The next seven powers—without pretending they are finished.
These definitions are implementation-ready research candidates. They cannot be assessed, scored, averaged or transferred into the frozen Core. Promotion requires the evidence, safety, accessibility and adversarial checks shown below.
One lane inside the internal programme: the Candidate Lab is not the Titan Research & Governance Lab itself and is not a separate public product. It is the bounded testing lane within that subordinate programme, using the same master register, provenance-preserving archive and promotion process as the Observatory, hostile review, Personal Science and future research waves.
Separate method layer: Personal Science & Responsible Biohacking is not an eighth Candidate module and cannot be promoted by a personal result. It governs how low-risk comparisons are recorded while clinical, emerging and rejected claims stay in their proper lanes.
Candidate evolution · no automatic promotion
These candidates can improve while their lane stays locked.
Definitions, evidence maps, counter-evidence, measurement, safety and accessibility can all evolve internally. Titan records those changes separately from permission to explain, permission to guide, an external-confirmation requirement and independent validation. None of the seven candidates gains a score or operational status from internal progress alone.
Task-level control of avoidable interruptions, deliberate switching and resumption on one declared real-work task under recorded conditions.
Does not establish
No general attention, intelligence, productivity or ADHD-treatment claim. Deep-work duration alone is not evidence of quality. Safety-critical monitoring, caregiving, driving and emergency-response work are excluded from notification blocking.
Direct
Predeclare one primary task measure: median resumption lag from interruption end to first correct primary-task action; matched-block task-switch cost in time and errors; or protected-session completion rate with an objective task-quality floor. Record at least three comparable baseline and three comparison sessions.
Retention
Repeat the same task and interruption script without live coaching after at least 7 days; use the original primary measure and quality floor.
Transfer
Use a predeclared second real-work task or a different interruption source of comparable risk and difficulty; preserve the task-quality floor.
Burden
Minutes spent configuring the system, fatigue, frustration, anxiety, missed important alerts, delayed communication, accessibility cost and any fall in task quality.
Protocol and evidence gates
Choose one meaningful, non-safety-critical task and define a correct unit of work.
List interrupt sources and classify each as critical, time-bounded or deferrable; critical alerts always remain available.
Run at least three baseline sessions with a fixed task window and a declared interruption script.
Configure one low-burden intervention: notification batching, a visible focus boundary, a single-task queue, or a pre-switch resumption cue containing current state and next action.
Run at least three matched comparison sessions and record time, errors, completed units, resumption lag and burden.
Keep, adapt or retire the intervention based on the primary outcome, quality floor and burden rather than subjective busyness.
Repeat after at least seven days without live coaching, then run the predeclared transfer task.
L1A recorded baseline exists, but focus sessions, resumption or task quality are inconsistent or require substantial external support.
L2A narrow interruption-control routine improves the practised task only with reminders, protected conditions or active support.
L3The predeclared direct criterion and task-quality floor are met in two comparable sessions with no missed critical alert.
L4The L3 result survives the delayed retest and the predeclared transfer criterion is met on a second safe task or interruption source.
L5Performance remains reliable across at least three declared work constraints, and the person can create and explain a safe interruption plan for another nonclinical task without claiming general attention enhancement.
Safety, clinical, jurisdiction and accessibility guardrails
safety
Never silence alarms or alerts required for health, safeguarding, caregiving, security, transport or emergency response.
Do not run interruption experiments while driving, using machinery, administering medication or supervising a dependent person.
Stop if the intervention produces missed critical communication, unsafe hyperfocus, severe fatigue, pain or escalating distress.
clinical
This module neither diagnoses nor treats ADHD or another clinical condition.
Medication, sleep and treatment changes are outside scope and belong with a qualified clinician.
Persistent functional impairment or distress routes to appropriate professional assessment rather than a higher practice dose.
jurisdiction
Respect workplace monitoring, recording, availability, safeguarding and employment requirements.
Do not record other people's communications or personal data without a lawful basis and informed permission.
accessibility
Permit visual, auditory, haptic or assistive resumption cues and flexible session lengths.
Record all supports without treating assistive technology, a support person or an ADHD-friendly environment as a penalty.
Offer low-sensory and low-motor alternatives, rest breaks and asynchronous communication where the task permits.
Promotion gates
Validate the resumption-lag and task-quality data fields in the Universal Module Lab.
Pilot the protocol on at least two different real-work task types without safety-critical alert suppression.
Demonstrate that the direct metric cannot be passed by doing less work or lowering quality.
Accessibility review must include neurodivergent, fatigue-limited, screen-reader and motor-access routes.
Clinical wording review must confirm that no ADHD-treatment or general attention claim is implied.
In a controlled knowledge-work simulation, interruptions changed work behaviour and increased reported stress, frustration, time pressure and effort even when participants compensated with faster work. Limit: A small laboratory simulation, not an intervention trial or evidence of a general focus-improvement protocol; faster completion did not mean a universal productivity gain.
Preparation during an interruption warning interval and goal encoding can shorten resumption disruption on a defined experimental task. Limit: Artificial dynamic task and controlled interruption timing; does not establish transfer to all work, treatment of ADHD or a durable general attention change.
Four experiments found measurable time costs when participants switched between task rules rather than repeating one rule. Limit: Laboratory classification and arithmetic tasks; establishes a switch-cost phenomenon, not the effectiveness of a specific workplace routine or general executive-function training.
02 · MOD-ADHERENCE-HABITCANDIDATE · UNSCORED
Self-Regulation & Sustainable Performance
Adherence & Habit Formation
Design and test low-risk cue, environment and recovery systems that increase completion of one precisely defined behaviour under declared conditions.
Does not establish
No willpower score, moral judgement, universal habit-formation timetable or treatment claim. Medication, glucose, diet, substance use, self-harm, compulsive behaviour and clinically prescribed rehabilitation targets require the relevant professional pathway.
