherioC.LudwigC.MontandonM. L.AllaouaM.et al. (2004). Negative neurofunctional effects of frequency, depth and environment in recreational scuba diving: the Geneva "memory dive" study. Br. J. Sport. Med.38, 108–114. doi: 10.1136/bjsm.2002.003434
70
SoudayV.KoningN. J.PerezB.GrelonF.MercatA.BoerC.et al. (2016). Correction: Enriched air nitrox breathing reduces venous gas bubbles after simulated SCUBA diving: a double-blind cross-over randomized trial. PloS One11, e0165771. doi: 10.1371/journal.pone.0165771
71
SteinbergF.DoppelmayrM. (2017). Executive functions of divers are selectively impaired at 20-meter water depth. Front. Psychol.8, 1000. doi: 10.3389/fpsyg.2017.01000
72
SteinbergF.DoppelmayrM. (2019). Neurocognitive markers during prolonged breath-holding in freedivers: an event-related EEG study. Front. Physiol.10, 69. doi: 10.3389/fphys.2019.00069
73
SuredaA.BatleJ. M.FerrerM. D.Mestre-AlfaroA.TurJ. A.PonsA. (2012). Scuba diving activates vascular antioxidant system. Int. J. Sport. Med.33, 531–536. doi: 10.1055/s-0031-1297957
74
SuredaA.BatleJ. M.TurJ. A.PonsA. (2015). Competitive apnea diving sessions induces an adaptative antioxidant response in mononucleated blood cells. J. Physiol. Biochem.71, 373–380. doi: 10.1007/s13105-015-0417-9
75
TanakaH.TomotoT.KosakiK.SugawaraJ. (2016). Arterial stiffness of lifelong Japanese female pearl divers. Am. J. Physiol. Regul. Integr. Comp. Physiol.310, R975–R978. doi: 10.1152/ajpregu.00048.2016
76
TetzlaffK.LemaitreF.BurgstahlerC.LuetkensJ. A.EichhornL. (2021). Going to extremes of lung physiology-deep breath-hold diving. Front. Physiol.12, 710429. doi: 10.3389/fphys.2021.710429
77
TikkinenJ.WuorimaaT.SiimesM. A. (2016). A comparison of simple reaction time, visual discrimination and critical flicker fusion frequency in professional divers at elevated pressure. Diving. Hyperb. Med.46, 82–86.
78
Van CutsemJ.MarcoraS.De PauwK.BaileyS.MeeusenR.RoelandsB. (2017). The effects of mental fatigue on physical performance: a systematic review. Sport. Med.47, 1569–1588. doi: 10.1007/s40279-016-0672-0
79
VestergaardM. B.LarssonH. B. (2019). Cerebral metabolism and vascular reactivity during breath-hold and hypoxic challenge in freedivers and healthy controls. J. Cereb. Blood Flow Metab.39, 834–848. doi: 10.1177/0271678x17737909
80
VezzoliA.Mrakic-SpostaS.BrizzolariA.BalestraC.CamporesiE. M.BoscoG. (2024). Oxy-inflammation in humans during underwater activities. Int. J. Mol. Sci.25 (5), 3060. doi: 10.3390/ijms25053060
81
VinettiG.LopomoN. F.TaboniA.FagoniN.FerrettiG. (2020). The current use of wearable sensors to enhance safety and performance in breath-hold diving: a systematic review. Diving. Hyperb. Med.50, 54–65. doi: 10.28920/dhm50.1.54-65
82
VrijdagX. C. E.van WaartH.PullonR. M.SamesC.MitchellS. J.SleighJ. W. (2022a). EEG functional connectivity is sensitive for nitrogen narcosis at 608 kPa. Sci. Rep.12, 4880. doi: 10.1038/s41598-022-08869-8
83
VrijdagX. C. E.van WaartH.SamesC.MitchellS. J.SleighJ. W. (2022b). Does hyperbaric oxygen cause narcosis or hyperexcitability? A quantitative EEG analysis. Physiol. Rep.10, e15386. doi: 10.14814/phy2.15386
84
WickensC. D. (2008). Multiple resources and mental workload. Hum. Factors.50, 449–455. doi: 10.1518/001872008x288394
85
WingelaarT. T.van OoijP. A. M.van HulstR. A. (2017). Oxygen toxicity and special operations forces diving: hidden and dangerous. Front. Psychol.8, 1263. doi: 10.3389/fpsyg.2017.01263
86
YoshimuraN.TakahashiK. (2025). Evaluating tablet-based cognitive testing in underwater environments: a case study with two divers. i-com24, 601–611. doi: 10.1515/icom-2025-0020
87
ZhaoH.LiangK.YuZ.WenY.ShiJ.ZhangT.et al. (2024b). Hyperbaric oxygen preconditioning rescues prolonged underwater exercise-induced hippocampal dysfunction by regulating microglia activation and polarization. Neurosci. Res.207, 26–36. doi: 10.1016/j.neures.2024.05.004
88
ZhaoH.LiangK.YuZ.WenY.YuX.XinJ.et al. (2024a). CCR3 knockdown attenuates prolonged underwater operations-induced cognitive impairment via alleviating microglia-mediated neuroinflammation. iScience27, 110379. doi: 10.1016/j.isci.2024.110379
89
ZhouY.HuangS.XuZ.WangP.WuX.ZhangD. (2022). Cognitive workload recognition using EEG signals and machine learning: a review. IEEE Trans. Cognit. Dev. Syst.14, 799–818. doi: 10.1109/TCDS.2021.3090217
Summary
Keywords
cognitive impairment, context-aware monitoring, critical flicker fusion frequency, diving physiology, EEG, heart rate variability, underwater exposure
Citation
Zhao H, Wang L, Zhao Y, Zhao N, Zhang S, Wang Y, Yu X and Fang Y (2026) Cognitive risk during underwater exposure: from environmental stressors to assessment and context-aware monitoring. Front. Physiol. 17:1888182. doi: 10.3389/fphys.2026.1888182
Received
22 May 2026
Revised
19 July 2026
Accepted
23 July 2026
Published
07 August 2026
Volume
17 - 2026
Edited by
Costantino Balestra, Haute École Bruxelles-Brabant (HE2B), Belgium
Reviewed by
Alessandro Marroni, DAN Europe Foundation, Malta
Vincenzo Ronca, Sapienza University of Rome, Italy
Annette Schmidt, Munich University of the Federal Armed Forces, Germany
Clément Leveque, University of North Carolina at Chapel Hill, United States
Updates
Copyright
© 2026 Zhao, Wang, Zhao, Zhao, Zhang, Wang, Yu and Fang.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yan Wang, 616485882@qq.com; Xuhua Yu, xuhua_0813@163.com; Yiqun Fang, 1287225836@qq.com
†These authors have contributed equally to this work
Disclaimer
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