Tests NESA microcurrent device for stroke aftereffects rehabilitation
Tests a non-invasive microcurrent device for spasticity, balance and pain in stroke survivors.
Plain-language title generated from the registry record
Registry title: Non-invasive Neuromodulation NESA Application in the Rehabilitation of Stroke Sequelae
Key facts
- Where
- Las Palmas de Gran Canaria, SpainSee the site
Where in Spain
- Mariola Lledó AmatLas Palmas de Gran Canaria, SpainTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- University of Las Palmas de Gran Canaria
- Trial code
- NCT05853952
- Record updated
- 5 May 2026
- Original description
To evaluate whether NESA microcurrents can be used as an effective treatment for various sequelae present in stroke patients, specifically in the treatment of spasticity, balance, pain; and whether it affects quality of life, performance of activities of daily living and quality of sleep.Read full original descriptionShow less
Non-invasive Neuromodulation NESA Application in the Rehabilitation of Stroke Sequelae. A Pilot Study
To evaluate whether NESA microcurrents can be used as an effective treatment for various sequelae present in stroke patients, specifically in the treatment of spasticity, balance, pain; and whether it affects quality of life, performance of activities of daily living and quality of sleep.
Inclusion: People who have suffered a stroke with an evolution between 6 months and 6 years; Optimal cognitive capacity and mentally competent to participate in the study and complete the required questionnaires; People able of standing upright, including those who need technical aids.
Exclusion: Present some of the contraindications for a treatment with NESA XSIGNAL®: pacemakers, internal bleeding, not to apply electrodes on skin in bad condition, with ulcerations or wounds, acute febrile processes, acute thrombophlebitis and/or phobia to electricity; Not having signed the informed consent form; Presenting any additional injury or pathology during the study; Not having the optimal cognitive capacities for understanding and participating in the study.