Direct
Externally verifiable completion rate: completed eligible opportunities divided by all predeclared eligible opportunities. Also record cue-to-action latency and recovery after a miss. Self-reported automaticity is secondary and cannot by itself earn L3.
Retention
Measure at least 14 consecutive days after the initial supported phase, including at least 7 days with prompts reduced to the predeclared maintenance level.
Transfer
Apply the same design process to a predeclared second low-risk behaviour with a different cue or context; set its criterion before starting.
Burden
Setup and tracking time, financial cost, rigidity, distress after misses, conflict with sleep or care, symptom change, privacy exposure and opportunity cost.
Protocol and evidence gates
Select one small, low-risk behaviour and define what counts, what does not count and when an opportunity is ineligible.
Record a baseline using an external trace where practical; do not reconstruct missed days from memory.
Write one if-then plan linked to an observable cue and identify the most likely obstacle.
Reduce friction for the desired action, increase friction for the competing action and create a minimum viable version for low-capacity days.
Track completions, eligible opportunities, misses, recovery time and burden without streak punishment.
After the supported phase, reduce prompts to the predeclared maintenance level and run the delayed test.
Apply the same design process to the predeclared second low-risk behaviour for transfer.
L1A baseline exists, but the defined behaviour is inconsistent, eligible opportunities are missed or completion depends on substantial support.
L2Completion improves on the practised behaviour while reminders, environmental support or accountability remain active.
L3The externally supported direct criterion is met across the full declared interval at acceptable burden.
L4The criterion survives the reduced-prompt delayed interval and the predeclared transfer behaviour meets its criterion.
L5The design remains reliable across at least three declared disruptions, includes a safe recovery-from-miss rule and can be explained or taught without prescribing clinical behaviour or promising automaticity.
Safety, clinical, jurisdiction and accessibility guardrails
safety
Do not reward sleep loss, pain escalation, skipped care, unsafe exercise, food restriction, medication changes or compulsive repetition.
Never use shame, financial coercion, public exposure or punishment for a miss.
Stop or redesign if rigidity, distress, conflict, symptom worsening or unsafe persistence increases.
Across varied studies, if-then implementation intentions improved goal attainment, with a historic aggregate estimate near d = 0.65. Limit: The synthesis combines heterogeneous laboratory and field outcomes; later reviews of objective behaviours often find smaller effects, so the historic aggregate is not a promised individual gain.
A meta-analysis of 21 articles comprising 24 independent field studies (15,907 participants) found a small-to-medium aggregate benefit for mental contrasting with implementation intentions (g = 0.336). Limit: This is a combined intervention rather than implementation intentions alone; intervention style moderated results and publication bias may make the true effect smaller.
Repeated performance of a chosen behaviour in a stable context was associated with an asymptotic increase in self-reported automaticity, with large individual variation. Limit: Ninety-six volunteers, self-selected eating, drinking or activity behaviours and self-reported automaticity; no universal 21-day or fixed-day habit guarantee and no proof that automaticity equals beneficial adherence.
03 · MOD-STRESS-RECOVERYCANDIDATE · UNSCORED
Self-Regulation & Sustainable Performance
Stress Recovery & Performance Under Pressure
Maintain a defined task standard and return toward a personal baseline after a consented, bounded, nonclinical performance stressor.
Does not establish
No universal resilience, nervous-system reset, trauma treatment, anxiety treatment or immunity from stress. Meditation is not required. Clinical exposure therapy, flooding, humiliation and uncontrolled high-stakes stress are outside scope.
Direct
Predeclare an objective task-performance score under a bounded stressor and a recovery endpoint. Recovery time is measured from stressor end to the first sustained return within the person's predeclared baseline band using a non-diagnostic indicator such as task readiness, a simple rating, or optional device data.
Retention
Repeat the same bounded stressor and task after at least 7 days without live coaching; retain the original performance and recovery criteria.
Transfer
Use a predeclared different but equally low-risk performance stressor or context, never a more severe clinical exposure.
Burden
Peak distress, delayed distress, sleep disruption, pain, fatigue, autonomic symptoms, device burden, avoidance, shame and time to recover.
Protocol and evidence gates
Select one nonclinical performance task and obtain explicit consent for a bounded, reversible stressor.
Record rested task performance, a personal recovery band, current readiness and all stop conditions.
Run one baseline stressor session at the lowest meaningful intensity and record performance, recovery and delayed burden.
Choose one narrow strategy: stress-arousal reappraisal, a rehearsed pre-performance plan, or optional paced-breathing/HRV biofeedback within medical and device constraints.
Practise only at a tolerable dose; increase complexity only when the prior dose caused no concerning immediate or delayed response.
Repeat the matched direct test, then complete delayed retention and the predeclared equally safe transfer context.
Route clinical anxiety, trauma, panic, dissociation, severe autonomic symptoms or functional deterioration to qualified care.
L1A consented baseline exists, but task performance or recovery is inconsistent, or substantial support is required.
L2Performance or recovery improves under the practised bounded stressor with active coaching or a tightly controlled setting.
L3The task-performance floor and recovery ceiling are met in two bounded sessions with no stop-rule breach or concerning delayed effect.
L4The L3 result survives delayed retest and the predeclared criterion is met under an equally safe novel performance context.
L5Performance and recovery remain reliable across at least three consented nonclinical constraints, and the person can explain a safe personal protocol without delivering therapy or prescribing exposure to others.
Safety, clinical, jurisdiction and accessibility guardrails
safety
No forced public performance, humiliation, deception, sleep deprivation, pain challenge, breath holding, hyperventilation or physical danger.
Stop immediately for chest pain, fainting, severe breathlessness, new neurological symptoms, dissociation, panic escalation or any participant withdrawal of consent.
Wearable HRV and pulse data are optional, non-diagnostic and never override symptoms or clinical advice.
clinical
Known trauma, panic disorder, severe anxiety, significant autonomic or cardiac symptoms, recent crisis or clinical exposure goals require qualified professional oversight.
