
NESA modulates the autonomic nervous system in chronic pain, neuropathies and neurorehabilitation — with measurable improvement in sleep and cognitive function.
Dysautonomia and autonomic balance
Like a miscalibrated control centre sending crossed signals. Dysautonomia is a direct imbalance between “gas” and “brake” — which is why symptoms shift from day to day.
Self-assessment, not self-diagnosis — discuss with a professional.
Reduced pain and a raised pain threshold without medication.
Improved sleep quality and cognitive function — including in dementia.
Support of recovery in neurological injury and neuropathies.
In dementia, NESA improves sleep, reduces daytime sleepiness and raises cognitive function.
Study results; individual results may vary. Information intended for healthcare professionals.
Low-frequency microcurrents (0.1–1 mA, 1–15 Hz), applied through the four limbs with a guiding electrode, engage the autonomic nervous system along its whole axis. Instead of suppressing a symptom, NESA restores the balance between the sympathetic and parasympathetic divisions — a state in which the brain consolidates sleep, modulates nociception and supports cognitive networks. That is why the effects accumulate across sessions and persist after the protocol, without habituation.
In neurology this is especially valuable where pain, disturbed sleep and autonomic dysregulation feed one another — in chronic and neuropathic pain, in dementia and in neurorehabilitation after injury.
The patient is at rest; electrodes are placed on the wrists and ankles and a guiding electrode according to the target. The session lasts ~55 minutes, painlessly. Standard protocol: 12–20 sessions, twice a week. The effect is monitored objectively through sleep and heart-rate variability.
Microcurrents through the wrists and ankles — the whole autonomic axis at once.
Pain, memory and sleep centres seeking a non-invasive complement.
Recovery after stroke, trauma and in polyneuropathies.
Improving sleep, daytime activity and cognition.
Indications, protocols, programmes and clinical data for implementing NESA in your practice.
Yes. NESA is a non-invasive, low-intensity method with no known systemic side effects. Sessions are conducted by a trained specialist.
No. NESA complements pharmacological treatment and rehabilitation by reducing pain and improving sleep — often allowing the physician to review dosages.
Many report better sleep after 4–6 sessions; the effect on pain and cognition builds over the full course.
Pacemakers and other active implants, pregnancy and epilepsy require prior medical assessment. When in doubt, consult the treating physician.
Source: NESA protocol handbook · INF-CD-022 (2025-V.1). Standard session 60 min, LOW mode by default.
Every protocol in this field combines the reference programmes P1–P9 — general homeostasis, body levels, ANS/CNS and targeted nerves — according to the clinical goal.
See programmes P1–P9 →Parameters are guides; the therapist adapts them to the patient.
NESA is not suitable for every patient and promises no cure.
Absolute contraindications (pacemaker, pregnancy, active implants) follow the device IFU.
The same numbers as above — in a ready-to-share format for colleagues, patients and social media.