Right to Cognitive Integrity

1. Hypothesis

A transparent, safety-bounded and person-centred approach to right to cognitive integrity, combining validated measurement, informed consent, privacy and security controls, human oversight and longitudinal monitoring, will improve benefit–risk outcomes compared with opaque or technology-centred approaches.

2. Experiment design

Design: rights-centred mixed-method study using controlled scenarios, stakeholder deliberation and comparative legal analysis focused on Right to Cognitive Integrity Methods: rights analysis; scenario-based user studies; informed-consent testing; coercion and manipulation assessment; legal comparison; participatory research; ethics review; expert and affected-user review; reproducibility testing; methods adapted specifically to Right to Cognitive Integrity Independent variables: technology type; exposure or intervention intensity; duration; assurance controls; human oversight; user characteristics; operating context Dependent variables: functional outcome; biological or neural safety; user agency; privacy; reliability; recovery; subtopic-specific outcome for protection of cognitive functioning and mental continuity from unauthorised interference Confounders: age; health; disability; medication; prior experience; baseline physiology; environment; device quality; clinician or operator expertise; socioeconomic access Measures: perceived autonomy; informed refusal; coercion exposure; comprehension; reversibility; decisional capacity; procedural fairness; remedy access; validated subtopic measures for protection of cognitive functioning and mental continuity from unauthorised interference; subgroup effects; false-positive and false-negative rates; user-reported burden Success criteria: Statistically and clinically or practically meaningful benefit; acceptable adverse-event profile; preserved agency and privacy; no disproportionate subgroup harm; reproducible performance; explicit safety limits; effective recovery and human escalation. Failure conditions: No meaningful benefit; biological, neural, psychological, privacy or rights harm exceeds benefit; performance fails outside narrow conditions; unsafe dependency emerges; consent or refusal is compromised; incidents cannot be detected, reversed or remediated.

3. Seed result / current evidence

DEFENSIBLE SEED RESULT — NON-EMPIRICAL. The current evidence supports Right to Cognitive Integrity as a testable research proposition. Problem basis: Neurotechnology and AI-mediated persuasion may affect thought, attention, emotion and choice while existing rights frameworks do not always define enforceable boundaries. The specific unresolved issue is protection of cognitive functioning and mental continuity from unauthorised interference. Directional expectation: If supported, the proposed approach should improve functional outcome; biological or neural safety; user agency; privacy; reliability; recovery; subtopic-specific outcome for protection of cognitive functioning and mental continuity from unauthorised interference while reducing adverse effects, misuse, exclusion, dependency and recovery time. Proposed observations: perceived autonomy; informed refusal; coercion exposure; comprehension; reversibility; decisional capacity; procedural fairness; remedy access; validated subtopic measures for protection of cognitive functioning and mental continuity from unauthorised interference; subgroup effects; false-positive and false-negative rates; user-reported burden. Seed data profile: Evidence Strength 10/100; Confidence 25/100; Maturity 20/100; Overall Health 35/100; Novelty 80/100; Strategic Importance 95/100. Evidence boundary: No validated results yet.; experiments 0, studies 0, participants 0. This is suitable for protocol formation and baseline comparison, not as a finding of effect.

4. Seed conclusion

DEFENSIBLE SEED CONCLUSION — PROVISIONAL. Right to Cognitive Integrity warrants structured testing because the CSV identifies a defined problem, falsifiable hypothesis, measurable outcomes and relevant literature foundations. The present position is that “A transparent, safety-bounded and person-centred approach to right to cognitive integrity, combining validated measurement, informed consent, privacy and security controls, human oversight and longitudinal monitoring, will improve benefit–risk outcomes compared with opaque or technology-centred approaches.” is plausible and decision-relevant, but unvalidated. Proceed to controlled testing against the stated success and failure conditions. Confirm, narrow or reject this seed after effect sizes, uncertainty, subgroup outcomes, adverse effects, persistence and handback performance are observed.

Prior-art search performed before starting

PRIOR-ART SEED BASELINE — PARTIAL. The CSV records these literature domains: Neuroscience; neurotechnology; physiology; medical-device safety; rehabilitation; cybersecurity; bioethics; human rights; literature specific to Right to Cognitive Integrity. It also records: UN Universal Declaration of Human Rights — https://www.un.org/en/about-us/universal-declaration-of-human-rights; Council of Europe human rights and biomedicine — https://www.coe.int/; UNESCO Universal Declaration on Bioethics and Human Rights — https://www.unesco.org/; OECD AI Principles — https://oecd.ai/. Evidence register status: “Seeded; authoritative source register initiated; empirical evidence not yet ingested”. This is defensible as a starting prior-art inventory, but not as proof of a completed systematic search because search dates, databases, exact queries, reviewer, result counts, screening decisions, claim mapping and a replayable receipt are absent.

Prior-art material named: Existing literature: Neuroscience; neurotechnology; physiology; medical-device safety; rehabilitation; cybersecurity; bioethics; human rights; literature specific to Right to Cognitive Integrity. References: UN Universal Declaration of Human Rights — https://www.un.org/en/about-us/universal-declaration-of-human-rights; Council of Europe human rights and biomedicine — https://www.coe.int/; UNESCO Universal Declaration on Bioethics and Human Rights — https://www.unesco.org/; OECD AI Principles — https://oecd.ai/

Critical gap / next action

Create and attach a dated prior-art search log; lock the protocol; execute the proposed study; link raw data and analysis; then replace the results and conclusion placeholders with evidence-bounded findings.