This module does not replace CBT, exposure therapy, medication review or emergency mental-health care.
If symptoms persist outside the task or daily function worsens, pause and seek appropriate professional support.
jurisdiction
Public, workplace and educational simulations require informed consent, a safe opt-out and compliance with equality, safeguarding and employment rules.
Biometric data collection must meet applicable health-data, privacy and device requirements.
accessibility
Use equivalent performance contexts that do not require standing, speaking, vision, hearing or a specific motor response unless that function is the declared target.
Allow remote, seated, text-based, AAC and support-person routes and longer recovery windows.
Do not interpret autonomic differences, disability-related recovery time or use of an accommodation as lower capability when the declared function is preserved.
Promotion gates
Independent clinical-safety review must approve the consumer/clinical boundary and stop rules.
The Universal Module Lab must separate task performance, recovery, delayed burden and optional physiology.
Pilot participants must be able to withdraw without penalty and all stressors must be reversible and nonclinical.
Demonstrate that L4 transfer never means increasing stressor severity.
Publish an adverse-event and delayed-effect review rule before promotion.
Across 44 effect sizes, stress-arousal reappraisal and stress-is-enhancing interventions produced a small average improvement in task performance (d = 0.23). Limit: Moderate heterogeneity, mostly young nonclinical samples and evidence of publication asymmetry; trim-and-fill reduced the estimate to d = 0.14 and the prediction interval included negative effects.
A brief arousal-reappraisal instruction improved mathematics performance in a specific GRE-related testing context relative to control. Limit: Narrow test-performance setting and limited sample; does not establish universal academic improvement, anxiety treatment or safe self-directed clinical exposure.
HRV biofeedback was associated with reductions in self-reported stress and anxiety across included studies. Limit: Study quality, populations and protocols varied; self-reported symptom change does not prove improved task performance, faster recovery, diagnosis or suitability for people with cardiac or autonomic conditions.
Clinical social anxiety requires recognised assessment and treatment pathways; exposure is situated within structured psychological treatment rather than a generic consumer performance drill. Limit: Clinical guidance, not evidence that Titan's nonclinical module treats anxiety; jurisdiction is England and recommendations must be applied by appropriate professionals. Published 22 May 2013; last reviewed 21 May 2024. The stable evidence ID retains its original 2024 suffix for compatibility.
Information Verification, Provenance & Manipulation Resistance
Evaluate the source, provenance, corroboration and manipulation tactics of bounded information items using an auditable process before accepting, sharing or acting on them.
Does not establish
No lie detection, mind reading, universal scam immunity, real/fake certainty, political truth score or authority-by-brand. Correct source evaluation does not by itself establish that every claim from that source is true.
Direct
Accuracy on a balanced, answer-keyed set of unfamiliar items, with false-accept and false-reject rates reported separately; completion of an auditable provenance trace; and time to decision. The answer key must be independent of the learner.
Retention
After at least 14 days, use a new balanced item set with no repeated exemplars and the same scoring rule.
Transfer
Predeclare a different modality or threat class, such as article-to-image, source-to-claim, ordinary web source-to-authorised phishing simulation, or familiar-domain-to-unfamiliar-domain.
Burden
Verification time, false distrust, missed legitimate communication, exposure to disturbing material, privacy leakage, tool cost and escalation to professional review.
Protocol and evidence gates
Define the item class, decision stakes, balanced answer key and permitted verification tools before testing.
Record a blinded baseline on unfamiliar items and separate source credibility from claim accuracy.
Train a compact workflow: pause; identify the original source; read laterally; seek independent corroboration; inspect provenance or metadata where appropriate; and state residual uncertainty.
Practise recognising bounded manipulation techniques without using a single visual cue or brand as proof.
Use only inert, authorised phishing simulations; never open live suspicious attachments, run unknown code or submit credentials.
Retest on a nonrepeating balanced set after the delay, then run the predeclared cross-modality or cross-threat transfer.
Escalate medical, legal, financial, safety, identity and high-impact decisions to qualified or authoritative verification.
L1A blinded baseline exists, but decisions are inconsistent, provenance is missing or substantial support is required.
L2Accuracy and provenance improve on a practised item class with checklists, prompts or guided search.
L3The predeclared direct benchmark is met on unfamiliar items with false accepts and false rejects reported and no unsafe action.
L4The result survives a nonrepeating delayed set and meets the predeclared criterion in a novel modality, domain or authorised threat class.
L5Performance remains reliable across at least three declared modalities or threat classes and an independent benchmark; the person can teach the verification workflow while preserving uncertainty and avoiding claims of scam immunity.
Safety, clinical, jurisdiction and accessibility guardrails
safety
Use inert replicas, screenshots, isolated samples or authorised simulations; never interact with live malware, suspicious attachments or credential-harvesting pages.
Do not dox, harass, impersonate, entrap or publicly accuse a person as part of verification practice.
Use content warnings and stop rules for graphic, hateful, sexual, traumatic or personally targeted material.
clinical
This module does not validate paranoia, delusional certainty or compulsive checking.
If verification practice intensifies fear, surveillance behaviour, inability to disengage or fixed persecutory beliefs, pause and seek qualified support.
No mental-health diagnosis or lie-detection inference may be made from a person's information choices.
jurisdiction
Phishing simulations require explicit organisational authorisation, a nonpunitive design and compliance with computer-misuse, interception, employment and privacy law.
Respect copyright, data protection, defamation, platform terms and evidentiary rules.
The module is not legal, financial, medical or forensic certification.
accessibility
Provide screen-reader compatible pages, transcripts, captions, alt text, keyboard access and nonvisual provenance routes.
Allow extra time, reduced item sets and assistive search without weakening the declared decision standard.
Do not rely on colour, audio, facial expression, spelling or visual polish as the sole trust cue.
Promotion gates
Create balanced, independently keyed benchmark sets with documented provenance and no partisan or brand-based shortcut.
Validate false-accept, false-reject, uncertainty and trace-completeness scoring in the Universal Module Lab.
Authorised phishing simulations must pass legal, privacy, security and nonpunitive review.
Add evidence or narrow the transfer claim for synthetic image, audio and video provenance before those modalities can count toward L4 or L5.
Test for increased false distrust and compulsive checking as adverse outcomes.
Instruction in civic online reasoning, including lateral reading, improved university students' evaluation of online sources in the studied tasks. Limit: Educational tasks and student population; no proof of durable cross-domain scam resistance, synthetic-media detection or correct judgement in every live case.
Students in treatment classrooms improved more than controls in evaluating digital content after a classroom lateral-reading intervention. Limit: High-school government-course context with teacher professional development; transfer to adults, other domains, high-stakes decisions and long retention requires direct testing.
Three longitudinal experiments found that an active misinformation-inoculation game could improve resistance to tested misinformation techniques beyond an immediate posttest. Limit: Effects depend on item design and can decay; judging a technique or headline is not equivalent to verifying source provenance or resisting every manipulation in the wild.
Embedded anti-phishing education was evaluated with behavioural phishing decisions, including retention and transfer to novel phishing examples. Limit: Older email and web threat patterns; authorised research setting; results do not establish immunity to current adversarial attacks, and live phishing simulation raises legal, privacy and security requirements.
05 · MOD-FIRST-AID-READINESSCANDIDATE · UNSCORED
Making, Tool Use & Operations
First-Aid & Emergency Readiness
Recognise an emergency, activate the correct local response and perform one declared lay-responder skill set in standards-concordant simulation using a manikin, trainer or validated scenario.
Does not establish
No diagnosis, treatment licence, guaranteed survival, real-patient experimentation, advanced life support, invasive procedure or replacement for emergency dispatch. A Titan level is not a first-aid or CPR certificate.
Direct
Use the current pass criteria of a recognised jurisdiction-appropriate course or independent assessor. For CPR/AED, record instrumented compression rate, depth, recoil, hands-off time where available, AED-trainer sequence and emergency-call sequence. For other first-aid targets, use a validated scenario checklist with critical errors defined in advance.
Retention
Repeat an uncoached instrumented or independently observed assessment at 90 days. If the recognised provider requires a shorter interval, use the shorter interval.
Transfer
Complete a predeclared unfamiliar but standards-concordant scenario with changed location, bystander complication or equipment layout, using only manikins, trainers and simulation.
Burden
Pain, fatigue, dizziness, injury risk, emotional distress, equipment and course cost, accessibility barriers, time, infection-control burden and confidence–competence mismatch.
Protocol and evidence gates
Choose a jurisdiction, population and declared scope, such as adult compression-only CPR/AED, full basic life support, choking response or one recognised first-aid unit.
Record local emergency numbers, dispatcher role, consent boundaries and current recognised guidance.
Complete training through a recognised provider or qualified instructor using manikins, AED trainers and inert equipment.
Run an immediate independent or instrumented assessment and record every critical error, not only a total score.
Schedule brief refreshers and an uncoached 90-day retention assessment; mark the Titan level historical if the review window or certification expires.
Run one unfamiliar standards-concordant simulation for transfer, including activation of emergency services and safe scene assessment.
In any real emergency, contact the local emergency service promptly and follow dispatcher and qualified-responder instructions.
L1A safe simulated baseline exists, but recognition, sequencing or psychomotor performance is inconsistent or requires substantial prompting.
L2The practised sequence improves with instructor prompts, real-time feedback or a familiar scenario.
L3The current recognised direct assessment is passed for the declared scope with no critical error.
L4The assessment is passed uncoached at the required delayed interval and the unfamiliar standards-concordant simulation meets its predeclared criterion.
L5A current independent assessment or recognised certification confirms robust performance across at least three safe simulated constraints. Instructor status is not required and is never inferred.
Safety, clinical, jurisdiction and accessibility guardrails
safety
Use manikins and AED trainers; never practise chest compressions, abdominal thrusts, airway manoeuvres, tourniquets, injections or electrical shock on a live person.
Do not delay calling emergency services to complete a Titan checklist or collect data.
Stop for pain, dizziness, faintness, breathlessness, autonomic symptoms, injury or emotional distress; use a qualified instructor and appropriate infection control.
clinical
The module teaches response sequences, not diagnosis or medical treatment.
People with physical, cardiac, autonomic, musculoskeletal, pregnancy-related or trauma constraints should obtain appropriate professional advice before psychomotor practice.
Actual emergencies are governed by emergency dispatch and qualified responders, not the Titan level.
jurisdiction
Use current local emergency numbers, recognised guidance, scope-of-practice rules and certification requirements; Good Samaritan and duty-to-act rules vary.
A Titan record must never be represented as statutory, workplace or professional certification.
Training providers, instructors and equipment must meet applicable local requirements.
accessibility
Define accessible responder roles such as recognising the emergency, calling dispatch, retrieving an AED, directing bystanders, communicating history or guiding access.
Credit only the role actually demonstrated; an accessible communication role does not silently become a CPR psychomotor pass.
Provide seated, visual, auditory, tactile, AAC and support-person routes and accessible equipment where recognised by the relevant standard.
Promotion gates
Map at least UK/ERC and US/AHA lay-responder pathways without merging conflicting jurisdictional requirements.
Require recognised-provider or independent-assessor criteria for L3 and L5; Titan cannot self-certify.
Validate instrumented-manikin and scenario-checklist import fields in the Universal Module Lab.
Add narrow evidence and critical-error definitions for every non-CPR first-aid exemplar before it is scoreable.
Complete clinical, physical-access, safeguarding, infection-control and legal review before promotion.
Current AHA education guidance recommends CPR feedback devices during skills training and supports evidence-based approaches to acquisition, mastery and retention. Limit: Clinical guideline and US framework; it does not make Titan a training provider, establish certification or guarantee real-event survival from a simulator score.
Real-time visual feedback improved instrumented CPR skill acquisition and retained an advantage at 10 and 28 weeks in high-school students; the difference was no longer significant at 52 weeks. Limit: Compression-only simulation in students, not actual cardiac arrests or a complete first-aid curriculum; the result demonstrates both measurability and decay, not guaranteed real-world action.
ERC guidance addresses education, simulation, feedback, skill maintenance and assessment from basic through advanced resuscitation. Limit: European framework whose requirements must be checked against the current local 2025 guidance and recognised provider; not a Titan certification standard by itself.
ERC provides evidence-informed first-aid recommendations across a bounded set of emergency conditions and interventions. Limit: Recommendations are condition- and jurisdiction-specific, change over time and do not supply one universal first-aid performance score; each scoreable exemplar needs current critical-error criteria.
06 · MOD-SLEEP-REGULARITYCANDIDATE · UNSCORED
Self-Regulation & Sustainable Performance
Sleep Regularity & Recovery
Measure and improve the stability of one personally feasible sleep–wake schedule under declared conditions while preserving adequate sleep opportunity and daytime safety.
Does not establish
No diagnosis or treatment of insomnia, sleep apnoea, circadian-rhythm disorder, shift-work disorder or another clinical condition. No CBT-I, stimulus control, sleep-restriction therapy, forced phase shifting, all-nighters, sleep deprivation, polyphasic sleep compression, medication or supplement changes, light therapy, universal bedtime or chronotype claim.
Direct
Predeclare one primary regularity measure and retain it throughout the protocol: Sleep Regularity Index calculated from complete time-stamped sleep/wake states; diary-derived day-to-day sleep-onset and wake-time variability; or actigraphy-derived Sleep Regularity Index. Record measurement mode, epoch, valid-day rule, missing-data rule and a sleep-duration or sleep-opportunity safety floor before baseline. Diary-derived metrics are self-recorded; actigraphy-derived metrics are instrumented. Sleep efficiency may be recorded as a secondary descriptive measure only and cannot be optimized by reducing time in bed.
Retention
Repeat the same measurement mode across a new 14-day window at least 30 days after the supported phase, without live coaching and using only the predeclared maintenance supports.
Transfer
When a naturally occurring, low-risk schedule change occurs, test whether the predeclared regularity and sleep-opportunity criteria remain satisfied or are safely re-established. Never create travel, shift work, sleep loss or another disruption solely to test transfer.
Burden
Tracking time, device cost, alarm burden, anxiety or orthosomnia, daytime sleepiness, missed obligations, conflict with pain, disability, caregiving, work, culture or chronotype, and any safety-critical error or near miss.
Protocol and evidence gates
Screen for dangerous daytime sleepiness, persistent insomnia symptoms, suspected apnoea, shift-related impairment, recent mania or another condition requiring professional assessment.
Choose one personally feasible schedule and one primary regularity metric; record whether evidence is self-recorded or instrumented.
Collect at least 14 consecutive baseline days without reconstructing missing nights from memory. A Sleep Regularity Index requires sufficiently complete sleep/wake-state data, including declared naps.
Predeclare the regularity target, valid-day and missing-data rules, sleep-opportunity floor, daytime-safety indicators and stop conditions.
Choose one ordinary nonclinical scheduling support, such as a calendar buffer, wind-down reminder, morning routine cue or better placement of obligations. Do not restrict sleep opportunity or change medication, supplements, light treatment or clinical equipment.
Run two comparison windows and retain, adapt or stop the support based on regularity, preserved sleep opportunity, daytime function and burden.
Repeat the 30-day delayed window and wait for a naturally occurring safe schedule change before attempting the transfer test.
L1A baseline exists, but the record is incomplete, the schedule is unstable or daytime safety and sleep opportunity have not been protected.
L2Regularity improves under the practised conditions with active reminders or substantial support, while the safety floor remains intact.
L3The predeclared direct criterion is met in two consecutive complete windows without reducing sleep opportunity, worsening daytime sleepiness or crossing a stop rule.
L4The result survives the delayed window and the criterion is safely maintained or re-established during a naturally occurring schedule change.
L5Performance remains reliable across at least three naturally occurring constraints over the review period, with an independently reviewed record and an accurate explanation of the measurement and clinical boundaries.
Safety, clinical, jurisdiction and accessibility guardrails
safety
No sleep restriction, deprivation, all-nighter, forced wakefulness or radical polyphasic schedule may be used.
Do not drive, cycle, operate machinery, supervise a dependent person or perform safety-critical work when dangerously sleepy.
Stop for severe sleepiness, confusion, faintness, a safety-critical error, a near miss or material deterioration in daytime function.
Current or recent mania, psychosis, suicidal crisis or clinically significant deterioration requires professional care rather than schedule experimentation.
CBT-I, stimulus control, sleep-restriction therapy, medication, melatonin, light therapy and CPAP or other device changes remain clinician governed.
jurisdiction
Workplace fatigue-management, working-time, transport and safety rules override a Titan protocol.
Sleep records are sensitive health and employment data and must not be used for coercive monitoring, discipline or discrimination.
A Titan record is not medical clearance or proof of fitness for work, driving or duty.
accessibility
Treat chronotype, disability, pain, nocturnal care, religious practice, split sleep, night work and caregiving as design constraints rather than moral failure.
Permit diaries, accessible digital logs, support-person entries or optional wearables, while preserving the evidence-mode label and not pretending the modes are identical.
Stop or simplify tracking if it causes compulsive checking, sleep anxiety or orthosomnia.
Promotion gates
Validate the Sleep Regularity Index implementation against published examples and specify the epoch, completeness and missing-data rules.
Prove that missing nights, omitted naps or reduced sleep opportunity cannot improve the score.
Establish an interpretable minimum-change or criterion policy before any level becomes scoreable; do not invent a universal SRI pass mark.
Keep diary-derived results labelled self-recorded and actigraphy-derived results labelled instrumented throughout the Cockpit and exports.
Independent sleep-clinical review must approve the insomnia, apnoea, shift-work, mania and dangerous-sleepiness routing.
Pilot a no-wearable route and test accessibility with pain, disability, caregiving, neurodivergence and nonstandard schedules.
Monitor daytime sleepiness, safety incidents and orthosomnia as adverse outcomes.
Confirm that retention and transfer never require an induced sleep disruption.
In 61 undergraduates followed for 30 days, the authors defined the Sleep Regularity Index as the probability of being in the same sleep/wake state at time points 24 hours apart and found associations with circadian timing and academic performance. Limit: Observational, small and undergraduate-specific; it cannot establish causality. The study used sleep diaries, so those SRI data were self-recorded rather than objective.
An expert- and patient-informed process produced a standard core diary for prospective sleep self-monitoring. Limit: The publication calls the diary a living document requiring further testing and validation. Diary variables, including diary-derived sleep efficiency, remain self-recorded.
Among 40 adolescents with analyzable actigraphy, the intervention reduced weekend–weekday sleep-onset discrepancy by 54 minutes and the increased regularity was maintained at the next study period. Limit: Small sample aged 13–15, clinician session, secondary outcomes and short follow-up; total sleep time did not significantly change.
The guideline places multicomponent CBT-I and components including sleep-restriction therapy within clinical treatment of chronic insomnia and suggests not using sleep hygiene alone as treatment. Limit: Clinical guideline for adults with chronic insomnia, not evidence that a consumer regularity protocol treats insomnia.
Provides consensus context for protecting adequate sleep duration in healthy adults. Limit: Population-level guidance for healthy adults, not an individual prescription and not a regularity intervention.
After retaining 22 relevant papers, the panel found no evidence supporting benefits of radical polyphasic schedules and advised against schedules that substantially reduce or fragment sleep. Limit: Consensus review supporting an exclusion and Observatory caution, not a regularity-training efficacy study.
Select, standardise and track one low-risk, instrument-defined aspect of functional capacity, such as grip, sit-to-stand performance, basic mobility or an approved submaximal walking test. Titan measures performance and change; it does not prescribe exercise, rehabilitation, intensity, dose or progression.
Does not establish
No diagnosis, medical clearance, rehabilitation plan, fitness programming, maximal or exhaustion testing, pain challenge, fall challenge, weight-loss claim, universal fitness score or proof of occupational, sporting or military readiness.
Direct
Use one validated test and its fixed protocol: kilograms or newtons for grip dynamometry; completed repetitions for a specified chair-stand test; seconds and observed critical errors for Timed Up & Go; or distance for an appropriately supervised submaximal walking test. Record device, chair height, footwear, assistive aid, assistance, course, assessor, time and symptom state. Do not aggregate incompatible tests into a universal score.
Retention
Repeat the identical protocol after at least 28 days, using the same accommodations and no extra warm-up or assistance beyond the predeclared standard.
Transfer
Complete a predeclared second validated measure or functional task selected by a qualified assessor as relevant to the same real-world function. Transfer must be measured directly and cannot be inferred from the first test.
Burden
Pain, fatigue, breathlessness, dizziness, falls or near misses, glucose disruption, delayed symptom worsening, equipment and assessor cost, space, transport, assistance and recovery time.
Protocol and evidence gates
Define the functional question and select one validated measure appropriate to the person's age, condition, access needs and risk.
Obtain professional clearance when fall, fracture, cardiovascular, respiratory, neurological, metabolic, autonomic, pregnancy-related, postsurgical or significant pain risk is present.
Lock the published protocol, equipment, environment, assistance, assistive device, assessor and stop rules before testing.
Run a safe familiarisation if the published protocol permits it, then collect the witnessed or instrumented baseline and every symptom or critical error.
If the person undertakes training or rehabilitation, that plan remains separately governed by the appropriate professional; Titan records outcomes only.
Retest with the identical protocol, then complete the delayed retest.
Use a separately approved related measure for transfer and report agreement or disagreement rather than manufacturing a combined score.
L1A safe baseline is incomplete, inconsistent or requires substantial support, or the protocol and accommodations are not yet standardised.
L2The declared test is completed safely and consistently with support, familiarisation or active feedback.
L3The current external or predeclared test-specific direct criterion is met in two witnessed sessions with no critical error or stop-rule breach.
L4The result survives the delayed retest and the separately measured related task meets its predeclared criterion.
L5An independent qualified assessor confirms sustained performance across at least two validated measures and declared constraints, without implying global fitness, diagnosis or authority to prescribe.
Safety, clinical, jurisdiction and accessibility guardrails
safety
No maximal lift, exhaustion test, deliberate fall, unsupported balance challenge, pain challenge or test-to-failure is permitted.
Stop immediately for chest pain, severe breathlessness, faintness, new neurological symptoms, acute pain, loss of balance, unsafe glucose state or participant withdrawal.
Use a spotter, rails, usual assistive device and clinical setting whenever the selected protocol or individual risk requires them.
clinical
Recent fracture, surgery, fall, cardiac or respiratory event, progressive neurological change, significant autonomic symptoms, unstable diabetes, pregnancy-related risk or unexplained functional decline routes to qualified assessment.
Test results do not diagnose frailty, sarcopenia, cardiovascular disease, neurological disease or fall risk outside the validated use of the selected instrument.
Rehabilitation and exercise dose, progression and contraindications remain professionally governed.
jurisdiction
Occupational, sporting, driving, insurance and statutory fitness standards remain controlled by their authorised bodies.
A Titan level is not medical clearance, workplace certification or a professional fitness qualification.
Physical and health data must be handled under applicable privacy, equality and employment rules.
accessibility
Use a measure that tests the declared function rather than penalising a person for being unable to stand, walk, grip or see when that function is not the intended target.
Record chair height, prosthesis, orthosis, wheelchair, walking aid, communication support and human assistance, and keep them identical across comparisons where feasible.
Do not compare results across incompatible devices, body positions, chair heights, course lengths or assistance conditions.
Promotion gates
Publish an instrument pack for every accepted test containing the exact protocol, intended population, units, contraindications, critical errors, test–retest evidence and acceptable change rule.
Prove that equipment, chair height, assistance, course length, device substitution and practice effects cannot silently inflate a level.
Require witnessed or independently assessed evidence for L3 and L5; self-report alone cannot pass.
Clinical and accessibility review must cover falls, fractures, cardiac, respiratory, neurological, metabolic, autonomic, pain and wheelchair-access routes.
Demonstrate that the module never generates exercise or rehabilitation programming.
Validate a transfer rule that measures a second function directly and never infers global fitness.
Resolve the family-placement question before promotion.
Pilot across different ages and ability levels without transporting population-specific norms into unsupported groups.
In 76 community-dwelling adults over 60, test–retest reliability was 0.84 for men and 0.92 for women, with correlations of 0.78 and 0.71 with weight-adjusted maximum leg press. Limit: Generally active older adults and a fixed chair/protocol; results do not establish universal norms or validity under altered setup.
In 60 geriatric day-hospital patients, the timed test showed inter- and intra-rater reliability and correlated with balance, gait speed and activities-of-daily-living measures. Limit: Frail older clinical sample; it is not a universal fitness test or stand-alone proof of safe independent mobility.
The study combined 60,803 observations from 49,964 participants aged 4 to 90 across 12 British population studies to produce grip-strength centiles. Limit: Cross-sectional British data; centiles are reference distributions rather than diagnoses, and protocol/device comparability must be preserved.
In more than 5,000 adults aged 71 and older, the lower-extremity battery characterised function and added predictive information beyond self-report. Limit: Older-adult observational cohorts; association is not intervention efficacy and the battery does not represent every population or high-performance domain.
Provides a standardised clinical protocol for administering the six-minute walk test. Limit: Clinical submaximal test requiring its safety and procedural conditions; not a general unsupervised endurance challenge.
External Anchor Ledger · candidate
Third-party evidence without Titan grading itself.
These 14 issuing-authority or primary-instrument routes are proposed evidence anchors. Each still carries scope, recency and verification limits.
Council of Europe CEFR plus the independent examination provider
A component-scored language examination whose provider publishes a transparent procedure for relating the examination to CEFR levels A1-C2. A CEFR self-assessment grid is not an independently assessed result.
Verification and boundary
Verify: Verify the certificate or statement of results through the issuing examination provider, including level, skill components, date and candidate identity; record the provider’s published CEFR-linking method.
Recency: The CEFR framework has no universal certificate-expiry rule. Record the test date and provider policy; Titan must require current-use or retest evidence when the result is too old for the claimed current capability.
Limit: The Council of Europe defines six levels and descriptors but explicitly does not verify or validate the quality of an examination provider’s claimed CEFR linkage. Provider quality and skill coverage therefore require separate approval.
American Heart Association authorized Training Center
Successful completion of an appropriate AHA ECC course, such as Heartsaver First Aid CPR AED, evidenced by an issuer-controlled course-completion eCard.
Verification and boundary
Verify: Enter the eCard code or scan its QR code on the AHA My Cards verification service; printed cards may also be checked with the issuing Training Center.
Recency: AHA course-completion cards are valid for two years through the end of the issue month.
Limit: The card proves successful completion of the named course, not current real-emergency performance. Skill decay, course scope, local first-aid rules and recertification requirements remain relevant.
Driver and Vehicle Standards Agency via the official Great Britain car theory test
The hazard-perception component of the official car theory test, scored out of 75 with a current pass mark of 44. The full theory test is passed only when both the multiple-choice and hazard-perception parts are passed.
Verification and boundary
Verify: Witness or retain a redacted copy of the official result letter showing the hazard-perception score and test date. Treat the pass-certificate number as sensitive and do not publish it.
Recency: The official theory-test pass certificate number lasts two years for booking and taking the practical driving test. Record the test date and the contemporaneous pass threshold.
Limit: This is an external screen-based driving assessment, not evidence of on-road safety, eyesight, licensing status or general sensorimotor capacity. The pass mark and process can change and require a release-currentness check.
US Centers for Disease Control and Prevention STEADI
Thirty-second Chair Stand using a straight-backed 17-inch chair without armrests and a stopwatch, with the number of full stands scored under the published protocol.
Verification and boundary
Verify: A trained witness follows the CDC sheet, stays next to the participant for safety and signs the dated score record. Video is optional only with informed consent and secure handling.
Recency: No certificate or issuer expiry. Record assessment date, time, chair height, footwear, assistance and symptoms; repeat only on the approved clinical schedule.
Limit: CDC presents this as a test of leg strength and endurance within older-adult fall-risk assessment. It is not a diagnosis, universal fitness norm or unsupervised challenge; the sheet directs the assessor to stay next to the patient.
US Centers for Disease Control and Prevention STEADI
Timed Up & Go using a standard armchair, a marked line three metres or ten feet away, regular footwear and the participant’s usual walking aid when needed; time stops after the participant sits again.
Verification and boundary
Verify: A trained witness follows the CDC protocol, remains beside the participant for safety and signs the dated time-and-observation record.
Recency: No certificate or issuer expiry. Record date, conditions, walking aid, symptoms and observations; reassessment interval belongs to the clinician-approved plan.
Limit: CDC states that an older adult taking at least twelve seconds is at risk for falling. This threshold is a screening signal, not a diagnosis or general fitness grade, and neurological or gait observations can require further evaluation.
Consensus Sleep Diary expert group; published in SLEEP
The Core Consensus Sleep Diary, a standardized prospective self-monitoring instrument from which declared timing, continuity and sleep-efficiency measures can be derived.
Verification and boundary
Verify: Retain a dated diary export or redacted sheet with item completeness and formula checks. Independent witnessing is optional and must not expose unnecessary health information.
Recency: No certificate expiry. Record a dated contiguous window; the candidate module must predeclare the minimum valid-night count and cannot recycle an old window as current evidence.
Limit: The publication describes an expert-consensus, patient-informed standardized diary and explicitly calls it a living document needing further testing, refinement and validation. It is not a sleep-disorder diagnosis or an objective sleep measure.
American Academy of Sleep Medicine clinical practice guideline
Clinician-directed actigraphy used to estimate sleep parameters under an applicable AASM recommendation, with the device, algorithm, wear interval and diary pairing documented.
Verification and boundary
Verify: Use the clinician’s dated report or a redacted device export reconciled to the prescribed wear and diary protocol; retain device and algorithm metadata.
Recency: No certificate expiry. Preserve the exact observation interval, device and scoring algorithm; a later claim requires a new representative interval under the clinical plan.
Limit: The AASM recommendations are for clinicians evaluating suspected or diagnosed sleep or circadian disorders and are mostly conditional. The guideline applies to FDA-approved devices and does not make a general consumer-wearable or self-diagnosis claim.
A public or independently verified user track record computed from quantified forecasts after questions resolve, using the platform’s current Baseline, Peer or tournament scoring method.
Verification and boundary
Verify: Verify the public profile or platform export, resolved-question count and score fields. Preserve a dated, tamper-evident export because scoring systems and displayed fields can change.
Recency: The platform has no credential expiry. Record the export date, scoring version, number and type of resolved questions and most recent resolution; Titan must set the recency and sample thresholds before promotion.
Limit: Metaculus states that scores measure performance over many predictions and currently uses Baseline and Peer scores, with Relative scores retained for tournaments. Scores depend on question mix, participation and the active scoring method; a rank or medal alone is insufficient.
National Restaurant Association Educational Foundation ServSafe; ANAB-Conference for Food Protection accredited examination
ServSafe Food Protection Manager Certification earned through the proctored accredited examination and verified through the issuer’s certificate service.
Verification and boundary
Verify: Use the ServSafe Validate a Certificate service or issuer account record and record certificate type, issue date, current validity and jurisdiction without publishing the full credential number.
Recency: Verify the certificate’s current validity and the applicable local regulatory requirement at assessment time; do not apply a universal Titan expiry where the issuer or jurisdiction differs.
Limit: The official program states that the Manager examination is ANAB-CFP accredited and nationally accepted, but a knowledge certification is not a witnessed knife, heat, allergen-control, fold-quality or kitchen-workflow assessment.
National Navigation Award Scheme approved provider
Bronze National Navigation Award, verified through the approved provider and restricted to the named outdoor-navigation outcomes.
Verification and boundary
Verify: Verify provider approval, participant result, award level and assessment date with the issuing provider while withholding unnecessary certificate identifiers.
Recency: The award has no universal Titan currentness period. Record assessment date and require current retained/transfer evidence for a current Titan claim.
Limit: This is outdoor land-navigation evidence, not proof of all Spatial Representation outcomes, urban mobility, traffic safety, wilderness leadership or independent travel without appropriate aids.
National Navigation Award Scheme approved provider
Gold Navigator Award, verified through the approved provider and restricted to the named advanced outdoor-navigation outcomes.
Verification and boundary
Verify: Verify provider approval, participant result, award level and date with the issuing provider and retain only necessary credential data.
Recency: Record the assessment date and require current retained/transfer evidence for a current Titan claim.
Limit: The award does not establish every spatial task, universal wilderness competence, leadership qualification or safe navigation without required equipment and local judgment.
A named Adult Distance Award witnessed and recorded through a Swim England programme provider.
Verification and boundary
Verify: Verify the award level and date with the provider and record the exact witnessed outcome without retaining unnecessary personal identifiers.
Recency: Record the date, pool conditions, stroke and distance. A historical award is not current swimming evidence without a safe current reassessment.
Limit: Adult awards may be flexibly delivered. Do not infer technique, deep-water safety, rescue capability, open-water competence or a general fitness level.
RSPH Level 2 Award in Food Safety and Hygiene, verified through the issuing centre or awarding body.
Verification and boundary
Verify: Verify qualification title, awarding body, result and date through the issuer or centre while redacting full credential identifiers from public exports.
Recency: Verify current issuer status and any employer or jurisdiction-specific refresher requirement. Titan does not invent a universal expiry.
Limit: The assessment is knowledge-based. UK government guidance requires appropriate training and supervision but does not universally require every food handler to hold a certificate.
What must be true before candidate becomes capability.
Candidate status cannot promote itself. The Research & Governance Lab applies one explicit, human-governed promotion process across every research lane; this release records zero new promotions.
All evidence URLs resolve and every ledger claim and limitation receives independent editorial verification at release time.
Each module has a predeclared direct outcome, delayed-retention interval, novel-transfer rule, burden measure, stop rules and review window.
Level 3 cannot be earned from self-report alone; Level 4 requires both delayed retention and predeclared transfer; Level 5 requires robust constraints plus safe explanation, independent assessment or benchmark as the module specifies.
Not assessed remains blank and is never converted to L1 or zero.
No candidate contributes to a Core Score, global or layer composite, portfolio average, rank, automatic bottleneck or automatic programme recommendation.
Safety, clinical, jurisdiction and accessibility reviews pass for every worked example and every data field.
The Universal Module Lab rejects unsupported levels, records missing coverage and keeps candidate data separate from promoted-module exports.
At least one adversarial test proves that each direct measure cannot be passed by lowering task quality, omitting difficult opportunities, selecting only easy items or increasing risk.
A migration test confirms that earlier exports import without inventing assessments for any candidate module.